Extracellular vesicles released by keratinocytes regulate melanosome maturation, melanocyte dendricity and pigment transfer
- Others:
- Biologie Cellulaire et Cancer ; Institut Curie [Paris]-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
- Université Paris sciences et lettres (PSL)
- Institut de Biologie Valrose (IBV) ; Université Nice Sophia Antipolis (1965 - 2019) (UNS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
- BioImaging Cell and Tissue Core Facility (PICT-IBiSA) ; Institut Curie [Paris]
- Institut Curie [Paris]
- Fondation pour la Recherche Médicale (FRM EQU201903007827)
- European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie (Grant agreement No 847718)
- Fondation pour la Recherche Médicale (FRM SPF201809006932)
- Institut Curie EuReCa PhD Programme
Description
Extracellular vesicles (EVs) facilitate the transfer of proteins, lipids and genetic material molecules between cells, and are recognized as an additional mechanism for sustaining intercellular communication. In the epidermis, the communication between melanocytes and keratinocytes is tightly regulated to warrant skin pigmentation. Melanocytes synthetize the melanin pigment in melanosomes that are transported along the dendrites prior to the transfer of melanin pigment to keratinocytes. EVs secreted by keratinocytes modulate pigmentation in melanocytes (Lo Cicero et al., Nat. Comm. 2015). However, whether EVs secreted by keratinocytes contribute to additional processes essential for melanocyte functions remains elusive. Here we show that keratinocyte EVs enhance the ability of melanocytes to generate dendrites, mature melanosomes and their efficient transfer. Further, keratinocyte EVs carrying Rac1 induce important morphological changes, promote dendrite outgrowth, and potentiate melanin transfer to keratinocytes. Hence, in addition to modulate pigmentation, keratinocytes exploit EVs to control melanocyte plasticity and transfer capacity. These data demonstrate that keratinocyte-derived EVs, by regulating melanocyte functions, are major contributors of cutaneous pigmentation and expand our understanding of the mechanism underlying skin pigmentation via a paracrine EV-mediated communication.
Abstract
manuscript déposé dans bioRxiv
Additional details
- URL
- https://hal.science/hal-04333257
- URN
- urn:oai:HAL:hal-04333257v1
- Origin repository
- UNICA