17 results on '"Rescher, Ursula"'
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2. Annexin A8 promotes VEGF-A driven endothelial cell sprouting
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Heitzig, Nicole, Brinkmann, Benjamin F., Koerdt, Sophia N., Rosso, Gonzalo, Shahin, Victor, and Rescher, Ursula
- Abstract
ABSTRACTThe physiological and pathological process of angiogenesis relies on orchestrated endothelial cell (EC) adhesion, migration and formation of new vessels. Here we report that human umbilical vein endothelial cells (HUVECs) deficient in Annexin A8 (AnxA8), a member of the annexin family of Ca2+- and membrane binding proteins, are strongly deficient in their ability to sprout in response to vascular endothelial growth factor (VEGF)-A, and are strongly impaired in their ability to migrate and adhere to β1 integrin-binding extracellular matrix (ECM) proteins. We find that these cells are defective in the formation of complexes containing the tetraspanin CD63, the main VEGF-A receptor VEGFR2, and the β1 integrin subunit, on the cell surface. We observe that upon VEGF-A activation of AnxA8-depleted HUVECs, VEGFR2 internalization is reduced, phosphorylation of VEGFR2 is increased, and the spatial distribution of Tyr577-phosphorylated focal adhesion kinase (pFAK577) is altered. We conclude that AnxA8 affects CD63/VEGFR2/β1 integrin complex formation, leading to hyperactivation of the VEGF-A signal transduction pathway, and severely disturbed VEGF-A-driven angiogenic sprouting.
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- 2017
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3. P-selectin-dependent leukocyte adhesion is governed by endolysosomal two-pore channel 2
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Goretzko, Jonas, Pauels, Inga, Heitzig, Nicole, Thomas, Katharina, Kardell, Marina, Naß, Johannes, Krogsaeter, Einar Kleinhans, Schloer, Sebastian, Spix, Barbara, Linard Matos, Anna Lívia, Leser, Charlotte, Wegner, Tristan, Glorius, Frank, Bracher, Franz, Gerke, Volker, Rossaint, Jan, Grimm, Christian, and Rescher, Ursula
- Abstract
Upon proinflammatory challenges, endothelial cell surface presentation of the leukocyte receptor P-selectin, together with the stabilizing co-factor CD63, is needed for leukocyte capture and is mediated via demand-driven exocytosis from the Weibel-Palade bodies that fuse with the plasma membrane. We report that neutrophil recruitment to activated endothelium is significantly reduced in mice deficient for the endolysosomal cation channel TPC2 and in human primary endothelial cells with pharmacological TPC2 block. We observe less CD63 signal in whole-mount stainings of proinflammatory-activated cremaster muscles from TPC2 knockout mice. We find that TPC2 is activated and needed to ensure the transfer of CD63 from endolysosomes via Weibel-Palade bodies to the plasma membrane to retain P-selectin on the cell surface of human primary endothelial cells. Our findings establish TPC2 as a key element to leukocyte interaction with the endothelium and a potential pharmacological target in the control of inflammatory leukocyte recruitment.
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- 2023
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4. Can you teach an old receptor new tricks?
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Raabe, Carsten Alexander and Rescher, Ursula
- Abstract
. Discussion on biased agonism of the human formyl peptide receptor 1 (FPR1) for precision therapeutic targeting of neutrophil function.
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- 2021
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5. Annexin A8 Regulates Late Endosome Organization and Function
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Goebeler, Verena, Poeter, Michaela, Zeuschner, Dagmar, Gerke, Volker, and Rescher, Ursula
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Different classes of endosomes exhibit a characteristic intracellular steady-state distribution governed by interactions with the cytoskeleton. Late endosomes, organelles of the degradative lysosomal route, seem to require associated actin filaments for proper localization and function. We show here that the F-actin and phospholipid binding protein annexin A8 is associated specifically with late endosomes. Altering intracellular annexin A8 levels drastically affected the morphology and intracellular distribution of late endosomes. Trafficking through the degradative pathway was delayed in the absence of annexin A8, resulting in attenuated ligand-induced degradation of the epidermal growth factor receptor and prolonged epidermal growth factor-induced activation of mitogen-activated protein kinase. Depletion of annexin A8 reduced the association of late endosomal membranes with actin filaments. These results indicate that the defective cargo transport through the late endocytic pathway and the imbalanced signaling of activated receptors observed in the absence of annexin A8 results from the disturbed association of late endosomal membranes with the actin network, resulting in impaired actin-based late endosome motility.
