The Actin-Based Motor Myosin Vb Is Crucial to Maintain Epidermal Barrier Integrity.
Actin Cytoskeleton
/ metabolism
Actins
/ metabolism
Cells, Cultured
Claudin-1
/ metabolism
Epidermis
/ metabolism
Humans
Intercellular Signaling Peptides and Proteins
/ metabolism
Keratinocytes
/ metabolism
Myosin Heavy Chains
/ genetics
Myosin Type V
/ genetics
Protein Binding
Protein Transport
RNA, Small Interfering
/ genetics
Tight Junctions
/ metabolism
rab GTP-Binding Proteins
/ metabolism
Journal
The Journal of investigative dermatology
ISSN: 1523-1747
Titre abrégé: J Invest Dermatol
Pays: United States
ID NLM: 0426720
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
04
10
2018
revised:
05
12
2018
accepted:
12
12
2018
pubmed:
21
1
2019
medline:
28
5
2020
entrez:
21
1
2019
Statut:
ppublish
Résumé
Myosin Vb (Myo5b) is an unconventional myosin involved in the actin-dependent transport and tethering of intracellular organelles. In the epidermis, granular keratinocytes accumulate cytoplasmic lamellar bodies (LBs), secretory vesicles released at the junction with the stratum corneum that participate actively in the maintenance of the epidermal barrier. We have previously demonstrated that LB biogenesis is controlled by the Rab11a guanosine triphosphate hydrolase, known for its ability to recruit the Myo5b motor. In order to better characterize the molecular pathway that controls LB trafficking, we analyzed the role of F-actin and Myo5b in the epidermis. We demonstrated that LB distribution in granular keratinocytes was dependent on a dynamic F-actin cytoskeleton. Myo5b was shown to be highly expressed in granular keratinocytes and associated with corneodesmosin-loaded LB. In reconstructed human epidermis, Myo5b silencing led to epidermal barrier defects associated with structural alterations of the stratum corneum and a reduced pool of LB showing signs of disordered maturation. Myo5b depletion also disturbed the expression and distribution of both LB cargoes and junctional components, such as claudin-1, which demonstrates its action on both LB trafficking and junctional complex composition. Together, our data reveal the essential role of Myo5b in maintaining the epidermal barrier integrity.
Identifiants
pubmed: 30660668
pii: S0022-202X(19)30014-4
doi: 10.1016/j.jid.2018.12.021
pii:
doi:
Substances chimiques
Actins
0
CDSN protein, human
0
Claudin-1
0
Intercellular Signaling Peptides and Proteins
0
MYO5B protein, human
0
RNA, Small Interfering
0
Myosin Type V
EC 3.6.1.-
rab11 protein
EC 3.6.1.-
Myosin Heavy Chains
EC 3.6.4.1
rab GTP-Binding Proteins
EC 3.6.5.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1430-1438Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.