Tumor suppressor ataxia telangiectasia mutated functions downstream of TGF‐β1 in orchestrating profibrotic responses. Issue 4 (5th December 2014)

• Record Type: Journal Article
• Authors: Overstreet, Jessica M.; Samarakoon, Rohan; Cardona‐Grau, Diana; Goldschmeding, Roel; Higgins, Paul J.
• Is Part Of: FASEB journal. Volume 29:Issue 4(2015)
• Page Start: 1258
• Page End: 1268
• Publication Date: 2014-12-05
• Subjects: kidney fibrosis -- p53 · ROS -- NOX; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.14-262527
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Effective therapy to prevent organ fibrosis, which is associated with more than half of all mortalities, remains elusive. Involvement of tumor suppressor ataxia telangiectasia mutated (ATM) in the TGF‐β1 pathway related to renal fibrosis is largely unknown. ATM activation (pATM Ser1981 ) increased 4‐fold in the tubulointerstitial region of the unilateral ureteral obstruction‐injured kidney in mice correlating with SMAD3 and p53 Ser15 phosphorylation and elevated levels of p22 phox subunit of the NADPH oxidases (NOXs), and fibrotic markers, plasminogen activator inhibitor‐1 (PAI‐1), and fibronectin, when compared to contralateral (contra) or sham controls. In fact, ATM is rapidly phosphorylated at Ser 1981 by TGF‐b1 stimulation. Stable silencing and pharmacologic inhibition of ATM ablated TGF‐β1‐induced p53 activation (>95%) and subsequent PAI‐1, fibronectin, connective tissue growth factor, and p21 expression in human kidney 2 (HK‐2) tubular epithelial cells and normal rat kidney‐49 fibroblasts (NRK‐49F). ATM or p53 depletion in HK‐2 cells, moreover, bypassed TGF‐β1‐mediated cytostasis evident in control short hairpin RNA‐expressing HK‐2 cells. Interestingly, stable silencing of NOX subunits, p22 phox and p47 phox, in HK‐2 cells blocked TGF‐β1‐induced pATM Ser1981 (>90%) and target gene induction via p53‐dependent mechanisms. Furthermore, NRK‐49F fibroblast proliferation triggered by conditioned media from TGF‐β1‐stimulated, control vector‐transfected HK‐2 cells decreased (~50%) when exposed to conditioned media from ATM‐deficient, TGF‐β1‐treated HK‐2 cells. Thus, TGF‐β1 promotes NOX‐dependent ATM activation leading to p53‐mediated fibrotic gene reprogramming and growth arrest in HK‐2 cells. Furthermore, TGF‐β1/ATM‐initiated paracrine factor secretion by dysfunctional renal epithelium promotes interstitial fibroblast growth, suggesting a role of tubular ATM in mediating epithelial‐mesenchymal cross‐talk highlighting the translational benefit of targeting the NOX/ATM/p53 axis in renal fibrosis.—Overstreet, J. M., Samarakoon, R., Cardona‐Grau, D., Goldschmeding, R., Higgins, P. J. Tumor suppressor ataxia telangiectasia mutated functions downstream of TGF‐β1 in orchestrating profibrotic responses. FASEB J. 29, 1258‐1268 (2015). www.fasebj.org