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Renal fibrosis: Primacy of the proximal tubule.

Gewin LS
Matrix Biol. 2018 68-69: 248-262

PMID: 29425694 · PMCID: PMC6015527 · DOI:10.1016/j.matbio.2018.02.006

Tubulointerstitial fibrosis (TIF) is the hallmark of chronic kidney disease and best predictor of renal survival. Many different cell types contribute to TIF progression including tubular epithelial cells, myofibroblasts, endothelia, and inflammatory cells. Previously, most of the attention has centered on myofibroblasts given their central importance in extracellular matrix production. However, emerging data focuses on how the response of the proximal tubule, a specialized epithelial segment vulnerable to injury, plays a central role in TIF progression. Several proximal tubular responses such as de-differentiation, cell cycle changes, autophagy, and metabolic changes may be adaptive initially, but can lead to maladaptive responses that promote TIF both through autocrine and paracrine effects. This review discusses the current paradigm of TIF progression and the increasingly important role of the proximal tubule in promoting TIF both in tubulointerstitial and glomerular injuries. A better understanding and appreciation of the role of the proximal tubule in TIF has important implications for therapeutic strategies to halt chronic kidney disease progression.

Copyright © 2018 International Society of Matrix Biology. Published by Elsevier B.V. All rights reserved.

MeSH Terms (9)

Animals Disease Progression Extracellular Matrix Fibrosis Humans Kidney Tubules, Proximal Macrophages Myofibroblasts Renal Insufficiency, Chronic

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