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This research focuses on macrofungi in Baotianman Biosphere Reserve and their relationships with plant ecosystems. The findings demonstrate the reserve’s macrofungal resources. The study collected 832 specimens, among which 351 macrofungi species were identified, belonging to six classes, 19 orders, 54 familiae, and 124 genera, and one new species of Abortiporus was found. Among them, 11 familiae with a total of 231 species were dominated, accounting for 20.37% of the total number of familiae and 65.81% of the total number of species; 14 genera with a total of 147 species were dominated, accounting for about 11.38% the total number of genera and 41.88% of the total number of species. The richness of macrofungi at the species level was considerably different across the four vegetation types in the reserve, showing that the vegetation types had a bigger influence on macrofungi. In the evaluation of macrofungal resources, a total of 196 species of edible fungi, 121 species of medicinal fungi, 52 species of poisonous fungi, and 37 species of macrofungi with unclear economic value were counted. Abortiporus baotianmanensis is a new species of podoscyphaceae in the genus Abortiporus. The new species display the reserve’s richness. Next, the project seeks to generate and conserve macrofungal resources.

Background and Purpose: Refractory wounds are a severe complication of diabetes mellitus with limited treatment regimens. Rho-associated protein kinase-1 (ROCK1) phosphorylates a series of substrates that trigger downstream signaling pathways, affecting multiple cellular processes. The present study investigated the role of ROCK1 in diabetic wound healing and molecular mechanisms. Experimental Approach: Streptozotocin (STZ)-induced diabetic mice with full-thickness excisional wound model and human umbilical vein endothelial cells (HUVECs) were used. Key Results: ROCK1 expression significantly increased in wound granulation tissues in both diabetic patients and diabetic mice. Wound healing and blood perfusion were dose-dependently improved by the ROCK1 inhibitor fasudil in diabetic mice. In endothelial cells, fasudil and ROCK1 siRNA significantly elevated the phosphorylation of adenosine monophosphate-activated protein kinase at Thr172 (pThr172-AMPKα), the activity of endothelial nitric oxide synthase (eNOS), and suppressed the levels of mitochondrial reactive oxygen species and nitrotyrosine formation. Experiments using integrated bioinformatics analysis and coimmunoprecipitation established that ROCK1 inhibited pThr172-AMPKα by binding to receptor-interacting serine/threonine kinase 4 (RIPK4). Conclusion and Implications: Fasudil accelerated wound repair and improved angiogenesis at least partially through the ROCK1/RIPK4/AMPK pathway. Fasudil may be a potential treatment for refractory wounds in diabetic patients.

Superwetting materials show distinct advantages in interfacial applications such as oil-water separation. However, it remains a challenge to solve water-accelerated fatigue of lubricating oils owing to the poor mechanical durability of superhydrophobic surfaces and the intractable emulsions stabilized by additives. In this work, a robust superhydrophobic membrane for solving water-accelerated fatigue of lubricating oils containing zinc dialkyldithiophosphate (ZDDP) as a typical antiwear additive is presented. An all-inorganic coating is constructed by SiO

Switching between superhydrophobicity/underwater superoleophilicity and superhydrophilicity/underwater superoleophobicity has been widely designed. Recently, superwettability is subdivided into multiple extreme wetting states for oil, water, and air as wetting and medium phases. However, fine switching among the multiple superwettability is rare. Here, a pH-responsive case is presented to demonstrate the fine switching between underwater superoleophilicity and underwater superoleophobicity while maintaining superhydrophobicity. The surface chemistry of silver-roughened copper coatings is elaborately manipulated by water-repellent perfluoroalkyl and alkyl chains and the smart terminal carboxyl group. By adjusting the pH value of water, the completely opposite extreme wetting states for oil in water are precisely controlled. Simultaneously, the extreme repellence for water in the air can be kept owing to the fairly low surface energy of the perfluoroalkyl chain. This discovery accelerates the subdivision of superwettability and the achievement of unusual superwetting switching.

