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In recent years, many light-microscopy protocols have been published for visualization of nanoscale structures in the kidney. These protocols present researchers with new tools to evaluate both foot process anatomy and effacement, as well as protein distributions in foot processes, the slit diaphragm and in the glomerular basement membrane. However, these protocols either involve the application of different complicated super resolution microscopes or lengthy sample preparation protocols. Here, we present a fast and simple, five-hour long procedure for three-dimensional visualization of kidney morphology on all length scales. The protocol combines optical clearing and tissue expansion concepts to produce a mild swelling, sufficient for resolving nanoscale structures using a conventional confocal microscope. We show that the protocol can be applied to visualize a wide variety of pathologic features in both mouse and human kidneys. Thus, our fast and simple protocol can be beneficial for conventional microscopic evaluation of kidney tissue integrity both in research and possibly in future clinical routines.

Activation of the apoptotic pathway is a major cause of progressive loss of function in chronic diseases such as neurodegenerative and diabetic kidney diseases. There is an unmet need for an anti-apoptotic drug that acts in the early stage of the apoptotic process. The multifunctional protein Na+,K+-ATPase has, in addition to its role as a transporter, a signaling function that is activated by its ligand, the cardiotonic steroid ouabain. Several lines of evidence suggest that sub-saturating concentrations of ouabain protect against apoptosis of renal epithelial cells, a common complication and major cause of death in diabetic patients. Here, we induced apoptosis in primary rat renal epithelial cells by exposing them to an elevated glucose concentration (20mM) and visualized the early steps in the apoptotic process using super-resolution microscopy. Treatment with 10nM ouabain interfered with the onset of the apoptotic process by inhibiting the activation of the BH3-only protein Bad and its translocation to mitochondria. This occurred before the pro-apoptotic protein Bax had been recruited to mitochondria. Two ouabain regulated and Akt activating Ca2+/calmodulin-dependent kinases were found to play an essential role in the ouabain anti-apoptotic effect. Our results set the stage for further exploration of ouabain as an anti-apoptotic drug in diabetic kidney disease as well as in other chronic diseases associated with excessive apoptosis., QC 20210819

In recent years, many light-microscopy protocols have been published for visualization of nanoscale structures in the kidney. These protocols present researchers with new tools to evaluate both foot process anatomy and effacement, as well as protein distributions in foot processes, the slit diaphragm and in the glomerular basement membrane. However, these protocols either involve the application of different complicated super resolution microscopes or lengthy sample preparation protocols. Here, we present a fast and simple, five-hour long procedure for three-dimensional visualization of kidney morphology on all length scales. The protocol combines optical clearing and tissue expansion concepts to produce a mild swelling, sufficient for resolving nanoscale structures using a conventional confocal microscope. We show that the protocol can be applied to visualize a wide variety of pathologic features in both mouse and human kidneys. Thus, our fast and simple protocol can be beneficial for conventional microscopic evaluation of kidney tissue integrity both in research and possibly in future clinical routines., QC 20220520

In recent years, many light-microscopy protocols have been published for visualization of nanoscale structures in the kidney. These protocols present researchers with new tools to evaluate both foot process anatomy and effacement, as well as protein distributions in foot processes, the slit diaphragm and in the glomerular basement membrane. However, these protocols either involve the application of different complicated super resolution microscopes or lengthy sample preparation protocols. Here, we present a fast and simple, five-hour long procedure for three-dimensional visualization of kidney morphology on all length scales. The protocol combines optical clearing and tissue expansion concepts to produce a mild swelling, sufficient for resolving nanoscale structures using a conventional confocal microscope. We show that the protocol can be applied to visualize a wide variety of pathologic features in both mouse and human kidneys. Thus, our fast and simple protocol can be beneficial for conventional microscopic evaluation of kidney tissue integrity both in research and possibly in future clinical routines.

Cell cultures are often used to study physiological processes in health and disease. It is well-known that cells change their gene expression in vitro compared to in vivo, but it is rarely experimentally addressed. High glucose is a known trigger of apoptosis in proximal tubular cells (PTC). Here we used RNA-seq to detect differentially expressed genes in cultures of primary rat PTC, 3 days old, compared to cells retrieved directly from rat outer renal cortex and between PTC exposed to 15 mM glucose and control for 8 h. The expression of 6,174 genes was significantly up- or downregulated in the cultures of PTC compared to the cells in the outer renal cortex. Most altered were mitochondrial and metabolism related genes. Gene expression of proapoptotic proteins were upregulated and gene expression of antiapoptotic proteins were downregulated in PTC. Expression of transporter related genes were generally downregulated. After 8 h, high glucose had not altered the gene expression in PTC. The current study provides evidence that cells alter their gene expression in vitro compared to in vivo and suggests that short-term high glucose exposure can trigger apoptosis in PTC without changing the gene expression levels of apoptotic proteins., QC 20200729

