| Literature DB >> 26776520 |
Hyun Mi Kang1, Shizheng Huang1, Kimberly Reidy1, Seung Hyeok Han1, Frank Chinga1, Katalin Susztak2.
Abstract
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.Entities:
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Year: 2016 PMID: 26776520 PMCID: PMC4854207 DOI: 10.1016/j.celrep.2015.12.071
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423