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Intracellular pH dynamics regulates intestinal stem cell lineage specification.
Liu, Yi; Reyes, Efren; Castillo-Azofeifa, David; Klein, Ophir D; Nystul, Todd; Barber, Diane L.
Afiliação
  • Liu Y; Department of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA, 94143, USA.
  • Reyes E; Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA, 94143, USA.
  • Castillo-Azofeifa D; Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA, 94143, USA.
  • Klein OD; Immunology Discovery, Genentech, Inc., South San Francisco, CA, 94080, USA.
  • Nystul T; Program in Craniofacial Biology and Department of Orofacial Sciences, University of California San Francisco, San Francisco, CA, 94143, USA.
  • Barber DL; Departments of Anatomy, University of California San Francisco, San Francisco, CA, 94143, USA. todd.nystul@ucsf.edu.
Nat Commun ; 14(1): 3745, 2023 06 23.
Article em En | MEDLINE | ID: mdl-37353491
ABSTRACT
Intracellular pH dynamics is increasingly recognized to regulate myriad cell behaviors. We report a finding that intracellular pH dynamics also regulates adult stem cell lineage specification. We identify an intracellular pH gradient in mouse small intestinal crypts, lowest in crypt stem cells and increasing along the crypt column. Disrupting this gradient by inhibiting H+ efflux by Na+/H+ exchanger 1 abolishes crypt budding and blocks differentiation of Paneth cells, which are rescued with exogenous WNT. Using single-cell RNA sequencing and lineage tracing we demonstrate that intracellular pH dynamics acts downstream of ATOH1, with increased pH promoting differentiation toward the secretory lineage. Our findings indicate that an increase in pH is required for the lineage specification that contributes to crypt maintenance, establishing a role for intracellular pH dynamics in cell fate decisions within an adult stem cell lineage.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Intestinos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco / Intestinos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos