Literature DB >> 26494984

Role of upstream stimulatory factor 2 in diabetic nephropathy.

Shuxia Wang1.   

Abstract

Diabetic nephropathy (DN) is the most common cause of end-stage renal disease (ESRD). About 20%-30% of people with type 1 and type 2 diabetes develop DN. DN is characterized by both glomerulosclerosis with thickening of the glomerular basement membrane and mesangial matrix expansion, and tubulointerstitial fibrosis. Hyperglycemia and the activation of the intra-renal renin-angiotensin system (RAS) in diabetes have been suggested to play a critical role in the pathogenesis of DN. However, the mechanisms are not well known. Studies from our laboratory demonstrated that the transcription factor-upstream stimulatory factor 2 (USF2) is an important regulator of DN. Moreover, the renin gene is a downstream target of USF2. Importantly, USF2 transgenic (Tg) mice demonstrate a specific increase in renal renin expression and angiotensin II (AngII) levels in kidney and exhibit increased urinary albumin excretion and extracellular matrix deposition in glomeruli, supporting a role for USF2 in the development of diabetic nephropathy. In this review, we summarize our findings of the mechanisms by which diabetes regulates USF2 in kidney cells and its role in regulation of renal renin-angiotensin system and the development of diabetic nephropathy.

Entities:  

Keywords:  TGF-β; USF2; renal fibrosis; renin-angiotensin system

Year:  2015        PMID: 26494984      PMCID: PMC4610405          DOI: 10.1007/s11515-015-1359-x

Source DB:  PubMed          Journal:  Front Biol (Beijing)        ISSN: 1674-7984


  112 in total

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Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

Review 2.  Role of angiotensin II in diabetic nephropathy.

Authors:  D J Leehey; A K Singh; N Alavi; R Singh
Journal:  Kidney Int Suppl       Date:  2000-09       Impact factor: 10.545

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Journal:  J Biol Chem       Date:  1994-10-28       Impact factor: 5.157

Review 4.  The key role of the transforming growth factor-beta system in the pathogenesis of diabetic nephropathy.

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Journal:  Ren Fail       Date:  2001 May-Jul       Impact factor: 2.606

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Authors:  Rathinam Vasanthakumar; Viswanathan Mohan; Gowrisankar Anand; Mohan Deepa; Subash Babu; Vivekanandhan Aravindhan
Journal:  Cytokine       Date:  2014-12-23       Impact factor: 3.861

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Journal:  J Biol Chem       Date:  1997-08-29       Impact factor: 5.157

Review 7.  Diabetic nephropathy: mechanisms of renal disease progression.

Authors:  Yashpal S Kanwar; Jun Wada; Lin Sun; Ping Xie; Elisabeth I Wallner; Sheldon Chen; Sumant Chugh; Farhad R Danesh
Journal:  Exp Biol Med (Maywood)       Date:  2008-01

8.  Glucose up-regulates thrombospondin 1 gene transcription and transforming growth factor-beta activity through antagonism of cGMP-dependent protein kinase repression via upstream stimulatory factor 2.

Authors:  Shuxia Wang; Jim Skorczewski; Xu Feng; Lin Mei; Joanne E Murphy-Ullrich
Journal:  J Biol Chem       Date:  2004-06-07       Impact factor: 5.157

9.  Neutralization of TGF-beta by anti-TGF-beta antibody attenuates kidney hypertrophy and the enhanced extracellular matrix gene expression in STZ-induced diabetic mice.

Authors:  K Sharma; Y Jin; J Guo; F N Ziyadeh
Journal:  Diabetes       Date:  1996-04       Impact factor: 9.461

Review 10.  Diabetic nephropathy - complications and treatment.

Authors:  Andy Kh Lim
Journal:  Int J Nephrol Renovasc Dis       Date:  2014-10-15
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  1 in total

Review 1.  TGF-β1-p53 cooperativity regulates a profibrotic genomic program in the kidney: molecular mechanisms and clinical implications.

Authors:  Craig E Higgins; Jiaqi Tang; Badar M Mian; Stephen P Higgins; Cody C Gifford; David J Conti; Kirstan K Meldrum; Rohan Samarakoon; Paul J Higgins
Journal:  FASEB J       Date:  2019-07-06       Impact factor: 5.834

  1 in total

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