Cell cultures are often used to study physiological processes in health and disease. It is well-known that cells change their gene expression in vitro compared to in vivo, but it is rarely experimentally addressed. High glucose is a known trigger of apoptosis in proximal tubular cells (PTC). Here we used RNA-seq to detect differentially expressed genes in cultures of primary rat PTC, 3 days old, compared to cells retrieved directly from rat outer renal cortex and between PTC exposed to 15 mM glucose and control for 8 h. The expression of 6,174 genes was significantly up- or downregulated in the cultures of PTC compared to the cells in the outer renal cortex. Most altered were mitochondrial and metabolism related genes. Gene expression of proapoptotic proteins were upregulated and gene expression of antiapoptotic proteins were downregulated in PTC. Expression of transporter related genes were generally downregulated. After 8 h, high glucose had not altered the gene expression in PTC. The current study provides evidence that cells alter their gene expression in vitro compared to in vivo and suggests that short-term high glucose exposure can trigger apoptosis in PTC without changing the gene expression levels of apoptotic proteins.

The ion pump Na+, K+-ATPase (NKA) is a receptor for the cardiotonic steroid ouabain. Subsaturating concentration of ouabain triggers intracellular calcium oscillations, stimulates cell proliferation and adhesion, and protects from apoptosis. However, it is controversial whether ouabain-bound NKA is considered a signal transducer. To address this question, we performed a global analysis of protein phosphorylation in COS-7 cells, identifying 2580 regulated phosphorylation events on 1242 proteins upon 10- and 20-min treatment with ouabain. Regulated phosphorylated proteins include the inositol triphosphate receptor and stromal interaction molecule, which are essential for initiating calcium oscillations. Hierarchical clustering revealed that ouabain triggers a structured phosphorylation response that occurs in a well-defined, time-dependent manner and affects specific cellular processes, including cell proliferation and cell-cell junctions. We additionally identify regulation of the phosphorylation of several calcium and calmodulin-dependent protein kinases (CAMKs), including 2 sites of CAMK type II-gamma (CAMK2G), a protein known to regulate apoptosis. To verify the significance of this result, CAMK2G was knocked down in primary kidney cells. CAMK2G knockdown impaired ouabain-dependent protection from apoptosis upon treatment with high glucose or serum deprivation. In conclusion, we establish NKA as the coordinator of a broad, tightly regulated phosphorylation response in cells and define CAMK2G as a downstream effector of NKA.-Panizza, E., Zhang, L., Fontana, J. M., Hamada, K., Svensson, D., Akkuratov, E. E., Scott, L., Mikoshiba, K., Brismar, H., Lehtio, J., Aperia, A. Ouabain-regulated phosphoproteome reveals molecular mechanisms for Na+, K+-ATPase control of cell adhesion, proliferation, and survival., QC 20190924

It is generally believed that cells that are unable to downregulate glucose transport are particularly vulnerable to hyperglycemia. Yet little is known about the relation between expression of glucose transporters and acute toxic effects of high glucose exposure.Here we have, in an ex vivo study on rat renal cells, compared the apoptotic response to a moderate increase in glucose concentration. We have studied the cell types that commonly are targeted in diabetic kidney disease (DKD): proximal tubule cells (PTC) that express SGLT2, mesangial cells (MC) that express SGLT1, and podocytes that lack SGLT and take up glucose via the insulin dependent GLUT4.PTC and MC responded within 4-8 h exposure to 15 mM glucose with translocation of the apoptotic protein Bax to mitochondria and increased apoptotic index. SGLT down-regulation and exposure to SGLT inhibitors abolished the apoptotic response. Onset of overt DKD generally coincides with onset of albuminuria. Albumin had an additive effect on the apoptotic response. Ouabain, which interferes with apoptotic onset, rescued from the apoptotic response. Insulin supplemented podocytes remained resistant to 15 and 30 mM glucose for at least 24 h.Our study points to a previously unappreciated role of SGLT dependent glucose uptake as a risk-factor for diabetic complications and highlights the importance of therapeutic approaches that specifically target the different cell types in DKD., QC 20190429

