Reports suggest a role of endothelial dysfunction and loss of endothelial barrier function in COVID-19. It is well established that the endothelial glycocalyx-degrading enzyme heparanase contributes to vascular leakage and inflammation. Low molecular weight heparins (LMWH) serve as an inhibitor of heparanase. We hypothesize that heparanase contributes to the pathogenesis of COVID-19, and that heparanase may be inhibited by LMWH. To test this hypothesis, heparanase activity and heparan sulfate levels were measured in plasma of healthy controls (n = 10) and COVID-19 patients (n = 48). Plasma heparanase activity and heparan sulfate levels were significantly elevated in COVID-19 patients. Heparanase activity was associated with disease severity including the need for intensive care, lactate dehydrogenase levels, and creatinine levels. Use of prophylactic LMWH in non-ICU patients was associated with a reduced heparanase activity. Since there is no other clinically applied heparanase inhibitor currently available, therapeutic treatment of COVID-19 patients with low molecular weight heparins should be explored.
Reports suggest a role of endothelial dysfunction and loss of endothelial barrier function in COVID-19. It is well established that the endothelial glycocalyx-degrading enzyme heparanase contributes to vascular leakage and inflammation. Low molecular weight heparins (LMWH) serve as an inhibitor of heparanase. We hypothesize that heparanase contributes to the pathogenesis of COVID-19, and that heparanase may be inhibited by LMWH. Heparanase activity and heparan sulfate levels were measured in plasma of healthy controls (n=10) and COVID-19 patients (n=48). Plasma heparanase activity and heparan sulfate levels were significantly elevated in COVID-19 patients. Heparanase activity associated with disease severity including the need for intensive care and mechanical ventilation, lactate dehydrogenase levels and creatinine levels. Use of prophylactic LMWH in non-ICU patients was associated with a reduced heparanase activity. Since there is no other clinically applied heparanase inhibitor currently available, therapeutic treatment of COVID-19 patients with low molecular weight heparins should be explored.
Mg2؉ is an essential ion for many cellular processes, including protein synthesis, nucleic acid stability, and numerous enzymatic reactions. Mg 2؉ homeostasis in mammals depends on the equilibrium between intestinal absorption, renal excretion, and exchange with bone. To maintain a physiological extra-and intracellular Mg 2ϩ concentration is of great importance to keep the accurate function of more than 300 enzymatic systems and the subsequent various biological and physiological processes (1-4). The kidney is the principal organ responsible for the regulation of the body Mg 2ϩ balance. Around 80% of the total plasma Mg 2ϩ is ultrafiltered through the glomeruli and subsequently reabsorbed passively in the proximal tubule and the thick ascending limb of Henle's loop (5 Ϫ/Ϫ mice that survived had neural tube defects (9). TRPM6 and its closest homologue TRPM7 uniquely combine an ion channel pore-forming region with a serine/ threonine protein kinase domain. It is located at the carboxyl terminus and has similarities with members of the ␣-kinase family (10,11). Previous studies demonstrated that receptor for activated C-kinase 1 (RACK1) and repressor of estrogen receptor activity (REA) interact with this domain and inhibit channel activity in an (auto)phosphorylation-dependent manner (12, 13). Moreover, modulation of TRPM6 channel activity by intracellular ATP requires the ATP-binding motif in the ␣-kinase domain (14). Although the phosphorylation activity of the TRPM6/7 ␣-kinase domains has been well determined, the role of these domains in regulating channel activity remains elusive (12,(15)(16)(17)(18).Over the last years, several studies have implicated TRPM channels in ischemia (19,20). Sun et al. (21) showed that decreased TRPM7 channel expression significantly reduced neuronal cell death after global ischemia. Furthermore, TRPM4 channel activation in vascular smooth muscle has been shown to contribute to cell death of vascular cells during ischemic injury, and TRPM2 has been well studied in relation to oxidative stress (22)(23)(24)(25). Accumulating evidence suggests that reactive oxygen species are not only harmful side products of cellular metabolism but also central players in cell signaling and regulation (26 -29). Interestingly, renal DCT cells contain the largest number of mitochondria. However, the effect of oxidative stress on the epithelial Mg 2ϩ channel TRPM6, expressed at the apical membrane of the DCT, has not been studied.The aim of the present study was to investigate the role of the ␣-kinase domain in TRPM6 channel activity by the identification of associated proteins. To this end, the Ras recruitment system (RRS), a novel yeast two-hybrid screening system, which is designed to screen for partners of plasma membrane proteins, was applied (30). Here, we identified methionine sulfoxide reductase B1 (MsrB1) as a TRPM6-associated protein, bind-
The thiazide-sensitive NaCl cotransporter (NCC) plays a key role in renal salt reabsorption and the determination of systemic BP, but the molecular mechanisms governing the regulation of NCC are not completely understood. Here, through pull-down experiments coupled to mass spectrometry, we found that ␥-adducin interacts with the NCC transporter. ␥-Adducin colocalized with NCC to the distal convoluted tubule.22 Na ϩ uptake experiments in the Xenopus laevis oocyte showed that ␥-adducin stimulated NCC activity in a dose-dependent manner, an effect that occurred upstream from With No Lysine (WNK) 4 kinase. The binding site of ␥-adducin mapped to the N terminus of NCC and encompassed three previously reported phosphorylation sites. Supporting this site of interaction, competition with the N-terminal domain of NCC abolished the stimulatory effect of ␥-adducin on the transporter. ␥-Adducin failed to increase NCC activity when these phosphorylation sites were constitutively inactive or active. In addition, ␥-adducin bound only to the dephosphorylated N terminus of NCC. Taken together, our observations suggest that ␥-adducin dynamically regulates NCC, likely by amending the phosphorylation state, and consequently the activity, of the transporter. These data suggest that ␥-adducin may influence BP homeostasis by modulating renal NaCl transport.
