Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis.

Koren, Elle; Feldman, Alona; Yusupova, Marianna; Kadosh, Avihay; Sedov, Egor; Ankawa, Roi; Yosefzon, Yahav; Nasser, Waseem et al. · Nat Commun · 2022

basic_science · Level V

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Abstract

The presence of distinct stem cells that maintain the interfollicular epidermis is highly debated. Here, we report a population of keratinocytes, marked by Thy1, in the basal layer of the interfollicular epidermis. We find that epidermal cells expressing differential levels of Thy1 display distinct transcriptional signatures. Thy1<sup>+</sup> keratinocytes do not express T cell markers, express a unique transcriptional profile, cycle significantly slower than basal epidermal progenitors and display significant expansion potential in vitro. Multicolor lineage tracing analyses and mathematical modeling reveal that Thy1<sup>+</sup> basal keratinocytes do not compete neutrally alike interfollicular progenitors and contribute long-term to both epidermal replenishment and wound repair. Importantly, ablation of Thy1<sup>+</sup> cells strongly impairs these processes, thus indicating the non-redundant function of Thy1<sup>+</sup> stem cells in the epidermis. Collectively, these results reveal a distinct stem cell population that plays a critical role in epidermal homeostasis and repair.

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