TY - JOUR
T1 - Sox9-Positive Progenitor Cells Play a Key Role in Renal Tubule Epithelial Regeneration in Mice
AU - Kang, Hyun Mi
AU - Huang, Shizheng
AU - Reidy, Kimberly
AU - Han, Seung Hyeok
AU - Chinga, Frank
AU - Susztak, Katalin
N1 - Funding Information:
Work in the K.S. lab is supported by NIH DK076077. H.M.K. is supported by a post-doctoral fellowship form the Juvenile Diabetes Research Foundation (3-2013-182). We would like to thank Dr. Dong Zheng and his lab members (Georgia Health Science Center) for helping with the ischemia/reperfusion experiments and Dr. Mariya Sweetwyne for helping with some of the animal experiments.
Publisher Copyright:
© 2016 The Authors.
PY - 2016/2/2
Y1 - 2016/2/2
N2 - The kidney has a tremendous capacity to regenerate following injury, but factors that govern this response are still largely unknown. We isolated cells from mouse kidneys with high proliferative and multi-lineage differentiation capacity. These cells expressed a high level of Sox9. In regenerating kidneys, Sox9 expression was induced early, and 89% of proliferating cells were Sox9 positive. In vitro, Sox9-positive cells showed unlimited proliferation and multi-lineage differentiation capacity. Using an inducible Sox9 Cre line and lineage-tagging methods, we show that Sox9-positive cells can generate new daughter cells, contributing to the regeneration of proximal tubule, loop of Henle, and distal tubule segments but not to collecting duct and glomerular cells. Furthermore, inducible deletion of Sox9 resulted in reduced epithelial proliferation, more severe injury, and fibrosis development. In summary, we demonstrate that, in the kidney, Sox9-positive cells show progenitor-like properties in vitro and contribute to epithelial regeneration following injury in vivo.
AB - The kidney has a tremendous capacity to regenerate following injury, but factors that govern this response are still largely unknown. We isolated cells from mouse kidneys with high proliferative and multi-lineage differentiation capacity. These cells expressed a high level of Sox9. In regenerating kidneys, Sox9 expression was induced early, and 89% of proliferating cells were Sox9 positive. In vitro, Sox9-positive cells showed unlimited proliferation and multi-lineage differentiation capacity. Using an inducible Sox9 Cre line and lineage-tagging methods, we show that Sox9-positive cells can generate new daughter cells, contributing to the regeneration of proximal tubule, loop of Henle, and distal tubule segments but not to collecting duct and glomerular cells. Furthermore, inducible deletion of Sox9 resulted in reduced epithelial proliferation, more severe injury, and fibrosis development. In summary, we demonstrate that, in the kidney, Sox9-positive cells show progenitor-like properties in vitro and contribute to epithelial regeneration following injury in vivo.
UR - http://www.scopus.com/inward/record.url?scp=84958111127&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84958111127&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2015.12.071
DO - 10.1016/j.celrep.2015.12.071
M3 - Article
C2 - 26776520
AN - SCOPUS:84958111127
SN - 2211-1247
VL - 14
SP - 861
EP - 871
JO - Cell Reports
JF - Cell Reports
IS - 4
ER -