Phospholipase C-β1 interacts with cyclin E in adipose- derived stem cells osteogenic differentiation.


Journal

Advances in biological regulation
ISSN: 2212-4934
Titre abrégé: Adv Biol Regul
Pays: England
ID NLM: 101572336

Informations de publication

Date de publication:
01 2019
Historique:
received: 22 10 2018
revised: 29 10 2018
accepted: 04 11 2018
pubmed: 14 11 2018
medline: 5 3 2020
entrez: 14 11 2018
Statut: ppublish

Résumé

Adipose-derived stem cells (ADSCs) are multipotent mesenchymal stem cells that have the ability to differentiate into several cell types, including chondrocytes, osteoblasts, adipocytes, and neural cells. Given their easy accessibility and abundance, they became an attractive source of mesenchymal stem cells, as well as candidates for developing new treatments for reconstructive medicine and tissue engineering. Our study identifies a new signaling pathway that promotes ADSCs osteogenic differentiation and links the lipid signaling enzyme phospholipase C (PLC)-β1 to the expression of the cell cycle protein cyclin E. During osteogenic differentiation, PLC-β1 expression varies concomitantly with cyclin E expression and the two proteins interact. These findings contribute to clarify the pathways involved in osteogenic differentiation and provide evidence to develop therapeutic strategies for bone regeneration.

Identifiants

pubmed: 30420274
pii: S2212-4926(18)30152-0
doi: 10.1016/j.jbior.2018.11.001
pii:
doi:

Substances chimiques

CCNE1 protein, human 0
Cyclin E 0
Oncogene Proteins 0
PLCB1 protein, human EC 3.1.4.11
Phospholipase C beta EC 3.1.4.11

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Informations de copyright

Copyright © 2018. Published by Elsevier Ltd.

Auteurs

Giulia Ramazzotti (G)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Roberta Fiume (R)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Francesca Chiarini (F)

Institute of Molecular Genetics - Bologna Unit, c/o Istituto Ortopedico Rizzoli, via di Barbiano 1-10, 40138, Bologna, Italy.

Gabriele Campana (G)

Department of Pharmacy and Biotechnology, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Stefano Ratti (S)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Anna Maria Billi (AM)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Lucia Manzoli (L)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Matilde Y Follo (MY)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Pann-Gill Suh (PG)

Ulsan National Institute of Science and Technology (UNIST), Ulsan Metropolitan City, Republic of Korea.

James McCubrey (J)

East Carolina University, Greenville, NC, USA.

Lucio Cocco (L)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy.

Irene Faenza (I)

Section of Human Anatomy, Department of Biomedical and Neuromotor Sciences, University of Bologna, via Irnerio 48, 40126, Bologna, Italy. Electronic address: Irene.faenza2@unibo.it.

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Classifications MeSH