Functions of LKB1 in neural crest development: The story unfolds.


Journal

Developmental dynamics : an official publication of the American Association of Anatomists
ISSN: 1097-0177
Titre abrégé: Dev Dyn
Pays: United States
ID NLM: 9201927

Informations de publication

Date de publication:
08 2023
Historique:
revised: 20 02 2023
received: 08 09 2022
accepted: 20 02 2023
medline: 8 8 2023
pubmed: 8 3 2023
entrez: 7 3 2023
Statut: ppublish

Résumé

Neural crest cells (NCCs) are highly motile, multipotent, embryonic cells that delaminate from the dorsal edges of the neural tube. NCCs follow stereotypical long-range migratory pathways to reach target organs during development, where they give rise to multiple derivatives. The identification of reservoirs of neural crest stem cells that persist to adulthood has recently aroused renewed interest in the biology of NCCs. In this context, several recent studies have demonstrated the essential role of the metabolic kinase LKB1 in NCC establishment. This review surveys how LKB1 governs the formation and maintenance of several neural crest derivatives, including facial bones, melanocytes, Schwann cells, and the enteric nervous system. We also detail the underlying molecular mechanisms that involve downstream effectors of LKB1, in particular the contribution of the AMPK-mTOR signaling pathway to both polarity and metabolic processes. Collectively, these recent discoveries open promising perspectives for new therapeutic applications for the treatment of neural crest disorders.

Identifiants

pubmed: 36880501
doi: 10.1002/dvdy.581
doi:

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1077-1095

Informations de copyright

© 2023 The Authors. Developmental Dynamics published by Wiley Periodicals LLC on behalf of American Association for Anatomy.

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Auteurs

Chantal Thibert (C)

Univ. Grenoble Alpes, INSERM 1209, CNRS 5309, Institute for Advanced Biosciences, Grenoble, France.

Anthony Lucas (A)

Univ. Grenoble Alpes, INSERM 1209, CNRS 5309, Institute for Advanced Biosciences, Grenoble, France.

Marc Billaud (M)

Cell death and Childhood Cancers team, Cancer Research Center of Lyon, INSERM U1052, CNRS UMR5286, University of Lyon, Centre Léon Bérard, Lyon, France.

Sakina Torch (S)

Univ. Grenoble Alpes, INSERM 1209, CNRS 5309, Institute for Advanced Biosciences, Grenoble, France.

Marie Mével-Aliset (M)

Univ. Grenoble Alpes, INSERM 1209, CNRS 5309, Institute for Advanced Biosciences, Grenoble, France.

Jordan Allard (J)

Univ. Grenoble Alpes, INSERM 1209, CNRS 5309, Institute for Advanced Biosciences, Grenoble, France.

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Classifications MeSH