TY - JOUR
T1 - Renal fibrosis
T2 - Primacy of the proximal tubule
AU - Gewin, Leslie S.
N1 - Funding Information:
This work was supported in part by the National Institutes of Health Grant RO1-DK108968-01 .
Publisher Copyright:
© 2018 International Society of Matrix Biology
PY - 2018/8
Y1 - 2018/8
N2 - 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.
AB - 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.
KW - Cell cycle
KW - Chronic kidney disease
KW - Epithelial de-differentiation
KW - Metabolism
KW - Proteinuria
KW - Tubulointerstitial fibrosis
UR - http://www.scopus.com/inward/record.url?scp=85041964315&partnerID=8YFLogxK
U2 - 10.1016/j.matbio.2018.02.006
DO - 10.1016/j.matbio.2018.02.006
M3 - Review article
C2 - 29425694
AN - SCOPUS:85041964315
SN - 0945-053X
VL - 68-69
SP - 248
EP - 262
JO - Matrix Biology
JF - Matrix Biology
ER -