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10.1186/s12882-016-0348-x http://scihub22266oqcxt.onion/10.1186/s12882-016-0348-x C5028988!5028988 !27649757     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27649757 &cmd=llinks): Failed to open stream: HTTP request failed! 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Relationship of clusterin with renal inflammation and fibrosis after the recovery phase of ischemia-reperfusion injury |pdf=|usr=}}{{27649757 }} gab.com Text Relationship of clusterin with renal inflammation and fibrosis after the recovery phase of ischemia-reperfusion injury JO: BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=27649757 #FOAvip BACKGROUND: Long-term outcomes after acute kidney injury (AKI) include incremental loss of function and progression towards chronic kidney disease (CKD); however, the pathogenesis of AKI to CKD remains largely unknown. Clusterin (CLU) is a chaperone-like protein that reduces ischemia-reperfusion injury (IRI) and enhances tissue repair after IRI in the kidney. This study investigated the role of CLU in the transition of IRI to renal fibrosis. METHODS: IRI was induced in the left kidneys of wild type (WT) C57BL/6J (B6) versus CLU knockout (KO) B6 mice by clamping the renal pedicles for 28 min at the body temperature of 32 °C. Tissue damage was examined by histology, infiltrate phenotypes by flow cytometry analysis, and fibrosis-related gene expression by PCR array. RESULTS: Reduction of kidney weight was induced by IRI, but was not affected by CLU KO. Both WT and KO kidneys had similar function with minimal cellular infiltration and fibrosis at day 14 of reperfusion. After 30 days, KO kidneys had greater loss in function than WT, indicated by the higher levels of both serum creatinine and BUN in KO mice, and exhibited more cellular infiltration (CD8 cells and macrophages), more tubular damage and more severe tissue fibrosis (glomerulopathy, interstitial fibrosis and vascular fibrosis). PCR array showed the association of CLU deficiency with up-regulation of CCL12, Col3a1, MMP9 and TIMP1 and down-regulation of EGF in these kidneys. CONCLUSION: Our data suggest that CLU deficiency worsens renal inflammation and tissue fibrosis after IRI in the kidney, which may be mediated through multiple pathways. Twit Text FOAVip Relationship of clusterin with renal inflammation and fibrosis after the recovery phase of ischemia-reperfusion injury ????BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=27649757 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27649757 #FOAvip English Wikipedia <ref>{{Cite pmid|27649757 }}</ref> Relationship of clusterin with renal inflammation and fibrosis after the recovery phase of ischemia-reperfusion injury #MMPMID27649757 Guo J ; Guan Q ; Liu X ; Wang H ; Gleave ME ; Nguan CY ; Du C BMC Nephrol 2016[Sep]; 17 (1 ): 133 PMID27649757 show ga BACKGROUND: Long-term outcomes after acute kidney injury (AKI) include incremental loss of function and progression towards chronic kidney disease (CKD); however, the pathogenesis of AKI to CKD remains largely unknown. Clusterin (CLU) is a chaperone-like protein that reduces ischemia-reperfusion injury (IRI) and enhances tissue repair after IRI in the kidney. This study investigated the role of CLU in the transition of IRI to renal fibrosis. METHODS: IRI was induced in the left kidneys of wild type (WT) C57BL/6J (B6) versus CLU knockout (KO) B6 mice by clamping the renal pedicles for 28 min at the body temperature of 32 °C. Tissue damage was examined by histology, infiltrate phenotypes by flow cytometry analysis, and fibrosis-related gene expression by PCR array. RESULTS: Reduction of kidney weight was induced by IRI, but was not affected by CLU KO. Both WT and KO kidneys had similar function with minimal cellular infiltration and fibrosis at day 14 of reperfusion. After 30 days, KO kidneys had greater loss in function than WT, indicated by the higher levels of both serum creatinine and BUN in KO mice, and exhibited more cellular infiltration (CD8 cells and macrophages), more tubular damage and more severe tissue fibrosis (glomerulopathy, interstitial fibrosis and vascular fibrosis). PCR array showed the association of CLU deficiency with up-regulation of CCL12, Col3a1, MMP9 and TIMP1 and down-regulation of EGF in these kidneys. CONCLUSION: Our data suggest that CLU deficiency worsens renal inflammation and tissue fibrosis after IRI in the kidney, which may be mediated through multiple pathways. |Animals [MESH] |Biomarkers/metabolism [MESH] |Clusterin/*deficiency [MESH] |Fibrosis [MESH] |Male [MESH] |Mice [MESH] |Mice, Inbred C57BL [MESH] |Mice, Knockout [MESH] |Nephritis/*metabolism/*pathology [MESH] |Recovery of Function/*physiology [MESH]Relationship of clusterin with renal inflammation and fibrosis after t(epmc).pdf DeepDyve Pubget Overpricing