| Literature DB >> 34648701 |
Matthew L Potter1, Kathryn Smith2, Sagar Vyavahare2, Sandeep Kumar2, Sudharsan Periyasamy-Thandavan3, Mark Hamrick1,2,4, Carlos M Isales4,5, William D Hill6,7, Sadanand Fulzele1,2,4,5,1.
Abstract
Stromal cell-derived factor 1 (SDF-1) is known to influence bone marrow stromal cell (BMSC) migration, osteogenic differentiation, and fracture healing. We hypothesize that SDF-1 mediates some of its effects on BMSCs through epigenetic regulation, specifically via microRNAs (miRNAs). MiRNAs are small non-coding RNAs that target specific mRNA and prevent their translation. We performed global miRNA analysis and determined several miRNAs were differentially expressed in response to SDF-1 treatment. Gene Expression Omnibus (GEO) dataset analysis showed that these miRNAs play an important role in osteogenic differentiation and fracture healing. KEGG and GO analysis indicated that SDF-1 dependent miRNAs changes affect multiple cellular pathways, including fatty acid biosynthesis, thyroid hormone signaling, and mucin-type O-glycan biosynthesis pathways. Furthermore, bioinformatics analysis showed several miRNAs target genes related to stem cell migration and differentiation. This study's findings indicated that SDF-1 induces some of its effects on BMSCs function through miRNA regulation.Entities:
Keywords: SDF-1; bone marrow stromal cells; miRNA
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Year: 2021 PMID: 34648701 DOI: 10.1515/bmc-2021-0015
Source DB: PubMed Journal: Biomol Concepts ISSN: 1868-5021