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Vasculature-driven stem cell population coordinates tissue scaling in dynamic organs

Authors :
50804382
20778279
60546993
40397576
Ichijo, Ryo
Kabata, Mio
Kidoya, Hiroyasu
Muramatsu, Fumitaka
Ishibashi, Riki
Abe, Kota
Tsutsui, Ko
Kubo, Hirokazu
Iizuka, Yui
Kitano, Satsuki
Miyachi, Hitoshi
Kubota, Yoshiaki
Fujiwara, Hironobu
Sada, Aiko
Yamamoto, Takuya
Toyoshima, Fumiko
50804382
20778279
60546993
40397576
Ichijo, Ryo
Kabata, Mio
Kidoya, Hiroyasu
Muramatsu, Fumitaka
Ishibashi, Riki
Abe, Kota
Tsutsui, Ko
Kubo, Hirokazu
Iizuka, Yui
Kitano, Satsuki
Miyachi, Hitoshi
Kubota, Yoshiaki
Fujiwara, Hironobu
Sada, Aiko
Yamamoto, Takuya
Toyoshima, Fumiko
Publication Year :
2021

Abstract

Stem cell (SC) proliferation and differentiation organize tissue homeostasis. However, how SCs regulate coordinate tissue scaling in dynamic organs remain unknown. Here, we delineate SC regulations in dynamic skin. We found that interfollicular epidermal SCs (IFESCs) shape basal epidermal proliferating clusters (EPCs) in expanding abdominal epidermis of pregnant mice and proliferating plantar epidermis. EPCs consist of IFESC-derived Tbx3⁺–basal cells (Tbx3⁺-BCs) and their neighboring cells where Adam8–extracellular signal–regulated kinase signaling is activated. Clonal lineage tracing revealed that Tbx3⁺-BC clones emerge in the abdominal epidermis during pregnancy, followed by differentiation after parturition. In the plantar epidermis, Tbx3⁺-BCs are sustained as long-lived SCs to maintain EPCs invariably. We showed that Tbx3⁺-BCs are vasculature-dependent IFESCs and identified mechanical stretch as an external cue for the vasculature-driven EPC formation. Our results uncover vasculature-mediated IFESC regulations, which explain how the epidermis adjusts its size in orchestration with dermal constituents in dynamic skin.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1458633622
Document Type :
Electronic Resource