A role for Dynlt3 in melanosome movement, distribution, acidity and transfer.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
26 03 2021
Historique:
received: 04 04 2020
accepted: 25 02 2021
entrez: 27 3 2021
pubmed: 28 3 2021
medline: 6 8 2021
Statut: epublish

Résumé

Skin pigmentation is dependent on cellular processes including melanosome biogenesis, transport, maturation and transfer to keratinocytes. However, how the cells finely control these processes in space and time to ensure proper pigmentation remains unclear. Here, we show that a component of the cytoplasmic dynein complex, Dynlt3, is required for efficient melanosome transport, acidity and transfer. In Mus musculus melanocytes with decreased levels of Dynlt3, pigmented melanosomes undergo a more directional motion, leading to their peripheral location in the cell. Stage IV melanosomes are more acidic, but still heavily pigmented, resulting in a less efficient melanosome transfer. Finally, the level of Dynlt3 is dependent on β-catenin activity, revealing a function of the Wnt/β-catenin signalling pathway during melanocyte and skin pigmentation, by coupling the transport, positioning and acidity of melanosomes required for their transfer.

Identifiants

pubmed: 33772156
doi: 10.1038/s42003-021-01917-5
pii: 10.1038/s42003-021-01917-5
pmc: PMC7997999
doi:

Substances chimiques

DYNLT3 protein, mouse EC 3.6.1.-
Dyneins EC 3.6.4.2

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

423

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Auteurs

Zackie Aktary (Z)

Normal and Pathological Development of Melanocytes, Institut Curie, CNRS UMR3347, Inserm U1021, Université PSL, Orsay, France.
Signalisation Radiobiologie et Cancer, CNRS UMR3347, Inserm U1021, Université Paris-Saclay, Orsay, France.
Equipe Labellisée - Ligue Contre le Cancer, Orsay, France.

Alejandro Conde-Perez (A)

Normal and Pathological Development of Melanocytes, Institut Curie, CNRS UMR3347, Inserm U1021, Université PSL, Orsay, France.
Signalisation Radiobiologie et Cancer, CNRS UMR3347, Inserm U1021, Université Paris-Saclay, Orsay, France.
Equipe Labellisée - Ligue Contre le Cancer, Orsay, France.

Florian Rambow (F)

Normal and Pathological Development of Melanocytes, Institut Curie, CNRS UMR3347, Inserm U1021, Université PSL, Orsay, France.
Signalisation Radiobiologie et Cancer, CNRS UMR3347, Inserm U1021, Université Paris-Saclay, Orsay, France.
Equipe Labellisée - Ligue Contre le Cancer, Orsay, France.

Mathilde Di Marco (M)

CNRS UMR144, Structure and Membrane Compartments, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.

François Amblard (F)

Laboratoire Physico-Chimie Curie, Institut Curie, PSL Research University - Sorbonne Universités, UPMC-CNRS, Paris, France.
Departments of Bioengineering and Physics, Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan National Institute of Science and Technology, Ulsan, South Korea.

Ilse Hurbain (I)

CNRS UMR144, Structure and Membrane Compartments, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.
CNRS UMR144, Cell and Tissue Imaging Facility, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.

Graça Raposo (G)

CNRS UMR144, Structure and Membrane Compartments, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.
CNRS UMR144, Cell and Tissue Imaging Facility, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.

Cédric Delevoye (C)

CNRS UMR144, Structure and Membrane Compartments, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.
CNRS UMR144, Cell and Tissue Imaging Facility, Institut Curie, Centre National de la Recherche Scientifique, Paris Sciences & Lettres Research University, Paris, France.

Sylvie Coscoy (S)

Laboratoire Physico-Chimie Curie, Institut Curie, PSL Research University - Sorbonne Universités, UPMC-CNRS, Paris, France.

Lionel Larue (L)

Normal and Pathological Development of Melanocytes, Institut Curie, CNRS UMR3347, Inserm U1021, Université PSL, Orsay, France. lionel.larue@curie.fr.
Signalisation Radiobiologie et Cancer, CNRS UMR3347, Inserm U1021, Université Paris-Saclay, Orsay, France. lionel.larue@curie.fr.
Equipe Labellisée - Ligue Contre le Cancer, Orsay, France. lionel.larue@curie.fr.

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Classifications MeSH