Full metadata record
DC Field | Value | Language |
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dc.contributor.author | 이용구 | - |
dc.date.accessioned | 2018-03-11T01:22:26Z | - |
dc.date.available | 2018-03-11T01:22:26Z | - |
dc.date.issued | 2013-10 | - |
dc.identifier.citation | PLOS ONE,2013,8(10) p1-10 | en_US |
dc.identifier.issn | 1932-6203 | - |
dc.identifier.uri | http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0077048 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11754/44832 | - |
dc.description.abstract | Background: The protective effects of granulocyte colony-stimulating factor (G-CSF) have been demonstrated in a variety of renal disease models. However, the influence of G-CSF on diabetic nephropathy (DN) remains to be examined. In this study, we investigated the effect of G-CSF on DN and its possible mechanisms in a rat model.Methods: Otsuka Long-Evans Tokushima Fatty (OLETF) rats with early DN were administered G-CSF or saline intraperitoneally. Urine albumin creatinine ratio (UACR), creatinine clearance, mesangial matrix expansion, glomerular basement membrane (GBM) thickness, and podocyte foot process width (FPW) were measured. The levels of interleukin (IL)-1 beta, transforming growth factor (TGF)-beta 1, and type IV collagen genes expression in kidney tissue were also evaluated. To elucidate the mechanisms underlying G-CSF effects, we also assessed the expression of G-CSF receptor (G-CSFR) in glomeruli as well as mobilization of bone marrow (BM) cells to glomeruli using sex-mismatched BM transplantation.Results: After four weeks of treatment, UACR was lower in the G-CSF treatment group than in the saline group (p<0.05), as were mesangial matrix expansion, GBM thickness, and FPW (p<0.05). In addition, the expression of TGF-beta 1 and type IV collagen and IL-1 beta levels was lower in the G-CSF treatment group (p<0.05). G-CSFR was not present in glomerular cells, and G-CSF treatment increased the number of BM-derived cells in glomeruli (p<0.05).Conclusions: G-CSF can prevent the progression of DN in OLETF rats and its effects may be due to mobilization of BM cells rather than being a direct effect. | en_US |
dc.description.sponsorship | Conceived and designed the experiments: KSK BIS. Performed theexperiments: BIS YSS CHF JYP. Analyzed the data: YSS KSK HK | en_US |
dc.language.iso | en | en_US |
dc.publisher | PUBLIC LIBRARY SCIENCE, 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA | en_US |
dc.subject | COLONY-STIMULATING FACTOR | en_US |
dc.subject | BONE-MARROW-TRANSPLANTATION | en_US |
dc.subject | ACUTE MYOCARDIAL-INFARCTION | en_US |
dc.subject | FOOT PROCESS EFFACEMENT | en_US |
dc.subject | STEM-CELL MOBILIZATION | en_US |
dc.subject | VERSUS-HOST-DISEASE | en_US |
dc.subject | OLETF RATS | en_US |
dc.subject | EXTRACELLULAR-MATRIX | en_US |
dc.subject | RENAL-DISEASE | en_US |
dc.subject | TGF-BETA | en_US |
dc.title | G-CSF prevents progression of diabetic nephropathy in rat | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1371/journal.pone.0077048 | - |
dc.relation.journal | PLOS ONE | - |
dc.contributor.googleauthor | So, Byung-Im | - |
dc.contributor.googleauthor | Song, Yi-Sun | - |
dc.contributor.googleauthor | Fang, Cheng-Hu | - |
dc.contributor.googleauthor | Park, Jun-Young | - |
dc.contributor.googleauthor | Lee, Yong-Gu | - |
dc.contributor.googleauthor | Shin, Jeong-Hun | - |
dc.contributor.googleauthor | Kim, Hyuck | - |
dc.contributor.googleauthor | Kim, Kyung-Soo | - |
dc.relation.code | 2013007124 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF MEDICINE[S] | - |
dc.sector.department | DEPARTMENT OF MEDICINE | - |
dc.identifier.pid | hmedi97 | - |
dc.identifier.researcherID | 54394133000 | - |
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