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Non-coding RNAs regulate the BMP/Smad pathway during osteogenic differentiation of stem cells.

Authors :
Zhang Q
Long Y
Jin L
Li C
Long J
Source :
Acta histochemica [Acta Histochem] 2023 Jan; Vol. 125 (1), pp. 151998. Date of Electronic Publication: 2023 Jan 09.
Publication Year :
2023

Abstract

MicroRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs) are involved in the regulation of bone metabolism. The BMP/Smad pathway is a key signaling pathway for classical regulation of osteogenic differentiation. Non-coding RNAs (ncRNAs) and the BMP/Smad pathway both have important roles for osteogenic differentiation of stem cells, bone regeneration, and development of bone diseases. There is increasing evidence that ncRNAs interact with the BMP/Smad pathway to regulate not only osteogenic differentiation of stem cells but also progression of bone diseases, such as osteoporosis (OP), myeloma, and osteonecrosis of the femoral head (ONFH), by controlling the expression of bone disease-related genes. Therefore, ncRNAs that interact with BMP/Smad pathway molecules are potential targets for bone regeneration as well as bone disease diagnosis, prevention, and treatment. However, despite extensive studies on ncRNAs associated with the BMP/Smad pathway and osteogenic differentiation of stem cells, there is a lack of comparability. Moreover, some bone disease-associated ncRNAs with low abundance can be difficult to detect and there is a lack of mature delivery systems for their stable translocation to target sites, thus limiting their application. In this review, we summarize the research progress on interactions between ncRNAs and the BMP/Smad pathway during osteogenic differentiation of various stem cells and in the regulation of bone regeneration and bone diseases.<br />Competing Interests: Conflict of interest The authors declare that they have no conflicts of interest.<br /> (Copyright © 2023 Elsevier GmbH. All rights reserved.)

Details

Language :
English
ISSN :
1618-0372
Volume :
125
Issue :
1
Database :
MEDLINE
Journal :
Acta histochemica
Publication Type :
Academic Journal
Accession number :
36630753
Full Text :
https://doi.org/10.1016/j.acthis.2023.151998