The glomerular filtration barrier, has historically only been spatially resolved using electron microscopy due to the nanometer-scale dimensions of these structures. Recently, it was shown that the nanoscale distribution of proteins in the slit diaphragm can be resolved by fluorescence based stimulated emission depletion microscopy, in combination with optical clearing. Fluorescence microscopy has advantages over electron microscopy in terms of multiplex imaging of different epitopes, and also the amount of volumetric data that can be extracted from thicker samples. However, stimulated emission depletion microscopy is still a costly technique commonly not available to most life science researchers. An imaging technique with which the glomerular filtration barrier can be visualized using more standard fluorescence imaging techniques is thus desirable. Recent studies have shown that biological tissue samples can be isotropically expanded, revealing nanoscale localizations of multiple epitopes using confocal microscopy. Here we show that kidney samples can be expanded sufficiently to study the finest elements of the filtration barrier using confocal microscopy. Thus, our result opens up the possibility to study protein distributions and foot process morphology on the effective nanometer-scale., QC 20180518

QC 20171023

Background: Blockers of angiotensin II type 1 receptor (AT 1 R) and the voltage gated calcium channel 1.2 (Ca V 1.2) are commonly used for treatment of hypertension. Yet there is little information about the effect of physiological concentrations of angiotensin II (AngII) on AT 1 R signaling and whether there is a reciprocal regulation of AT 1 R signaling by Ca V 1.2. Methods: To elucidate these questions, we have studied the Ca 2+ signaling response to physiological and pharmacological AngII doses in HEK293a cells, vascular smooth muscle cells and cardiomyocytes using a Ca 2+ sensitive dye as the principal sensor. Intra-cellular calcium recordings were performed in presence and absence of Ca V 1.2 blockers. Semi- quantitative imaging methods were used to assess the plasma membrane expression of AT 1 R and G-protein activation. Results: Repeated exposure to pharmacological (100 nM) concentrations of AngII caused, as expected, a down-regulation of the Ca 2+ response. In contrast, repeated exposure to physiological (1 nM) AngII concentration resulted in an enhancement of the Ca 2+ response. The up-regulation of the Ca 2+ response to repeated 1 nM AngII doses and the down- egulation of the Ca 2+ response to repeated 100 nM Angll doses were not accompanied by a parallel change of the AT 1 R plasma membrane expression. The Ca 2+ response to 1 nM of AngII was amplified in the presence of therapeutic concentrations of the Ca V 1.2 blockers, nifedipine and verapamil, in vascular smooth muscle cells, cardiomyocytes and HEK293a cells. Amplification of the AT 1 R response was also observed following inhibition of the calcium permeable transient receptor potential cation channels, suggesting that the activity of AT 1 R is sensitive to calcium influx. Conclusions: Our findings have implications for the understanding of hyperactivity of the angiotensin system and for use of Ca 2+ channel blockers as mono-therapy in hypertension., QC 20170328

There is a great need for treatment that arrests progression of chronic kidney disease. Increased albumin in urine leads to apoptosis and fibrosis of podocytes and tubular cells and is a major cause of functional deterioration. There have been many attempts to target fibrosis, but because of the lack of appropriate agents, few have targeted apoptosis. Our group has described an ouabain-activated Na,K-ATPase/IP3R signalosome, which protects from apoptosis. Here we show that albumin uptake in primary rat renal epithelial cells is accompanied by a time-and dose-dependent mitochondrial accumulation of the apoptotic factor Bax, down-regulation of the antiapoptotic factor Bcl-xL and mitochondrial membrane depolarization. Ouabain opposes these effects and protects from apoptosis in albumin-exposed proximal tubule cells and podocytes. The efficacy of ouabain as an antiapoptotic and kidney-protective therapeutic tool was then tested in rats with passive Heymann nephritis, a model of proteinuric chronic kidney disease. Chronic ouabain treatment preserved renal function, protected from renal cortical apoptosis, up-regulated Bax, down-regulated Bcl-xL, and rescued from glomerular tubular disconnection and podocyte loss. Thus we have identified a novel clinically feasible therapeutic tool, which has the potential to protect from apoptosis and rescue from loss of functional tissue in chronic proteinuric kidney disease., QC 20160715

