The human endogenous retrovirus type W envelope glycoprotein(ERVWE1),located at chromosome 7q21–22,has been implicated in the pathophysiology of schizophrenia.Our previous studies have shown elevated ERVWE1 expressio...The human endogenous retrovirus type W envelope glycoprotein(ERVWE1),located at chromosome 7q21–22,has been implicated in the pathophysiology of schizophrenia.Our previous studies have shown elevated ERVWE1 expression in schizophrenia patients.Growing evidence suggests that autophagy dysfunction contributes to schizophrenia,yet the relationship between ERVWE1 and autophagy remains unclear.In this study,bioinformatics analysis of the human prefrontal cortex RNA microarray dataset(GSE53987)revealed that differentially expressed genes were predominantly enriched in autophagy-related pathways.Clinical data further demonstrated that serum levels of microtubuleassociated protein 1 light chain 3β(LC3B),a key marker of macroautophagy,were significantly elevated in schizophrenia patients compared to controls,and positively correlated with ERVWE1 expression.Cellular and molecular experiments suggested that ERVWE1 promoted macroautophagy by increasing the LC3B II/I ratio,enhancing autophagosome formation,and reducing sequestosome 1(SQSTM1)expression via upregulation of NADPH oxidase activator 1(NOXA1).Concurrently,NOXA1 downregulated the expression of key micromitophagy-related genes,including PTEN-induced kinase 1(PINK1),Parkin RBR E3 ubiquitin-protein ligase(Parkin),and the pyruvate dehydrogenase E1 subunitα1(PDHA1).As a result,ERVWE1,via NOXA1,inhibited micromitophagy by suppressing the expression of PINK1,Parkin,and PDHA1,thereby leading to impaired production of mitochondrialderived vesicles(MDVs).Mechanistically,ERVWE1 enhanced NOXA1 transcription by upregulating upstream transcription factor 2(USF2).In conclusion,ERVWE1 promotes macroautophagy and inhibits micromitophagy through USF2-NOXA1 axis,providing novel mechanistic insight into the role autophagy dysregulation in schizophrenia.These findings suggest that targeting autophagy pathways may offer novel therapeutic strategies for schizophrenia treatment.展开更多
基金supported by the National Natural Science Foundation of China(No.82272321)the Stanley Foundation from the Stanley Medical Research Institute(SMRI),United States(No.06R-1366)。
文摘The human endogenous retrovirus type W envelope glycoprotein(ERVWE1),located at chromosome 7q21–22,has been implicated in the pathophysiology of schizophrenia.Our previous studies have shown elevated ERVWE1 expression in schizophrenia patients.Growing evidence suggests that autophagy dysfunction contributes to schizophrenia,yet the relationship between ERVWE1 and autophagy remains unclear.In this study,bioinformatics analysis of the human prefrontal cortex RNA microarray dataset(GSE53987)revealed that differentially expressed genes were predominantly enriched in autophagy-related pathways.Clinical data further demonstrated that serum levels of microtubuleassociated protein 1 light chain 3β(LC3B),a key marker of macroautophagy,were significantly elevated in schizophrenia patients compared to controls,and positively correlated with ERVWE1 expression.Cellular and molecular experiments suggested that ERVWE1 promoted macroautophagy by increasing the LC3B II/I ratio,enhancing autophagosome formation,and reducing sequestosome 1(SQSTM1)expression via upregulation of NADPH oxidase activator 1(NOXA1).Concurrently,NOXA1 downregulated the expression of key micromitophagy-related genes,including PTEN-induced kinase 1(PINK1),Parkin RBR E3 ubiquitin-protein ligase(Parkin),and the pyruvate dehydrogenase E1 subunitα1(PDHA1).As a result,ERVWE1,via NOXA1,inhibited micromitophagy by suppressing the expression of PINK1,Parkin,and PDHA1,thereby leading to impaired production of mitochondrialderived vesicles(MDVs).Mechanistically,ERVWE1 enhanced NOXA1 transcription by upregulating upstream transcription factor 2(USF2).In conclusion,ERVWE1 promotes macroautophagy and inhibits micromitophagy through USF2-NOXA1 axis,providing novel mechanistic insight into the role autophagy dysregulation in schizophrenia.These findings suggest that targeting autophagy pathways may offer novel therapeutic strategies for schizophrenia treatment.