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- 2008
6. Annexin A8 Regulates Late Endosome Organization and Function
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Goebeler, Verena, Poeter, Michaela, Zeuschner, Dagmar, Gerke, Volker, and Rescher, Ursula
- Abstract
Different classes of endosomes exhibit a characteristic intracellular steady-state distribution governed by interactions with the cytoskeleton. Late endosomes, organelles of the degradative lysosomal route, seem to require associated actin filaments for proper localization and function. We show here that the F-actin and phospholipid binding protein annexin A8 is associated specifically with late endosomes. Altering intracellular annexin A8 levels drastically affected the morphology and intracellular distribution of late endosomes. Trafficking through the degradative pathway was delayed in the absence of annexin A8, resulting in attenuated ligand-induced degradation of the epidermal growth factor receptor and prolonged epidermal growth factor-induced activation of mitogen-activated protein kinase. Depletion of annexin A8 reduced the association of late endosomal membranes with actin filaments. These results indicate that the defective cargo transport through the late endocytic pathway and the imbalanced signaling of activated receptors observed in the absence of annexin A8 results from the disturbed association of late endosomal membranes with the actin network, resulting in impaired actin-based late endosome motility.
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- 2008
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7. Transcriptional profiling of human monocytes reveals complex changes in the expression pattern of inflammation‐related genes in response to the annexin A1‐derived peptide Ac1‐25
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Lange, Carsten, Starrett, Diane J., Goetsch, Julia, Gerke, Volker, and Rescher, Ursula
- Abstract
Annexin A1 is a glucocorticoid‐regulated, anti‐inflammatory protein, which plays an important role as an endogenous regulator of the inflammatory response. Many of these anti‐inflammatory properties are retained in the N‐terminal annexin A1 peptide Ac1‐25, which is released from the full‐length protein by a neutrophil elastase. To elucidate whether the anti‐inflammatory activity of the bioactive peptide is solely a result of immediate post‐translational effects, which include the shedding of L‐selectin or also involve transcriptional changes affecting leukocyte function, we recorded global gene expression changes in human monocytes stimulated with exogenously applied Ac1‐25. Applying stringent selection criteria, we show that ∼100 genes are up‐regulated, and ∼230 are down‐regulated by a factor of at least two in the Ac1‐25‐treated monocytes. It is important that the profiling reveals that Ac1‐25 induces an anti‐inflammatory phenotype by down‐regulating proinflammatory and up‐regulating anti‐inflammatory mediators. These effects, elicited by exogenously applied Ac1‐25, depend, to different extents, on ERK1/2 and p38 signaling pathways. This identifies the annexin A1 N‐terminal peptide as a stimulus, eliciting not only short‐term, post‐translational effects in human monocytes but also transcriptional changes, defining a more anti‐inflammatory profile.
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- 2007
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8. The Annexin 2/S100A10 Complex Controls the Distribution of Transferrin Receptor-containing Recycling Endosomes
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Zobiack, Nicole, Rescher, Ursula, Ludwig, Carsten, Zeuschner, Dagmar, and Gerke, Volker
- Abstract
The Ca2+- and lipid-binding protein annexin 2, which resides in a tight heterotetrameric complex with the S100 protein S100A10 (p11), has been implicated in the structural organization and dynamics of endosomal membranes. To elucidate the function of annexin 2 and S100A10 in endosome organization and trafficking, we used RNA-mediated interference to specifically suppress annexin 2 and S100A10 expression. Down-regulation of both proteins perturbed the distribution of transferrin receptor- and rab11-positive recycling endosomes but did not affect uptake into sorting endosomes. The phenotype was highly specific and could be rescued by reexpression of the N-terminal annexin 2 domain or S100A10 in annexin 2- or S100A10-depleted cells, respectively. Whole-mount immunoelectron microscopy of the aberrantly localized recycling endosomes in annexin 2/S100A10 down-regulated cells revealed extensively bent tubules and an increased number of endosome-associated clathrin-positive buds. Despite these morphological alterations, the kinetics of transferrin uptake and recycling was not affected to a significant extent, indicating that the proper positioning of recycling endosomes is not a rate-limiting step in transferrin recycling. The phenotype generated by this transient loss-of-protein approach shows for the first time that the annexin 2/S100A10 complex functions in the intracellular positioning of recycling endosomes and that both subunits are required for this activity.