The glomerular filtration barrier, consisting of podocyte foot processes with bridging slit diaphragm, glomerular basement membrane, and endothelium, is a key component for renal function. Previously, the subtlest elements of the filtration barrier have only been visualized using electron microscopy. However, electron microscopy is mostly restricted to ultrathin two-dimensional samples, and the possibility to simultaneously visualize multiple different proteins is limited. Therefore, we sought to implement a super-resolution immunofluorescence microscopy protocol for the study of the filtration barrier in the kidney. Recently, several optical clearing methods have been developed making it possible to image through large volumes of tissue and even whole organs using light microscopy. Here we found that hydrogel-based optical clearing is a beneficial tool to study intact renal tissue at the nanometer scale. When imaging samples using super-resolution STED microscopy, the staining quality was critical in order to assess correct nanoscale information. The signal-to-noise ratio and immunosignal homogeneity were both improved in optically cleared tissue. Thus, STED of slit diaphragms in fluorescently labelled optically cleared intact kidney samples is a new tool for studying the glomerular filtration barrier in health and disease., QC 20160218

QC 20151105

QC 20151102

QC 20131211

Postsynaptic receptor trafficking plays an essential role in tuning neurotransmission and signal plasticity and has emerged as a potential therapeutic target in neuropsychiatric disease. Using a novel application of fluorescence recovery after photobleaching in rat hippocampal neurons, we examined transport from the soma to dendrites of seven G-protein-coupled receptors (GPCRs) implicated in mood disorders. Most GPCRs were delivered to dendrites via lateral diffusion, but one GPCR, the serotonin 1B receptor (5-HT1B), was delivered to the dendrites in secretory vesicles. Within the dendrites, 5-HT1B were stored in a reservoir of accessible vesicles that were recruited to preferential sites in plasma membrane, as observed with superecliptic pHluorin labeling. After membrane recruitment, 5-HT1B transport via lateral diffusion and temporal confinement to inhibitory and excitatory synapses was monitored by single particle tracking. These results suggest an alternative mechanism for control of neuronal activity via a GPCR that has been implicated in mood regulation., QC 20130110

Protein localization in dendritic spines is the focus of intense investigations within neuroscience. Applications of super-resolution microscopy to dissect nanoscale protein distributions, as shown in this work with dual-color STED, generate spatial correlation coefficients having quite small values. This means that colocalization analysis to some extent looses part of its correlative impact. In this study we thus introduced nearest neighbor analysis to quantify the spatial relations between two important proteins in neurons, the dopamine D1 receptor and Na+,K+-ATPase. The analysis gave new information on how dense the D1 receptor and Na+,K+-ATPase constituting nanoclusters are located both with respect to the homogenous (self to same) and the heterogeneous (same to other) topology. The STED dissected nanoscale topologies provide evidence for both a joint as well as a separated confinement of the D1 receptor and the Na+,K+-ATPase in the postsynaptic areas of dendritic spines. This confined topology may have implications for generation of local sodium gradients and for structural and functional interactions modulating slow synaptic transmission processes. Microsc. Res. Tech., 2011., QC 20120309

Background: The Na+,K+-ATPase plays an important role for ion homeostasis in virtually all mammalian cells, including neurons. Despite this, there is as yet little known about the isoform specific distribution in neurons. Results: With help of superresolving stimulated emission depletion microscopy the spatial distribution of Na+,K+-ATPase in dendritic spines of cultured striatum neurons have been dissected. The found compartmentalized distribution provides a strong evidence for the confinement of neuronal Na+,K+-ATPase (alpha 3 isoform) in the postsynaptic region of the spine. Conclusions: A compartmentalized distribution may have implications for the generation of local sodium gradients within the spine and for the structural and functional interaction between the sodium pump and other synaptic proteins. Superresolution microscopy has thus opened up a new perspective to elucidate the nature of the physiological function, regulation and signaling role of Na+,K+-ATPase from its topological distribution in dendritic spines., QC 20110307

Background: The Na+,K+-ATPase plays an important role for ion homeostasis in virtually all mammalian cells, including neurons. Despite this, there is as yet little known about the isoform specific distribution in neurons. Results: With help of superresolving stimulated emission depletion microscopy the spatial distribution of Na+,K+-ATPase in dendritic spines of cultured striatum neurons have been dissected. The found compartmentalized distribution provides a strong evidence for the confinement of neuronal Na+,K+-ATPase (alpha 3 isoform) in the postsynaptic region of the spine. Conclusions: A compartmentalized distribution may have implications for the generation of local sodium gradients within the spine and for the structural and functional interaction between the sodium pump and other synaptic proteins. Superresolution microscopy has thus opened up a new perspective to elucidate the nature of the physiological function, regulation and signaling role of Na+,K+-ATPase from its topological distribution in dendritic spines., QC 20110307

