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miR‑203‑3p participates in the suppression of diabetes‑associated osteogenesis in the jaw bone through targeting Smad1.
- Source :
-
International journal of molecular medicine [Int J Mol Med] 2018 Mar; Vol. 41 (3), pp. 1595-1607. Date of Electronic Publication: 2018 Jan 09. - Publication Year :
- 2018
-
Abstract
- Certain microRNAs (miRs) have important roles in the maintenance of bone development and metabolism, and a variety of miRs are known to be deregulated in diabetes. The present study investigated the role of miR‑203‑3p in the regulation of bone loss by assessing jaw bones of a rat model of type 2 diabetes. The results indicated that miR‑203‑3p inhibited osteogenesis in the jaws of diabetic rats and in rat bone marrow mesenchymal stem cells cultured in high‑glucose medium. A luciferase re-porter assay was used to verify the bioinformatics prediction that miR‑203‑3p targets the 3'‑untranslated region of Smad1, which is an important mediator of the bone morphogenetic protein (BMP)/Smad pathway. Overexpression of Smad1 attenuated the miR‑203‑3p‑mediated suppres-sion of osteogenic differentiation. It was therefore indicated that the BMP/Smad pathway is attenuated and the transforming growth factor‑β/activin pathway is promoted by Smad1 reduction. Taken together, it was indicated that miR‑203‑3p inhibits osteogenesis in jaw bones of diabetic rats by targeting Smad1 to inhibit the BMP/Smad pathway.
- Subjects :
- Animals
Base Sequence
Down-Regulation drug effects
Down-Regulation genetics
Gene Expression Profiling
Glucose toxicity
Male
Mandible metabolism
MicroRNAs genetics
Models, Biological
Osteogenesis drug effects
Rats, Sprague-Dawley
Smad1 Protein metabolism
Diabetes Mellitus, Experimental genetics
Jaw metabolism
MicroRNAs metabolism
Osteogenesis genetics
Smad1 Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1791-244X
- Volume :
- 41
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- International journal of molecular medicine
- Publication Type :
- Academic Journal
- Accession number :
- 29328402
- Full Text :
- https://doi.org/10.3892/ijmm.2018.3373