MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19
Abstract Background To investigated the role of miR-19b-3p in regulating bone marrow mesenchymal stem cell (BMSC) proliferation and osteoblast differentiation. Methods The expression of miR-19b-3p and lncRNA H19 were measured in postmenopausal osteoporosis patients and BMP-22 induced BMSCs using qRT...
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BMC
2020-01-01
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Online Access: | https://doi.org/10.1186/s12881-020-0948-y |
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author | Gan Xiaoling Liu Shuaibin Liang Kailu |
author_facet | Gan Xiaoling Liu Shuaibin Liang Kailu |
author_sort | Gan Xiaoling |
collection | DOAJ |
description | Abstract Background To investigated the role of miR-19b-3p in regulating bone marrow mesenchymal stem cell (BMSC) proliferation and osteoblast differentiation. Methods The expression of miR-19b-3p and lncRNA H19 were measured in postmenopausal osteoporosis patients and BMP-22 induced BMSCs using qRT-PCR. MiR-19b-3p mimic or inhibitor was transfected into BMP-2 induced BMSCs. Cell proliferation was measured by BrdU method. Protein expression of RUNX2 and COL1A1 were measured by western blot. PcDNA3.1-lncRNA H19 with or without miR-19b-3p mimic was transfected into BMP-2 induced BMSCs. Results The expression of miR-19b-3p was significantly up-regulated in postmenopausal osteoporosis patients and BMP-2 induced BMSCs. MiR-19b-3p overexpression dramatically elevated, while miR-19b-3p inhibition decreased cell proliferation of BMSCs. Additionally, protein expression levels of RUNX2 and COL1A1, as well as ALP activity were significantly promoted by miR-19b-3p mimic transfection and inhibited by miR-19b-3p inhibitor transfection. LncRNA H19 was obviously down-regulated in postmenopausal osteoporosis patients. H19 overexpression significantly decreased cell proliferation and differentiation by down-regulating miR-19b-3p. Moreover, the expression of miR-19b-3p was inhibited, while H19 elvated in 17β-estradiol (E2) treated BMSCs in a dose-dependent manner. Conclusion These data were the first to reveal the critical role of H19/miR-19b-3p in postmenopausal osteoporosis, and provided a new therapeutic target for OP. |
first_indexed | 2024-12-16T12:19:04Z |
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id | doaj.art-3000987850d64a9db17bf09ad6c6d9d3 |
institution | Directory Open Access Journal |
issn | 1471-2350 |
language | English |
last_indexed | 2024-12-16T12:19:04Z |
publishDate | 2020-01-01 |
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series | BMC Medical Genetics |
spelling | doaj.art-3000987850d64a9db17bf09ad6c6d9d32022-12-21T22:32:01ZengBMCBMC Medical Genetics1471-23502020-01-012111810.1186/s12881-020-0948-yMicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19Gan Xiaoling0Liu Shuaibin1Liang Kailu2Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Chongqing Medical UniversityDepartment of Obstetrics and Gynecology, The Second Affiliated Hospital of Chongqing Medical UniversityDepartment of Orthopedics, The Second Affiliated Hospital of Chongqing Medical UniversityAbstract Background To investigated the role of miR-19b-3p in regulating bone marrow mesenchymal stem cell (BMSC) proliferation and osteoblast differentiation. Methods The expression of miR-19b-3p and lncRNA H19 were measured in postmenopausal osteoporosis patients and BMP-22 induced BMSCs using qRT-PCR. MiR-19b-3p mimic or inhibitor was transfected into BMP-2 induced BMSCs. Cell proliferation was measured by BrdU method. Protein expression of RUNX2 and COL1A1 were measured by western blot. PcDNA3.1-lncRNA H19 with or without miR-19b-3p mimic was transfected into BMP-2 induced BMSCs. Results The expression of miR-19b-3p was significantly up-regulated in postmenopausal osteoporosis patients and BMP-2 induced BMSCs. MiR-19b-3p overexpression dramatically elevated, while miR-19b-3p inhibition decreased cell proliferation of BMSCs. Additionally, protein expression levels of RUNX2 and COL1A1, as well as ALP activity were significantly promoted by miR-19b-3p mimic transfection and inhibited by miR-19b-3p inhibitor transfection. LncRNA H19 was obviously down-regulated in postmenopausal osteoporosis patients. H19 overexpression significantly decreased cell proliferation and differentiation by down-regulating miR-19b-3p. Moreover, the expression of miR-19b-3p was inhibited, while H19 elvated in 17β-estradiol (E2) treated BMSCs in a dose-dependent manner. Conclusion These data were the first to reveal the critical role of H19/miR-19b-3p in postmenopausal osteoporosis, and provided a new therapeutic target for OP.https://doi.org/10.1186/s12881-020-0948-ymiR-19b-3plncRNA H19OsteoporosisPostmenopausalBMSC |
spellingShingle | Gan Xiaoling Liu Shuaibin Liang Kailu MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 BMC Medical Genetics miR-19b-3p lncRNA H19 Osteoporosis Postmenopausal BMSC |
title | MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 |
title_full | MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 |
title_fullStr | MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 |
title_full_unstemmed | MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 |
title_short | MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 |
title_sort | microrna 19b 3p promotes cell proliferation and osteogenic differentiation of bmscs by interacting with lncrna h19 |
topic | miR-19b-3p lncRNA H19 Osteoporosis Postmenopausal BMSC |
url | https://doi.org/10.1186/s12881-020-0948-y |
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