Background: The Na+,K+-ATPase plays an important role for ion homeostasis in virtually all mammalian cells, including neurons. Despite this, there is as yet little known about the isoform specific distribution in neurons. Results: With help of superresolving stimulated emission depletion microscopy the spatial distribution of Na+,K+-ATPase in dendritic spines of cultured striatum neurons have been dissected. The found compartmentalized distribution provides a strong evidence for the confinement of neuronal Na+,K+-ATPase (alpha 3 isoform) in the postsynaptic region of the spine. Conclusions: A compartmentalized distribution may have implications for the generation of local sodium gradients within the spine and for the structural and functional interaction between the sodium pump and other synaptic proteins. Superresolution microscopy has thus opened up a new perspective to elucidate the nature of the physiological function, regulation and signaling role of Na+,K+-ATPase from its topological distribution in dendritic spines., QC 20110307

Background: The Na+,K+-ATPase plays an important role for ion homeostasis in virtually all mammalian cells, including neurons. Despite this, there is as yet little known about the isoform specific distribution in neurons. Results: With help of superresolving stimulated emission depletion microscopy the spatial distribution of Na+,K+-ATPase in dendritic spines of cultured striatum neurons have been dissected. The found compartmentalized distribution provides a strong evidence for the confinement of neuronal Na+,K+-ATPase (alpha 3 isoform) in the postsynaptic region of the spine. Conclusions: A compartmentalized distribution may have implications for the generation of local sodium gradients within the spine and for the structural and functional interaction between the sodium pump and other synaptic proteins. Superresolution microscopy has thus opened up a new perspective to elucidate the nature of the physiological function, regulation and signaling role of Na+,K+-ATPase from its topological distribution in dendritic spines., QC 20110307

Background: The Na+,K+-ATPase plays an important role for ion homeostasis in virtually all mammalian cells, including neurons. Despite this, there is as yet little known about the isoform specific distribution in neurons. Results: With help of superresolving stimulated emission depletion microscopy the spatial distribution of Na+,K+-ATPase in dendritic spines of cultured striatum neurons have been dissected. The found compartmentalized distribution provides a strong evidence for the confinement of neuronal Na+,K+-ATPase (alpha 3 isoform) in the postsynaptic region of the spine. Conclusions: A compartmentalized distribution may have implications for the generation of local sodium gradients within the spine and for the structural and functional interaction between the sodium pump and other synaptic proteins. Superresolution microscopy has thus opened up a new perspective to elucidate the nature of the physiological function, regulation and signaling role of Na+,K+-ATPase from its topological distribution in dendritic spines., QC 20110307

Calcyon is a brain-specific protein, implicated in clathrin-mediated endocytosis. In this descriptive study we show that calcyon is exclusively expressed in neurons, and localized in moving vesicles. The movement of calcyon-containing vesicles was dependent on temperature and on intact microtubules, in addition these vesicles were colocalized with a marker for endocytosed plasma membrane proteins, suggesting that calcyon vesicles follow the endocytic recycling pathway. We also show using evanescent wave microscopy that there is a pool of ready releasable calcyon vesiclesaccumulated beneath the plasma membrane. We conclude that the mobility and storage properties of calcyon-containing vesicles imply that they play a role in brain plasticity., QC 20100525

The dopaminergic and glutamatergic systems interact to initiate and organize normal behavior, a communication that may be perturbed in many neuropsychiatric diseases, including schizophrenia. We show here that NMDA, by allosterically modifying NMDA receptors, can act as a scaffold to recruit laterally diffusing dopamine D1 receptors (D1R) to neuronal spines. Using organotypic culture from rat striatum transfected with D1R fused to a fluorescent protein, we show that the majority of dendritic D1R are in lateral diffusion and that their mobility is confined by interaction with NMDA receptors. Exposure to NMDA reduces the diffusion coefficient for D1R and causes an increase in the number of D1R-positive spines. Unexpectedly, the action of NMDA in potentiating D1R recruitment was independent of calcium flow via the NMDA receptor channel. Thus, a highly energy-efficient, diffusion-trap mechanism can account for intraneuronal interaction between the glutamatergic and dopaminergic systems and for regulation of the number of D1R-positive spines. This diffusion trap system represents a molecular mechanism for brain plasticity and offers a promising target for development of antipsychotic therapy, QC 20100726