It is of great clinical significance to develop potential novel strategies to prevent diabetic cardiovascular complications. Endothelial progenitor cell (EPC) dysfunction is a key contributor to diabetic vascular complications. In the present study we evaluated whether low-dose nifedipine could rescue impaired EPC-mediated angiogenesis and prevent cardiovascular complications in diabetic mice. Diabetes was induced in mice by five consecutive injections of streptozotocin (STZ, 60 mg·kg

Transcription factors (TFs) specifically bind to DNA, recruit cofactor proteins and modulate target gene expression, rendering them essential roles in the regulation of numerous biological processes. Meanwhile, mutated or dysregulated TFs are involved in a variety of human diseases. As multiple signaling pathways ultimately converge at TFs, targeting these TFs directly may prove to be more specific and cause fewer side effects, than targeting the upfront conventional targets in these pathways. All these features together endue TFs with great potential and high selectivity as therapeutic drug targets. However, TFs have been historically considered "undruggable", mainly due to their lack of structural information, especially about the appropriate ligand-binding sites and protein-protein interactions, leading to relatively limited choices in the TF-targeting drug design. In this review, we summarize the recent progress of TF-targeting drugs and highlight certain strategies used for targeting TFs, with a number of representative drugs that have been approved or in the clinical trials as examples. Various approaches in targeting TFs directly or indirectly have been developed. Common direct strategies include aiming at defined binding pockets, proteolysis-targeting chimaera (PROTAC), and mutant protein reactivation. In contrast, the indirect ones comprise inhibition of protein-protein interactions between TF and other proteins, blockade of TF expression, targeting the post-translational modifications, and targeting the TF-DNA interactions. With more comprehensive structural information about TFs revealed by the powerful cryo-electron microscopy technology and predicted by machine-learning algorithms, plus more efficient compound screening platforms and a deeper understanding of TF-disease relationships, the development of TF-targeting drugs will certainly be accelerated in the near future.

Bcl-2 family proteins play an important role in regulation of the cell survival and death. The inhibition of the anti-apoptotic proteins of Bcl-2 family leads to the apoptosis of cancer. BH3 mimetics have been developed targeting anti-apoptotic proteins of Bcl-2 family as small molecular drugs. It has been proved that BH3 mimetics has effect on apoptosis and proliferation in leukemia and some of them has been used in phase one or two clinical trials. Besides, with the development of the research on autophagic cell death, the antagonism and the synergism of autophagy and apoptosis is significant in cell death. As a hub of these two pathways of cell death, Bcl-2 protein is a potential target in basic research and clinical applications. In our studies, we found 32 potential BH3 mimetics compounds from 140,000 small molecular compounds via pharmacophore-based virtual screening. Furthermore, we demonstrated SM3, one of the 32 potential BH3 mimetics, induced autophagy and apoptosis simultaneously in dose-time dependence in A549 cell. SM3 induced apoptosis by intrinsic apoptosis pathway and induced autophagy by weakening the interaction between Beclin-1 and Bcl-2 complex. We wish to provide evidences and clues for the structural optimizing and further study of new compounds in the future.

Superantiwettability has been developed from single to multiple extreme wetting states for one wetting phase under another medium phase among water, oil, and air. However, controllable preparation of multiple superantiwetting surfaces especially from dual to quadruple superlyophobicity is rare. Herein, a facile method is proposed to prepare (1) underwater superoleophobic and underoil superhydrophobic surface, (2) in-air superhydrophobic surface with the dual superlyophobicity in oil-water system, and (3) in-air superamphiphobic surface with the dual superlyophobicity in oil-water system. These multiple superantiwetting states from dual to quadruple superlyophobicity are realized by controlling the surface chemistry, i.e., simply adjusting the ratio of TiO2 nanoparticles and fluorocarbon surfactant in the spray solution. With minimum dosage of the fluorine-rich component, the dual superlyophobic surface can be used for on-demand oil-water separation. This discovery will promote the subdivision of superantiwettability in water-oil-air system to extend interfacial applications.

