Transglutaminase Inhibition Reduces Fibrosis and Preserves Function in Experimental Chronic Kidney Disease
Author(s) -
Timothy S. Johnson,
Marie Fisher,
J. Haylor,
Zoe Hau,
Nicholas J. Skill,
Richard A. Jones,
Robert E. Saint,
I I Coutts,
Melissa E. Vickers,
A. Meguid El Nahas,
Martin Griffin
Publication year - 2007
Publication title -
journal of the american society of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.451
H-Index - 279
eISSN - 1533-3450
pISSN - 1046-6673
DOI - 10.1681/asn.2006070690
Subject(s) - tissue transglutaminase , kidney disease , fibrosis , renal function , medicine , function (biology) , kidney , disease , endocrinology , chemistry , biology , enzyme , biochemistry , microbiology and biotechnology
Progressive tissue fibrosis is involved in debilitating diseases that affect organs including the lungs, liver, heart, skin, and kidneys. Recent evidence suggests that tissue transglutaminase, an enzyme that crosslinks proteins, may be involved in tissue fibrosis by crosslinking and stabilizing the extracellular matrix or by recruiting and activating the large latent transforming growth factor (TGF)-1 complex. We treated rats that had undergone 5/6-nephrectomy with two different irreversible inhibitors of transglu- taminase and found that both prevented a decline in kidney function and reduced the development of glomerulosclerosis and tubulointerstitial fibrosis by up to 77% and 92%, respectively. Treatment reduced the accumulation of collagen I and collagen III, with the primary mechanism of action being direct interference with the crosslinking of extracellular matrix rather than altered regulation of TGF1. We conclude that inhibition of transglutaminase offers a potential therapeutic option for chronic kidney disease and other conditions that result from tissue fibrosis.
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