Insulin Receptor deletion in S100a4-lineage cells accelerates age-related bone loss.

Aging Bone Bone homeostasis Insulin receptor S100a4

Journal

Bone reports
ISSN: 2352-1872
Titre abrégé: Bone Rep
Pays: United States
ID NLM: 101646176

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 04 10 2018
revised: 28 01 2019
accepted: 01 02 2019
entrez: 27 2 2019
pubmed: 26 2 2019
medline: 26 2 2019
Statut: epublish

Résumé

Type I and Type II Diabetes dramatically impair skeletal health. Altered Insulin Receptor (IR) signaling is a common feature of both diseases, and insulin has potent bone anabolic functions. Several previous studies have demonstrated that loss of IR in bone cells results in disrupted bone homeostasis during early post-natal growth. Here we have deleted IR in S100a4-lineage cells (IRcKO

Identifiants

pubmed: 30805422
doi: 10.1016/j.bonr.2019.100197
pii: S2352-1872(19)30003-8
pii: 100197
pmc: PMC6374520
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100197

Subventions

Organisme : NIAMS NIH HHS
ID : K01 AR068386
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR069655
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR073169
Pays : United States

Commentaires et corrections

Type : ErratumIn

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Auteurs

Valentina Studentsova (V)

Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY 14642, United States of America.

Emma Knapp (E)

Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY 14642, United States of America.

Alayna E Loiselle (AE)

Center for Musculoskeletal Research, University of Rochester Medical Center, Rochester, NY 14642, United States of America.

Classifications MeSH