Chrysin inhibits diabetic renal tubulointerstitial fibrosis through blocking epithelial to mesenchymal transition

Verfasser / Beitragende:
[Min-Kyung Kang, Sin-Hye Park, Yean-Jung Choi, Daekeun Shin, Young-Hee Kang]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Molecular Medicine, 93/7(2015-07-01), 759-772
Format:
Artikel (online)
ID: 605543224
LEADER caa a22 4500
001 605543224
003 CHVBK
005 20210128100925.0
007 cr unu---uuuuu
008 210128e20150701xx s 000 0 eng
024 7 0 |a 10.1007/s00109-015-1301-3  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00109-015-1301-3 
245 0 0 |a Chrysin inhibits diabetic renal tubulointerstitial fibrosis through blocking epithelial to mesenchymal transition  |h [Elektronische Daten]  |c [Min-Kyung Kang, Sin-Hye Park, Yean-Jung Choi, Daekeun Shin, Young-Hee Kang] 
520 3 |a Renal fibrosis is a crucial event in the pathogenesis of diabetic nephropathy (DN). The process known as epithelial to mesenchymal transition (EMT) contributes to the accumulation of matrix proteins in kidneys, in which renal tubular epithelial cells play an important role in progressive renal fibrosis. The current study investigated that chrysin (5,7-dihydroxyflavone) present in bee propolis and herbs, inhibited renal tubular EMT and tubulointerstitial fibrosis due to chronic hyperglycemia. Human renal proximal tubular epithelial cells (RPTEC) were incubated in media containing 5.5mM glucose, 27.5mM mannitol (as an osmotic control), or 33mM glucose (HG) in the absence and presence of 1-20μM chrysin for 72h. Chrysin significantly inhibited high glucose-induced renal EMT through blocking expression of the mesenchymal markers vimentin, α-smooth muscle actin, and fibroblast-specific protein-1 in RPTEC and db/db mice. Chrysin reversed the HG-induced down-regulation of the epithelial marker E-cadherin and the HG-enhanced N-cadherin induction in RPTEC. In addition, chrysin inhibited the production of collagen IV in tubular cells and the deposition of collagen fibers in mouse kidneys. Furthermore, chrysin blocked tubular cell migration concurrent with decreasing matrix metalloproteinase-2 activity, indicating epithelial cell derangement and tubular basement membrane disruption. Chrysin restored the induction of the tight junction proteins Zona occludens protein-1 (ZO-1) and occludin downregulated in diabetic mice. Chrysin inhibited renal tubular EMT-mediated tubulointerstitial fibrosis caused by chronic hyperglycemia. Therefore, chrysin may be a potent renoprotective agent for the treatment of renal fibrosis-associated DN. Key messages: • Glucose increases renal tubular epithelial induction of vimentin, α-SMA and FSP-1. • Glucose enhances renal EMT by blocking tubular epithelial E-cadherin expression. • Chrysin inhibits tubular EMT-mediated tubulointerstitial fibrosis in mouse kidneys. • Chrysin restores renal tubular induction of ZO-1 and occludin downregulated in diabetic mice. • Chrysin blocks glucose-induced renal tubular cell migration with reducing MMP-2 activity. 
540 |a Springer-Verlag Berlin Heidelberg, 2015 
690 7 |a Chrysin  |2 nationallicence 
690 7 |a Diabetic nephropathy  |2 nationallicence 
690 7 |a Epithelial to mesenchymal transition  |2 nationallicence 
690 7 |a High glucose  |2 nationallicence 
690 7 |a Tubulointerstitial fibrosis  |2 nationallicence 
690 7 |a CTGF : Connective tissue growth factor  |2 nationallicence 
690 7 |a DN : Diabetic nephropathy  |2 nationallicence 
690 7 |a ECM : Extracellular matrix  |2 nationallicence 
690 7 |a EMT : Epithelial to mesenchymal transition  |2 nationallicence 
690 7 |a FSP-1 : Fibroblast-specific protein  |2 nationallicence 
690 7 |a MT1-MMP : Membrane type 1-matrix metalloproteinase  |2 nationallicence 
690 7 |a RPTEC : Human renal proximal tubular epithelial cells  |2 nationallicence 
690 7 |a α-SMA : α-smooth muscle actin  |2 nationallicence 
690 7 |a TIMP-2 : Tissue inhibitor of metalloproteinase-2  |2 nationallicence 
690 7 |a ZO-1 : Zona occludens protein-1  |2 nationallicence 
700 1 |a Kang  |D Min-Kyung  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
700 1 |a Park  |D Sin-Hye  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
700 1 |a Choi  |D Yean-Jung  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
700 1 |a Shin  |D Daekeun  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
700 1 |a Kang  |D Young-Hee  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
773 0 |t Journal of Molecular Medicine  |d Springer Berlin Heidelberg  |g 93/7(2015-07-01), 759-772  |x 0946-2716  |q 93:7<759  |1 2015  |2 93  |o 109 
856 4 0 |u https://doi.org/10.1007/s00109-015-1301-3  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00109-015-1301-3  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kang  |D Min-Kyung  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Park  |D Sin-Hye  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Choi  |D Yean-Jung  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Shin  |D Daekeun  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kang  |D Young-Hee  |u Department of Food and Nutrition, Hallym University, 200-702, Chuncheon, Kangwon-do, Republic of Korea  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Molecular Medicine  |d Springer Berlin Heidelberg  |g 93/7(2015-07-01), 759-772  |x 0946-2716  |q 93:7<759  |1 2015  |2 93  |o 109