| Literature DB >> 33181078 |
Stacey M Frumm1, Shengyang Kevin Yu1, Joseph Chang1, Jordan A Artichoker2, Sonia M Scaria1, Katharine P Lee1, Lauren E Byrnes3, Julie B Sneddon4, Aaron D Tward5.
Abstract
The tympanic membrane (TM) is critical for hearing and requires continuous clearing of cellular debris, but little is known about homeostatic mechanisms in the TM epidermis. Using single-cell RNA sequencing, lineage tracing, whole-organ explant, and live-cell imaging, we show that homeostatic TM epidermis is distinct from other epidermal sites and has discrete proliferative zones with a three-dimensional hierarchy of multiple keratinocyte populations. TM stem cells reside in a discrete location of the superior TM and generate long-lived clones and committed progenitors (CPs). CP clones exhibit lateral migration, and their proliferative capacity is supported by Pdgfra+ fibroblasts, generating migratory but non-proliferative progeny. Single-cell sequencing of the human TM revealed similar cell types and transcriptional programming. Thus, during homeostasis, TM keratinocytes transit through a proliferative CP state and exhibit directional lateral migration. This work forms a foundation for understanding TM disorders and modeling keratinocyte biology.Entities:
Keywords: committed progenitor; epidermis; keratinocyte; malleus; migration; stem cell; tympanic membrane
Mesh:
Year: 2020 PMID: 33181078 PMCID: PMC8962966 DOI: 10.1016/j.stem.2020.10.006
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269