Anisotropic wetting properties of patterned surfaces are critical for fundamental research and potential applications. In spite of significant development in investigation of such surfaces, the importance of geometries parameter of the micro/nanostructure on anisotropic wettability is not understood completely, particularly in thermodynamic analysis aspect. In this work, a trapezoidal profile surfaces with hierarchical stripes were analyzed using a two-dimensional model by cutting a three-dimensional structure along a given orientation. According to the calculations of free energy and free energy barrier, the effects of cutting orientation and all the geometrical parameters for the surfaces on equilibrium contact angle (ECA) and contact angle hysteresis (CAH) were investigated systematically. It is demonstrated that the ECA and CAH are closely related to the cutting orientation and the trapezoidal base angle of hierarchical striped surfaces. In addition, the wetting state at the nanoscale facilitates the transition from isotropic to anisotropic ECA and CAH of the striped surfaces with Cassie-type state at the microscale. As for micro/nanostructured surfaces at Wenzel-type wetting state, the anisotropic behavior of ECA and CAH is further enhanced by the existence of nanostructures. These calculated results are well agreement with the related experimental results, which will provide fundamental principles for the design of demanded geometry of micro/nanostructured surfaces with controllable anisotropic wetting behavior.

In this article, we report the construction of semicircular micro/nanostructured surfaces. Based on thermodynamic analysis, free energy (FE) and free energy barrier (FEB) as well as equilibrium contact angle (ECA) and contact angle hysteresis (CAH) for four exact wetting states of semicircular micro/nanostructured surfaces are theoretically discussed in detail. Notably, the wetting behavior is closely related to the exact wetting state and the base radius or space of semicircular micro/nanostructure. Furthermore, it is demonstrated that the stable wetting state of the semicircular micro/nanostructured surfaces depends on the microscale and nanoscale ratio of base space and radius. A suitable semicircular micro/nanostructure of the surface may lead to a droplet in the stable Cassie-Cassie (Cc) state. Moreover, an important role of the nanoscale semicircular surfaces in determining water super-repellence is effective in decreasing or increasing the ratio of microscale base space and radius for the Cassie or Wenzel state. Additionally, wetting behaviour of single semicircular micro- and nano-structured surfaces are comparatively investigated. The FE and ECA of micro/nanostructured surfaces are lower or higher than those of the single microstructured surfaces. However, the effects of nanoscale semicircular surfaces on the FEB and CAH mainly rely on the microscale wetting state. Finally, the related experimental results were used to verify our investigation. These results are in good agreement with the experiment, which are helpful in designing the wetting behavior of hierarchical semicircular micro/nano-structured surface.

Superantiwetting surfaces with contact angles above 150° and sliding angles below 10° for one wetting phase under another medium phase among water, oil, and air have been designed. However, all superantiwetting surfaces that show super-repellence in any two-phase system including six extreme wetting states such as superhydrophobicity, superoleophobicity, underoil superhydrophobicity, underwater superoleophobicity, and underoil and underwater superaerophobicity are extremely rare. Here, we prepare all superantiwetting surfaces by simply spraying a suspension containing titanium dioxide, aluminum phosphate, and perfluorosilane on substrates. In a broad sense, the all superantiwetting state can be extended to polar liquid–nonpolar liquid–air systems. Thus, the prepared surfaces realize high-efficiency on-demand separation of immiscible organic liquids. This discovery opens up the possibility of multiple extreme wetting surfaces even involving a wide range of organic liquids.

Isothiazolinone (IT) biocides are potent antibacterial substances commonly used as preservatives or disinfectants, and 2-n-Octyl-4-isothiazolin-3-one (OIT, octhilinone) is a common IT biocide that is present in leather products, glue, paints, and cleaning products. Although humans are exposed to OIT through personal and industrial use, the potentially deleterious effects of OIT on human health are still unknown. To investigate the effects of OIT on the vascular system, which is continuously exposed to xenobiotics through systemic circulation, we treated brain endothelial cells with OIT. OIT treatment significantly activated caspase-3-mediated apoptosis and reduced the bioenergetic function of mitochondria in a bEnd.3 cell-based in vitro blood–brain barrier (BBB) model. Interestingly, OIT significantly altered the thiol redox status, as evidenced by reduced glutathione levels and protein S-nitrosylation. The endothelial barrier function of bEnd.3 cells was significantly impaired by OIT treatment. OIT affected mitochondrial dynamics through mitophagy and altered mitochondrial morphology in bEnd.3 cells. N-acetyl cysteine significantly reversed the effects of OIT on the metabolic capacity and endothelial function of bEnd.3 cells. Taken together, we demonstrated that the alteration of the thiol redox status and mitochondrial damage contributed to OIT-induced BBB dysfunction, and we hope that our findings will improve our understanding of the potential hazardous health effects of IT biocides.