NQC

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Dopamine is a key neurotransmitter in the brain, and has an important modulatory role in the control of motor activity and cognitive processes. Dysfunctions of the dopamine system have been implicated in several neuropsychiatric disorders such as schizophrenia and attention-deficit/hyperactivity disorder. In this thesis we address questions concerning plasticity of the dopamine DI receptor system by performing both behavioral studies, looking at potential postnatal maturational changes in D1 receptor mediated motor activity, and in vitro studies, looking at potential effects of NMDA receptor activation on dopamine signaling. We show that DI receptor activation can induce both inhibition and stimulation of motor activity, and that the development of these two response patterns are different, and associated with distinct patterns of c-fos expression within the prefrontal cortex and striatum. We also show that functional DARPP-32 signaling is necessary for the development of the motor stimulatory effects of D1 receptors. There is increasing evidence indicating that interactions between different types of neurotransmitter receptors represent a major mechanism of neuronal plasticity. To explore the molecular mechanisms behind dopamine plasticity, we have performed a series of experimental studies on primary cell cultures and organotypic cultures. We have shown that NMDA receptor activation induces DI receptor recruitment to dendritic spines and that this recruitment is dependent on interaction between the D1 receptor and the NMDA receptor. We demonstrate that there is a reservoir pool of DI receptors diffusing in dendrites and that these receptors can, following NMDA receptor activation, be trapped by interaction with NMDA receptors. We have shown with behavior studies a series of manifestations of plasticity in dopamine signaling, and provided evidence for a regulated recruitment of a G-protein coupled receptor to functional sites in neurons, and provided a basis for th

Real-time PCR was evaluated as a quantitative diagnostic method for Chlamydia pneumoniae infection using different respiratory samples. Real-time PCR had efficiency equal to or better than that of nested touchdown PCR. This study confirmed sputum as the best sampling material to detect an ongoing C. pneumoniae infection.

QC 20190404

QC 20190428

QC 20190428

The subtlest element of the kidney, such as the slit diaphragm, has historically only been spatially resolved using electron microscopy due to the nanometer-scale dimensions of these structures. Recently, it was shown that the nanoscale distribution of proteins in the slit diaphragm can be resolved by fluorescence based stimulated emission depletion (STED) microscopy, in combination with optical clearing. Fluorescence microscopy has advantages over electron microscopy in terms of multiplex imaging of different molecular species (i.e. epitopes), and also the amount of volumetric data that can be extracted from a thick sample. However, STED microscopy is still a costly technique commonly not available to all life science researchers. An image technique with which the slit diaphragm proteins in the kidney can be visualized using more standard fluorescence imaging techniques is thus desirable. Recent studies have shown that biological tissue samples can be isotropically expanded while optically cleared, revealing nanoscale localizations of multiple epitopes using confocal microscopy. Here we show that kidney samples can be expanded sufficiently to study the finest elements of the filtration barrier under both healthy and diseased conditions using confocal microscopy. This finding opens up the possibility for any researcher with access to a confocal microscope to study foot process protein distributions on the effective nanometer-scale. We also show that expansion microscopy can be combined with STED microscopy to further increase the effective spatial resolution down to below 20 nm., QC 20170523

The role of the Bcl-family proteins in the mitochondrial apoptotic process is well described with biochemical and molecular methods in studies of isolated mitochondria and transfected cell lines. There is however little knowledge about the mechanisms for Bcl protein interaction leading to apoptosis in intact cells. In particular, the time sequence and location for Bcl protein interaction has so far only been described in hypothetical models.Here we have used Stimulated Emission Depletion (STED) microscopy and Single Molecule Localization Microscopy (SMLM) to study the apoptotic process in immune-stained rat renal epithelia cells exposed to 20 mM glucose (HG) and to study its rescue by ouabain. To assess distance between Bcl-2 proteins, we used the nearest-neighbor algorithm. The anti-apoptotic protein Bcl-xLl was predominantly expressed on mitochondria in control cells, and remained so throughout the process, although its abundance decreased. After 2h HG the apoptosis-inducing protein BAD had translocated from the cytoplasm to the mitochondria where it clustered with Bcl-xL. This occurred before an increase in reactive oxygen species and was dependent on activation of the PI3K –AKT pathway. According to current concepts, Bcl-xL interacts with the apoptotic protein Bax on the mitochondria under control conditions to translocate Bax back to the cytosol1. We found that Bax started to accumulate on the mitochondria after 4h HG and, surprisingly, that the interaction between Bcl-xL and Bax became more pronounced during the course of the apoptotic process. After 6h HG Bax also interacted with the non-specific ion transporter VDAC; an interaction described to lead to penetration of the inner mitochondrial membrane and mark the point of no return., QC 20171003