MEMO1 Is Required for Ameloblast Maturation and Functional Enamel Formation.

amelogenesis amelogenesis imperfecta cell polarity cytoskeleton mineralization tooth

Journal

Journal of dental research
ISSN: 1544-0591
Titre abrégé: J Dent Res
Pays: United States
ID NLM: 0354343

Informations de publication

Date de publication:
Oct 2023
Historique:
pubmed: 21 7 2023
medline: 21 7 2023
entrez: 21 7 2023
Statut: ppublish

Résumé

Coordinated mineralization of soft tissue is central to organismal form and function, while dysregulated mineralization underlies several human pathologies. Oral epithelial-derived ameloblasts are polarized, secretory cells responsible for generating enamel, the most mineralized substance in the human body. Defects in ameloblast development result in enamel anomalies, including amelogenesis imperfecta. Identifying proteins critical in ameloblast development can provide insight into specific pathologies associated with enamel-related disorders or, more broadly, mechanisms of mineralization. Previous studies identified a role for MEMO1 in bone mineralization; however, whether MEMO1 functions in the generation of additional mineralized structures remains unknown. Here, we identify a critical role for MEMO1 in enamel mineralization. First, we show that

Identifiants

pubmed: 37475472
doi: 10.1177/00220345231185758
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1261-1271

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

M Kiel (M)

Iowa Institute for Oral Health Research, University of Iowa, College of Dentistry & Dental Clinics, Iowa City, IA, USA.
Department of Anatomy and Cell Biology, University of Iowa, Carver College of Medicine, Iowa City, IA, USA.

S Wuebker (S)

Iowa Institute for Oral Health Research, University of Iowa, College of Dentistry & Dental Clinics, Iowa City, IA, USA.
Department of Anatomy and Cell Biology, University of Iowa, Carver College of Medicine, Iowa City, IA, USA.

M T Remy (MT)

Iowa Institute for Oral Health Research, University of Iowa, College of Dentistry & Dental Clinics, Iowa City, IA, USA.
Roy J. Carver Department of Biomedical Engineering, College of Engineering, University of Iowa, Iowa City, IA, USA.

K A Riemondy (KA)

RNA Bioscience Initiative, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

F Smith (F)

Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

C M Carey (CM)

Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.

T Williams (T)

Department of Craniofacial Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Department of Cell and Developmental Biology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Department of Pediatrics, University of Colorado Anschutz Medical Campus, Children's Hospital Colorado, Aurora, CO, USA.

E Van Otterloo (E)

Iowa Institute for Oral Health Research, University of Iowa, College of Dentistry & Dental Clinics, Iowa City, IA, USA.
Department of Anatomy and Cell Biology, University of Iowa, Carver College of Medicine, Iowa City, IA, USA.
Department of Periodontics, University of Iowa, College of Dentistry & Dental Clinics, Iowa City, IA, USA.
The University of Iowa Craniofacial Anomalies Research Center, University of Iowa, Iowa City, IA, USA.

Classifications MeSH