Water is recognized as a contaminant in lubricating oils. Recently, interfacial materials with special wettability have been broadly developed for oil-water separation. However, solving lubricating oil failure caused by water remains a challenge. Here, a robust superhydrophobic membrane is presented to effectively remove water in lubricating oils to recover their lubricating capability. Compared to pure lubricating oils without or with an additive, lubricating oils collected from their emulsions using the superhydrophobic membrane have an equivalent friction coefficient and wear volume, which are much lower than that of lubricating oils contaminated by water. Water in lubricating oils accelerates the oxidation of metallic substrates and wear corrosion. Moreover, the metallic ions dissolved in water-containing lubricating oils induce the catalytic dehydrogenation of lubricating oils, leading to the deposition of a good deal of carbon-based wear debris. Importantly, the prepared membrane shows steady performance in regard to extreme water repellency, high-efficiency purification of lubricating oils, and low wear volume even after harsh mechanical damage. Robust interfacial materials have potential advantages in practically solving lubricating oil failure caused by water.

Acute kidney injury (AKI) is a serious threat to human health. Clinically, ischemia-reperfusion (I/R) injury is considered one of the most common contributors to AKI. Emodin has been reported to alleviate I/R injury in the heart, brain, and small intestine in rats and mice through its anti-inflammatory effects. The present study investigated whether emodin improved AKI induced by I/R and elucidated the molecular mechanisms. We used a mouse model of renal I/R injury and human renal tubular epithelial cell model of hypoxia/reoxygenation (H/R) injury. Ischemia/reperfusion resulted in renal dysfunction. Pretreatment with emodin ameliorated renal injury in mice following I/R injury. Emodin reduced mitochondrial-mediated apoptosis, suppressed the overproduction of mitochondrial reactive oxygen species and accelerated the recovery of adenosine triphosphate both in vivo and in vitro. Emodin prevented mitochondrial fission and restored the balance of mitochondrial dynamics. The phosphorylation of dynamin-related protein 1 (DRP1) at Ser616, a master regulator of mitochondrial fission, was upregulated in both models of I/R and H/R injury, and this upregulation was blocked by emodin. Using computational cognate protein kinase prediction and specific kinase inhibitors, we found that emodin inhibited the phosphorylation of calcium/calmodulin-dependent protein kinase II (https://www.guidetopharmacology.org/GRAC/ObjectDisplayForward?objectId=1554), thereby inhibiting its kinase activity and reducing the phosphorylation of DRP1 at Ser616. The results demonstrated that emodin pretreatment could protect renal function by improving mitochondrial dysfunction induced by I/R.

FAM3B, also known as PANcreatic DERived factor (PANDER), promotes gluconeogenesis and lipogenesis in hepatocytes. However, the underlying mechanism(s) still remains largely unclear. This study determined the mechanism of PANDER‐induced FOXO1 activation in hepatocytes. In mouse livers and cultured hepatocytes, PANDER protein is located in both the cytoplasm and nucleus. Nuclear PANDER distribution was increased in the livers of obese mice. In cultured mouse and human hepatocytes, PANDER was co‐localized with FOXO1 in the nucleus. PANDER directly interacted with FOXO1 in mouse and human hepatocytes. PANDER overexpression enhanced PANDER‐FOXO1 interaction, and detained FOXO1 in the nucleus upon insulin stimulation in hepatocytes. With the increase in PANDER‐FOXO1 interaction, PANDER overexpression upregulated the expression of gluconeogenic genes and promoted gluconeogenesis in both human and mouse hepatocytes. Luciferase reporter assays further revealed that PANDER augmented the transcriptional activity of FOXO1 on gluconeogenic genes. Moreover, PANDER overexpression also interfered the binding of AS1842856, a specific FOXO1 inhibitor, with FOXO1, and impaired its inhibitory effects on gluconeogenic gene expression and gluconeogenesis in hepatocytes. siRNA mediated‐silencing of FOXO1 inhibited PANDER‐promoted gluconeogenic gene expression and glucose production in hepatocytes. In conclusion, PANDER protein is abundantly present in the nucleus, where it functions as a new co‐activator of FOXO1 to induce gluconeogenic gene expression in hepatocytes.