Membrane progesterone receptor α (mPRα/PAQR7) promotes migration, proliferation and BDNF release in human Schwann cell-like differentiated adipose stem cells.
Adipocytes
/ cytology
Brain-Derived Neurotrophic Factor
/ metabolism
Cell Differentiation
Cell Movement
Cell Proliferation
Cells, Cultured
Gene Expression Regulation
Humans
Primary Cell Culture
Receptors, G-Protein-Coupled
/ genetics
Receptors, Progesterone
/ genetics
Regeneration
Schwann Cells
/ cytology
Signal Transduction
Stem Cells
/ cytology
Up-Regulation
Adipose stem cells
Brain-derived neurotrophic factor
Cell migration
Cell proliferation
Membrane progesterone receptor α
Peripheral nerve regeneration
Journal
Molecular and cellular endocrinology
ISSN: 1872-8057
Titre abrégé: Mol Cell Endocrinol
Pays: Ireland
ID NLM: 7500844
Informations de publication
Date de publication:
01 07 2021
01 07 2021
Historique:
received:
19
03
2021
revised:
20
04
2021
accepted:
21
04
2021
pubmed:
1
5
2021
medline:
15
12
2021
entrez:
30
4
2021
Statut:
ppublish
Résumé
Membrane progesterone receptors (mPRs) were recently found to be present and active in Schwann cells, where they have a potentially pro-regenerative activity. In this study, we investigated the role of mPRs in human adipose stem cells (ASC) differentiated into Schwann cell-like cells (SCL-ASC), which represent a promising alternative to Schwann cells for peripheral nerve regeneration. Our findings show that mPRs are present both in undifferentiated and differentiated ASC, and that the differentiation protocol upregulates mPR expression. Activation of mPRα promoted cell migration and differentiation in SCL-ASC, alongside with changes in cell morphology and mPRα localization. Moreover, it increased the expression and release of BDNF, a neurotrophin with pro-regenerative activity. Further analysis showed that Src and PI3K-Akt signaling pathways are involved in mPRα activity in SCL-ASC. These findings suggest that mPRα could play a pro-regenerative role in SCL-ASC and may be a promising target for the promotion of peripheral nerve regeneration.
Identifiants
pubmed: 33930460
pii: S0303-7207(21)00142-8
doi: 10.1016/j.mce.2021.111298
pii:
doi:
Substances chimiques
Brain-Derived Neurotrophic Factor
0
Receptors, G-Protein-Coupled
0
Receptors, Progesterone
0
membrane progestin receptor alpha, human
0
BDNF protein, human
7171WSG8A2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
111298Informations de copyright
Copyright © 2021 Elsevier B.V. All rights reserved.