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- 2003
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9. Cell-surface attachment of pedestal-forming enteropathogenic E. coli induces a clustering of raft components and a recruitment of annexin 2
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Zobiack, Nicole, Rescher, Ursula, Laarmann, Sven, Michgehl, Silke, Schmidt, M. Alexander, and Gerke, Volker
- Abstract
Annexin 2 is a Ca2+-regulated membrane- and F-actin-binding protein implicated in the stabilization or regulation of membrane/cytoskeleton contacts, or both, at the plasma membrane and at early endosomal membranes. To analyze the dynamic nature of such action we investigated whether annexin 2 could be found at sites of localized actin rearrangements occurring at the plasma membrane of HeLa cells infected with noninvading enteropathogenic Escherichia coli (EPEC). We show that adherent EPEC microcolonies, which are known to induce the formation of actin-rich pedestals beneath them, specifically recruit annexin 2 to the sites of their attachment. Mutant EPEC (EPECtir), which lack a functional receptor for intimate attachment (Tir, translocated intimin receptor) and which fail to produce full pedestal formation, are still capable of recruiting annexin 2 to the bacterial contact sites. Accumulation of annexin 2 at sites of EPEC or EPECtir attachment is accompanied by a recruitment of the annexin 2 protein ligand S100A10. EPEC and EPECtir attachment also induces a concentration of cholesterol and glycosyl phosphatidylinositol-anchored proteins at sites of bacterial contact. This indicates that membrane components present in rafts or raft-like microdomains are clustered upon EPEC adherence and that annexin 2 is recruited to the cytoplasmic membrane surface of such clusters, possibly stabilizing raft patches and their linkage to the actin cytoskeleton beneath adhering EPEC.
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- 2002
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10. Complex formation and submembranous localization of annexin 2 and S100A10 in live HepG2 cells
- Author
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Zobiack, Nicole, Gerke, Volker, and Rescher, Ursula
- Abstract
The Ca2+and membrane binding protein annexin 2 can form a heterotetrameric complex with the S100A10 protein and this complex is thought to serve a bridging or scaffolding function in the membrane underlying cytoskeleton. To elucidate which of the subunits targets the complex to the subplasmalemmal region in live cells we employed YFP/CFP fusion proteins and live cell imaging in HepG2 cells. We show that monomeric annexin 2 is targeted to the plasma membrane whereas non‐complexed S100A10 acquires a general cytosolic distribution. Co‐expression of S100A10 together with annexin 2 and the resulting complex formation, however, lead to a recruitment of S100A10 to the plasma membrane thus identifying annexin 2 as the membrane targeting subunit.
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- 2001
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11. Complex formation and submembranous localization of annexin 2 and S100A10 in live HepG2 cells
- Author
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Zobiack, Nicole, Gerke, Volker, and Rescher, Ursula
- Abstract
The Ca 2+and membrane binding protein annexin 2 can form a heterotetrameric complex with the S100A10 protein and this complex is thought to serve a bridging or scaffolding function in the membrane underlying cytoskeleton. To elucidate which of the subunits targets the complex to the subplasmalemmal region in live cells we employed YFP/CFP fusion proteins and live cell imaging in HepG2 cells. We show that monomeric annexin 2 is targeted to the plasma membrane whereas non-complexed S100A10 acquires a general cytosolic distribution. Co-expression of S100A10 together with annexin 2 and the resulting complex formation, however, lead to a recruitment of S100A10 to the plasma membrane thus identifying annexin 2 as the membrane targeting subunit.
