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Regenerative Role of Lrig1 + Cells in Kidney Repair

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Abstract
BackgroundIn response to severe kidney injury, the kidney epithelium displays remarkable regenerative capabilities driven by adaptable resident epithelial cells. To date, it has been widely considered that the adult kidney lacks multipotent stem cells; thus, the cellular lineages responsible for repairing proximal tubule damage are incompletely understood. Leucine-rich repeats and immunoglobulin-like domain protein 1-expressing cells (Lrig1+ cells) have been identified as a long-lived cell in various tissues that can induce epithelial tissue repair. Therefore, we hypothesized that Lrig1+ cells participate in kidney development and tissue regeneration.MethodsWe investigated the role of Lrig1+ cells in kidney injury using mouse models. The localization of Lrig1+ cells in the kidney was examined throughout mouse development. The function of Lrig1+ progeny cells in AKI repair was examined in vivo using a tamoxifen-inducible Lrig1-specific Cre recombinase-based lineage tracing in three different kidney injury mouse models. In addition, we conducted single-cell RNA sequencing to characterize the transcriptional signature of Lrig1+ cells and trace their progeny.ResultsLrig1+ cells were present during kidney development and contributed to formation of the proximal tubule and collecting duct structures in mature mouse kidneys. In three-dimensional culture, single Lrig1+ cells demonstrated long-lasting propagation and differentiated into the proximal tubule and collecting duct lineages. These Lrig1+ proximal tubule cells highly expressed progenitor-like and quiescence-related genes, giving rise to a novel cluster of cells with regenerative potential in adult kidneys. Moreover, these long-lived Lrig1+ cells expanded and repaired damaged proximal tubule in response to three types of AKIs in mice.ConclusionsThese findings highlight the critical role of Lrig1+ cells in kidney regeneration. Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology.
Author(s)
Lee, YuraKim, Kwang H.Park, JihwanKang, Hyun MiKim, Sung-HeeJeong, HaengduengLee, BuhyunLee, NakyumCho, YejinKim, Gyeong DaeYu, SeyoungGee, Heon YungBok, JinwoongHamilton, Maxwell S.Gewin, LeslieAronow, Bruce J.Lim, Kyung-MinCoffey, Robert J.Nam, Ki Taek
Issued Date
2024-12
Type
Article
DOI
10.1681/ASN.0000000000000462
URI
https://scholar.gist.ac.kr/handle/local/9200
Publisher
Lippincott Williams & Wilkins Ltd.
Citation
Journal of the American Society of Nephrology : JASN, v.35, no.12, pp.1702 - 1714
ISSN
1046-6673
Appears in Collections:
Department of Life Sciences > 1. Journal Articles
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