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The developmental and evolutionary origins of cellular pluripotency in the vertebrate neural crest

Producción científica: Review articlerevisión exhaustiva

18 Citas (Scopus)

Resumen

Neural crest cells are central to vertebrate development and evolution, endowing vertebrates with a “new head” that resulted in morphological, physiological, and behavioral features that allowed vertebrates to become active predators. One remarkable feature of neural crest cells is their multi-germ layer potential that allows for the formation of both ectodermal (pigmentation, peripheral glia, sensory neurons) and mesenchymal (connective tissue, cartilage/bone, dermis) cell types. Understanding the cellular and evolutionary origins of this broad cellular potential in the neural crest has been a long-standing focus for developmental biologists. Here, we review recent work that has demonstrated that neural crest cells share key features with pluripotent blastula stem cells, including expression of the Yamanaka stem cell factors (Oct3/4, Klf4, Sox2, c-Myc). These shared features suggest that pluripotency is either retained in the neural crest from blastula stages or subsequently reactivated as the neural crest forms. We highlight the cellular and molecular parallels between blastula stem cells and neural crest cells and discuss the work that has led to current models for the cellular origins of broad potential in the crest. Finally, we explore how these themes can provide new insights into how and when neural crest cells and pluripotency evolved in vertebrates and the evolutionary relationship between these populations.

Idioma originalEnglish
Páginas (desde-hasta)36-44
Número de páginas9
PublicaciónSeminars in Cell and Developmental Biology
Volumen138
DOI
EstadoPublished - mar 30 2023

Nota bibliográfica

Publisher Copyright:
© 2022

Financiación

The authors acknowledge funding support from the NIH ( 1F32DE029113-ENS and R01GM116538-CL ), the National Science Foundation ( 1764421, CL ), and Simons Foundation ( SFARI 597491-RWC, CL ). JRY is a Walder Foundation Fellow of the Life Sciences Research Foundation.

FinanciadoresNúmero del financiador
Life Sciences Research Foundation
U.S. Department of Energy Chinese Academy of Sciences Guangzhou Municipal Science and Technology Project Oak Ridge National Laboratory Extreme Science and Engineering Discovery Environment National Science Foundation National Energy Research Scientific Computing Center National Natural Science Foundation of China1764421
National Institutes of Health (NIH)R01GM116538-CL
Simons FoundationSFARI 597491-RWC

    ASJC Scopus subject areas

    • Developmental Biology
    • Cell Biology

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