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- 2001
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12. Intact Ca2+-binding sites are required for targeting of annexin 1 to endosomal membranes in living HeLa cells
- Author
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Rescher, Ursula, Zobiack, Nicole, and Gerke, Volker
- Abstract
Annexin 1 is a Ca2+-regulated membrane binding protein and a major substrate of the epidermal growth factor receptor kinase. Because of its properties and intracellular distribution, the protein has been implicated in endocytic trafficking of the receptor, in particular in receptor sorting occurring in multivesicular endosomes. Up to now, however, the localization of annexin 1 to cellular membranes has been limited to subcellular fractionation and immunocytochemical analyses of fixed cells. To establish its localization in live cells, we followed the intracellular fate of annexin 1 molecules fused to the Green Fluorescent Protein (GFP). We show that annexin 1-GFP associates with distinct, transferrin receptor-positive membrane structures in living HeLa cells. A GFP chimera containing the Ca2+/phospholipid-binding protein core of annexin 1 also shows a punctate intracellular distribution, although the structures labeled here do not resemble early but, at least in part, late endosomes. In contrast, the cores of annexins 2 and 4 fused to GFP exhibit a cytoplasmic or a different punctate distribution, respectively, indicating that the highly homologous annexin core domains carry distinct membrane specificities within live cells. By inactivating the three high-affinity Ca2+ binding sites in annexin 1 we also show that endosomal membrane binding of the protein in live HeLa cells depends on the integrity of these Ca2+ binding sites. More detailed analysis identifies a single Ca2+ site in the second annexin repeat that is crucially involved in establishing the membrane association. These results reveal for the first time that intracellular membrane binding of an annexin in living cells requires Ca2+ and is mediated in part through an annexin core domain that is capable of establishing specific interactions.
- Published
- 2000
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13. Ineffective Elimination of LeishmaniaMajor by Inflammatory (MRP 14-Positive) Subtype of Monocytic Cells
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Steinbrink, Kerstin, SchÖnlau, Frank, Rescher, Ursula, Henseleit, Ute, Vogel, Thomas, Sorg, Clemens, and Sunderötter, Cord
- Abstract
Myeloid-related protein (MRP) 14, an intracellular protein involved in calcium-dependent activation of myeloid cells, presents a differentiation marker for a subtype of macrophages. In experimental leishmaniasis, BALB/c mice succumb to visceral dissemination after infection with L. major, due to a Th2 cell response, while C57Bl/6 mice develop protective immunity associated with a Thl cell response. We have previously shown that resistance in C57Bl/6 mice was also associated with a significantly lower percentage of MRP14-positive cells in the infiltrate than in susceptible BALB/c mice. In C57Bl/6 mice, weekly injections of bone marrow (BM) cells enriched with MRP14-positive cells (dl of culture) did not reverse, but prolonged the course of infection, associated with increased local parasite spread. In BALB/c mice a single dose of an antiphlogistic agent (dexamethasone or lipoxygenase inhibitor) was associated with reduction of infiltrating MRP14-positive cells and also with a decrease of parasite loads in footpads, lymph nodes as well as spleens, and with delayed progression of disease.
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- 2000
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14. Antibodies against distinct ABP1 regions modify auxin binding to ABP1 and change the physiological auxin response of maize coleoptile cections
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Walther, Antje, Rescher, Ursula, Schiebl, Christine, and Klämbt, Dieter
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Twelve peptides spanning the whole maize ABP1 sequence were synthesized and coupled to sepharose. Peptide — specific antibodies were purified from and ABP1 IgGs on peptide affinity columns, and binding of NAA to purified ABP1 in the presence of the IgGs was assayed. Of all the antibodies tested, only three increased the KDof auxin binding. Correspondingly, auxin-caused pH shift of the incubation medium by coleoptile sections was strongly influenced by these three antibodies. In addition, antibodies directed against the peptides corresponding to the N- and the C-terminus were also able to reduce the auxin-induced pH drop.
