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dc.contributor.author하헌주*
dc.date.accessioned2016-08-28T10:08:09Z-
dc.date.available2016-08-28T10:08:09Z-
dc.date.issued2012*
dc.identifier.issn0168-8227*
dc.identifier.otherOAK-9536*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223250-
dc.description.abstractAims: The present study examined renoprotective effect of human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSC) in diabetes. NRK-52E cells were utilized to determine the paracrine effect of hUCB-MSC. Methods: hUCB was harvested with the mother's consent. MSC obtained from the hUCB were injected through the tail vein. Growth arrested and synchronized NRK-52E cells were stimulated with transforming growth factor-β1 (TGF-β1) in the presence of hUCB-MSC conditioned media. Results: At 4 weeks after the streptozotocin (STZ) injection, diabetic rats showed significantly increased urinary protein excretion, renal and glomerular hypertrophy, fractional mesangial area, renal expression of TGF-β1 and α-smooth muscle actin, and collagen accumulation but decreased renal E-cadherin and bone morphogenic protein-7 expression, confirming diabetic renal injury. hUCB-MSC effectively prevented diabetic renal injury except renal and glomerular hypertrophy without a significant effect on blood glucose. CM-DiI-labeled hUCB-MSC and immunostaining of PKcs, a human nuclei antigen, confirmed a few engraftment of hUCB-MSC in diabetic kidneys. hUCB-MSC conditioned media inhibited TGF-β1-induced extracellular matrix upregulation and epithelial-to-mesenchymal transition in NRK-52E cells in a concentration-dependent manner. Conclusions: These results demonstrate the renoprotective effect of hUCB-MSC in STZ-induced diabetic rats possibly through secretion of humoral factors and suggest hUCB-MSC as a possible treatment modality for diabetic renal injury. © 2012 Elsevier Ireland Ltd.*
dc.languageEnglish*
dc.titleHuman umbilical cord blood-derived mesenchymal stem cells prevent diabetic renal injury through paracrine action*
dc.typeArticle*
dc.relation.issue3*
dc.relation.volume98*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage465*
dc.relation.lastpage473*
dc.relation.journaltitleDiabetes Research and Clinical Practice*
dc.identifier.doi10.1016/j.diabres.2012.09.034*
dc.identifier.wosidWOS:000312133700020*
dc.identifier.scopusid2-s2.0-84870673962*
dc.author.googlePark J.H.*
dc.author.googleHwang I.*
dc.author.googleHwang S.H.*
dc.author.googleHan H.*
dc.author.googleHa H.*
dc.contributor.scopusid하헌주(7202277106)*
dc.date.modifydate20240123091420*
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약학대학 > 약학과 > Journal papers
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