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A transit-amplifying progenitor with biphasic behavior contributes to epidermal renewal.
Ghuwalewala, Sangeeta; Jiang, Kevin; Ragi, Sara; Shalloway, David; Tumbar, Tudorita.
Affiliation
  • Ghuwalewala S; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
  • Jiang K; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
  • Ragi S; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
  • Shalloway D; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
  • Tumbar T; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14850, USA.
Development ; 151(12)2024 Jun 15.
Article in En | MEDLINE | ID: mdl-38934416
ABSTRACT
Transit-amplifying (TA) cells are progenitors that undergo an amplification phase followed by transition into an extinction phase. A long postulated epidermal TA progenitor with biphasic behavior has not yet been experimentally observed in vivo. Here, we identify such a TA population using clonal analysis of Aspm-CreER genetic cell-marking in mice, which uncovers contribution to both homeostasis and injury repair of adult skin. This TA population is more frequently dividing than a Dlx1-CreER-marked long-term self-renewing (e.g. stem cell) population. Newly developed generalized birth-death modeling of long-term lineage tracing data shows that both TA progenitors and stem cells display neutral competition, but only the stem cells display neutral drift. The quantitative evolution of a nascent TA cell and its direct descendants shows that TA progenitors indeed amplify the basal layer before transition and that the homeostatic TA population is mostly in extinction phase. This model will be broadly useful for analyzing progenitors whose behavior changes with their clone age. This work identifies a long-missing class of non-self-renewing biphasic epidermal TA progenitors and has broad implications for understanding tissue renewal mechanisms.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Epidermis / Epidermal Cells Limits: Animals Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stem Cells / Epidermis / Epidermal Cells Limits: Animals Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2024 Type: Article Affiliation country: United States