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- 1997
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15. Interaction of auxin-binding protein 1 with maize coleoptile plasma membranes in vitro
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Schiebl, Christine, Walther, Antje, Rescher, Ursula, and Klämbt, Dieter
- Abstract
Abstract.: In a search for membrane “docking proteins” interacting with Zea mays auxin-binding protein (ABP1) the binding of purified ABP1 to maize coleoptile plasma-membrane vesicles was investigated. Concentration-dependent, saturable binding of ABP1 to the membrane vesicles was observed in binding assays using 10
−8 –10−6 ␣M ABP1. Biotinylated ABP1 was displaced from the membrane binding sites by competition with unlabeled ABP1, demonstrating specific binding. The association step proved to be pH-dependent with maximum binding at pH 5.0 or lower. Auxins did not influence the ABP1 binding to plasma-membrane vesicles, but ABP1 associated with plasma-membrane vesicles was still able to specifically bind [3 H]naphthalene-1-acetic acid. The rather stable interaction of ABP1 with plasma-membrane vesicles was only affected by strong alkaline buffers or detergents. The binding capacity was calculated to be in the range of 0.2 pmol ABP1 per g coleoptile fresh weight.- Published
- 1997
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16. Late Endosomal/Lysosomal Cholesterol Accumulation Is a Host Cell-Protective Mechanism Inhibiting Endosomal Escape of Influenza A Virus
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Kühnl, Alexander, Musiol, Agnes, Heitzig, Nicole, Johnson, Danielle E., Ehrhardt, Christina, Grewal, Thomas, Gerke, Volker, Ludwig, Stephan, and Rescher, Ursula
- Abstract
ABSTRACTTo transfer the viral genome into the host cell cytoplasm, internalized influenza A virus (IAV) particles depend on the fusion of the IAV envelope with host endosomal membranes. The antiviral host interferon (IFN) response includes the upregulation of interferon-induced transmembrane protein 3 (IFITM3), which inhibits the release of the viral content into the cytosol. Although IFITM3 induction occurs concomitantly with late endosomal/lysosomal (LE/L) cholesterol accumulation, the functional significance of this process is not well understood. Here we report that LE/L cholesterol accumulation itself plays a pivotal role in the early antiviral defense. We demonstrate that inducing LE/L cholesterol accumulation is antiviral in non-IFN-primed cells, restricting incoming IAV particles and impairing mixing of IAV/endosomal membrane lipids. Our results establish a protective function of LE/L cholesterol accumulation and suggest endosomal cholesterol balance as a possible antiviral target.IMPORTANCEWith annual epidemics occurring in all parts of the world and the risk of global outbreaks, influenza A virus (IAV) infections remain a major threat to public health. Infected host cells detect viral components and mount an interferon (IFN)-mediated response to restrict virus propagation and spread of infection. Identification of cellular factors and underlying mechanisms that establish such an antiviral state can provide novel strategies for the development of antiviral drugs. The contribution of LE/L cholesterol levels, especially in the context of the IFN-induced antiviral response, has remained controversial so far. Here, we report that accumulation of cholesterol in the LE/L compartment contributes to the IFN-induced host cell defense against incoming IAV. Our results establish cholesterol accumulation in LE/L per seas a novel antiviral barrier and suggest the endosomal cholesterol balance as a putative druggable host cell factor in IAV infection.
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- 2018
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17. Annexin A6-Balanced Late Endosomal Cholesterol Controls Influenza A Replication and Propagation
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Musiol, Agnes, Gran, Sandra, Ehrhardt, Christina, Ludwig, Stephan, Grewal, Thomas, Gerke, Volker, and Rescher, Ursula
- Abstract
ABSTRACTInfluenza is caused by influenza A virus (IAV), an enveloped, negative-stranded RNA virus that derives its envelope lipids from the host cell plasma membrane. Here, we examined the functional role of cellular cholesterol in the IAV infection cycle. We show that shifting of cellular cholesterol pools via the Ca2+-regulated membrane-binding protein annexin A6 (AnxA6) affects the infectivity of progeny virus particles. Elevated levels of cellular AnxA6, which decrease plasma membrane and increase late endosomal cholesterol levels, impaired IAV replication and propagation, whereas RNA interference-mediated AnxA6 ablation increased viral progeny titers. Pharmacological accumulation of late endosomal cholesterol also diminished IAV virus propagation. Decreased IAV replication caused by upregulated AnxA6 expression could be restored either by exogenous replenishment of host cell cholesterol or by ectopic expression of the late endosomal cholesterol transporter Niemann-Pick C1 (NPC1). Virus released from AnxA6-overexpressing cells displayed significantly reduced cholesterol levels. Our results show that IAV replication depends on maintenance of the cellular cholesterol balance and identify AnxA6 as a critical factor in linking IAV to cellular cholesterol homeostasis.IMPORTANCEInfluenza A virus (IAV) is a major public health concern, and yet, major host-pathogen interactions regulating IAV replication still remain poorly understood. It is known that host cell cholesterol is a critical factor in the influenza virus life cycle. The viral envelope is derived from the host cell membrane during the process of budding and, hence, equips the virus with a special lipid-protein mixture which is high in cholesterol. However, the influence of host cell cholesterol homeostasis on IAV infection is largely unknown. We show that IAV infection success critically depends on host cell cholesterol distribution. Cholesterol sequestration in the endosomal compartment impairs progeny titer and infectivity and is associated with reduced cholesterol content in the viral envelope.
- Published
- 2013
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