Highlights d PBMCs of COVID-19 patients show increased responses to Toll-like receptor ligands d Trained immunity is modeled in vitro using Candida-trained PBMCs d Hydroxychloroquine inhibits changes in lipidome and histone modifications d Hydroxychloroquine dampens the trained response to interferons and viral stimuli
The study of gene function at later stages of embryonic development by overexpression experiments is often complicated by genes exerting different functions at multiple stages of development, which renders analysis of stage-specific effects difficult. To address this problem an inducible expression system that supports timed expression of essentially any protein, including secreted proteins was designed. The system is based on a two step mechanism. A glucocorticoid inducible, Gal4-site binding chimeric transcription factor is expressed ubiquitously, whereas a gene of interest is placed under the control of a Gal4-site driven promoter. Treatment of zebrafish embryos injected with such constructs with the synthetic glucocorticoid dexamethasone results in readily detectable reporter activity within 3 h. The system was tested with induced expression of Xactivin(beta)B and X(wnt), which both were shown to induce morphological abnormalities, as well as alterations in the expression patterns of goosecoid and otx2, respectively. Coinjection of an inducible lacZ reporter vector served as an indicator for expressing cells in embryos. The present results demonstrate that this is a versatile inducible expression system for use in vertebrate embryos, that also supports expression of secreted proteins.
Complement dysregulation is characteristic of the renal diseases atypical hemolytic uremic syndrome (aHUS) and complement component 3 glomerulopathy (C3G). Complement regulatory protein Factor H (FH) inhibits complement activity, whereas FH-related proteins (FHRs) lack a complement regulatory domain. FH and FHRs compete for binding to host cell glycans, in particular heparan sulfates (HS). HS is a glycosaminoglycan with an immense structural variability, where distinct sulfation patterns mediate specific binding of proteins. Mutations in FH, FHRs, or an altered glomerular HS structure may disturb the FH : FHRs balance on glomerular endothelial cells, thereby leading to complement activation and the subsequent development of aHUS/C3G. In this study, we aimed to identify specific HS structures that could specifically compete off FHRs from HS glycocalyx (HSGlx), without interfering with FH binding. FH/FHR binding to human conditionally immortalized glomerular endothelial cells (ciGEnCs) and HSGlx purified from ciGEnC glycocalyx was assessed. HS modifications important for FH/FHR binding to HSGlx were analyzed using selectively desulfated heparins in competition with purified HSGlx. We further assessed effects of heparinoids on FHR1- and FHR5-mediated C3b deposition on ciGEnCs. In the presence of C3b, binding of FH, FHR1 and FHR5 to ciGEnCs was significantly increased, whereas binding of FHR2 was minimal. FHR1 and 5 competitively inhibited FH binding to HSGlx, leading to alternative pathway dysregulation. FHR1 and FHR5 binding was primarily mediated by N-sulfation while FH binding depended on N-, 2-O- and 6-O-sulfation. Addition of 2-O-desulfated heparin significantly reduced FHR1- and FHR5-mediated C3b deposition on ciGEnCs. We identify 2-O-desulfated heparin derivatives as potential therapeutics for C3G and other diseases with dysregulated complement.
SARS-CoV-2 infection can cause severe disease for which currently no specific therapy is available. The use of hydroxychloroquine to prevent or treat SARS-CoV-2 infection is controversial and its mode of action poorly understood. We demonstrate that hydroxychloroquine inhibits trained immunity at the functional and epigenetic level and is accompanied by profound changes in the cellular lipidome as well as reduced expression of interferon-stimulated genes. Trained immunity comprises a functional adaptation induced by epigenetic reprogramming which facilitates the anti-viral innate immune response. Our findings therefore suggest that hydroxychloroquine may not have a beneficial effect on the anti-viral immune response to SARS-CoV-2.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.