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A transitory signaling center controls timing of primordial germ cell differentiation.
Banisch, Torsten U; Slaidina, Maija; Gupta, Selena; Ho, Megan; Gilboa, Lilach; Lehmann, Ruth.
Afiliação
  • Banisch TU; Department of Cell Biology, Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA. Electronic address: torsten.banisch@nyumc.org.
  • Slaidina M; Department of Cell Biology, Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA.
  • Gupta S; Department of Cell Biology, Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA.
  • Ho M; Department of Cell Biology, Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA.
  • Gilboa L; Department of Biological Regulation, Weizmann Institute of Science, Rehovot 7610001, Israel.
  • Lehmann R; Department of Cell Biology, Howard Hughes Medical Institute, Skirball Institute of Biomolecular Medicine, NYU School of Medicine, New York, NY 10016, USA. Electronic address: lehmann@wi.mit.edu.
Dev Cell ; 56(12): 1742-1755.e4, 2021 06 21.
Article em En | MEDLINE | ID: mdl-34081907
ABSTRACT
Organogenesis requires exquisite spatiotemporal coordination of cell morphogenesis, migration, proliferation, and differentiation of multiple cell types. For gonads, this involves complex interactions between somatic and germline tissues. During Drosophila ovary morphogenesis, primordial germ cells (PGCs) either are sequestered in stem cell niches and are maintained in an undifferentiated germline stem cell state or transition directly toward differentiation. Here, we identify a mechanism that links hormonal triggers of somatic tissue morphogenesis with PGC differentiation. An early ecdysone pulse initiates somatic swarm cell (SwC) migration, positioning these cells close to PGCs. A second hormone peak activates Torso-like signal in SwCs, which stimulates the Torso receptor tyrosine kinase (RTK) signaling pathway in PGCs promoting their differentiation by de-repression of the differentiation gene, bag of marbles. Thus, systemic temporal cues generate a transitory signaling center that coordinates ovarian morphogenesis with stem cell self-renewal and differentiation programs, highlighting a more general role for such centers in reproductive and developmental biology.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ovário / Diferenciação Celular / Receptores Proteína Tirosina Quinases / Proteínas de Drosophila / Células Germinativas / Morfogênese Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ovário / Diferenciação Celular / Receptores Proteína Tirosina Quinases / Proteínas de Drosophila / Células Germinativas / Morfogênese Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article