Antagonistic Roles of Tau and MAP6 in Regulating Neuronal Development.

Axon growth Growth cone turning MAP6 Microtubule Neuronal migration Tau

Journal

Journal of cell science
ISSN: 1477-9137
Titre abrégé: J Cell Sci
Pays: England
ID NLM: 0052457

Informations de publication

Date de publication:
11 Sep 2024
Historique:
received: 21 02 2024
accepted: 20 08 2024
medline: 11 9 2024
pubmed: 11 9 2024
entrez: 11 9 2024
Statut: aheadofprint

Résumé

Association of tau with microtubules causes them to be labile while association of MAP6 with microtubules causes them to be stable. As axons differentiate and grow, tau and MAP6 segregate from one another on individual microtubules, resulting in the formation of stable and labile domains. The functional significance of the yin/yang relationship between tau and MAP6 remains speculative, with one idea being that such a relationship assists in balancing morphological stability with plasticity. Here, using primary rodent neuronal cultures, we show that tau depletion has opposite effects compared to MAP6 depletion on the rate of neuronal development, the efficiency of growth cone turning, and the number of neuronal processes and axonal branches. Opposite effects to those of tau depletion were also observed on the rate of neuronal migration, in an in vivo assay, when MAP6 was depleted. When tau and MAP6 were together depleted from neuronal cultures, the morphological phenotypes negated one another. Although tau and MAP6 are multifunctional proteins, our results suggest that the observed effects on neuronal development are likely due to their opposite roles in regulating microtubule stability.

Identifiants

pubmed: 39257379
pii: 362002
doi: 10.1242/jcs.261966
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Lisa Dean Moseley Foundation Reseach Grant
Organisme : National Institutes of Health/ National Institute of Neurological Disorders and Stroke
Organisme : CURE program via Drexel University College of Medicine
Organisme : National Institutes of Health/ National Institute on Aging
Organisme : National Institutes of Health/ National Institute of Neurological Disorders and Stroke
Organisme : U.S. Department of Defense

Informations de copyright

© 2024. Published by The Company of Biologists Ltd.

Auteurs

Xiaohuan Sun (X)

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Wenqian Yu (W)

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Peter W Baas (PW)

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Kazuhito Toyooka (K)

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Liang Qiang (L)

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA 19129, USA.

Classifications MeSH