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

Author(s)
Aktary, ZackieConde-Perez, AlejandroRambow, FlorianDi Marco, MathildeAmblard, FrancoisHurbain, IlseRaposo, GracaDelevoye, CedricCoscoy, SylvieLarue, Lionel
Issued Date
2021-03
DOI
10.1038/s42003-021-01917-5
URI
https://scholarworks.unist.ac.kr/handle/201301/52818
Fulltext
https://www.nature.com/articles/s42003-021-01917-5
Citation
COMMUNICATIONS BIOLOGY, v.4, no.1, pp.423
Abstract
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 beta -catenin activity, revealing a function of the Wnt/beta -catenin signalling pathway during melanocyte and skin pigmentation, by coupling the transport, positioning and acidity of melanosomes required for their transfer. Aktary et al. identify novel roles for the dynein light chain Dynlt3 in melanosome transport, maturation, and transfer to keratinocytes. They also find that the Wnt/beta catenin signalling pathway controls Dynlt3 levels and thus also contributes to the regulation of melanocyte transport and skin pigmentation.
Publisher
NATURE RESEARCH
ISSN
2399-3642

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