MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head
Abstract Background It is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear. Methods The expression of miR-596 and Smad3 was detected by western blot and quantitative real-time PCR. The...
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Format: | Article |
Language: | English |
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BMC
2020-05-01
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Series: | Journal of Orthopaedic Surgery and Research |
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Online Access: | http://link.springer.com/article/10.1186/s13018-020-01688-5 |
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author | Ligong Fu Huawei Liu Weijun Lei |
author_facet | Ligong Fu Huawei Liu Weijun Lei |
author_sort | Ligong Fu |
collection | DOAJ |
description | Abstract Background It is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear. Methods The expression of miR-596 and Smad3 was detected by western blot and quantitative real-time PCR. The relationship between the two molecules was explored using Dual-Luciferase Reporter Assay. Glucocorticoid (GC)—dexamethasone, was used to induce bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation, and the effects of miR-596 on BMSC osteogenic differentiation and proliferation were determined. Results MiR-596 expression was upregulated, while Smad3 expression was inhibited in the bone marrow samples of patients with steroid-induced osteonecrosis of femoral head (SANFH). Overexpression of miR-596 inhibited the proliferation and osteogenic differentiation of BMSCs induced by GC. Meanwhile, the opposite results were observed in the miR-596 inhibitor group. In addition, Smad3 was a target gene of miR-596, and negatively regulated by miR-596. The promotion effect of the miR-596 inhibitor on BMSC proliferation and osteogenic differentiation was reversed by si-Smad3. Conclusion MiR-596 can suppress GC-BMSC osteoblastic differentiation and proliferation by regulating Smad3 expression. |
first_indexed | 2024-04-11T22:27:17Z |
format | Article |
id | doaj.art-44985fb224f544119e46e69a6441c43a |
institution | Directory Open Access Journal |
issn | 1749-799X |
language | English |
last_indexed | 2024-04-11T22:27:17Z |
publishDate | 2020-05-01 |
publisher | BMC |
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series | Journal of Orthopaedic Surgery and Research |
spelling | doaj.art-44985fb224f544119e46e69a6441c43a2022-12-22T03:59:37ZengBMCJournal of Orthopaedic Surgery and Research1749-799X2020-05-0115111010.1186/s13018-020-01688-5MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral headLigong Fu0Huawei Liu1Weijun Lei2Department of Orthopaedic Surgery, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua UniversityDepartment of Orthopaedic Surgery, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua UniversityDepartment of Orthopaedic Surgery, Hongze Huaian District People’s HospitalAbstract Background It is reported that miR-596 has a potential diagnostic value for non-traumatic osteonecrosis of the femoral head (NOFH), but its underlying mechanisms in NOFH is unclear. Methods The expression of miR-596 and Smad3 was detected by western blot and quantitative real-time PCR. The relationship between the two molecules was explored using Dual-Luciferase Reporter Assay. Glucocorticoid (GC)—dexamethasone, was used to induce bone marrow mesenchymal stem cell (BMSC) osteogenic differentiation, and the effects of miR-596 on BMSC osteogenic differentiation and proliferation were determined. Results MiR-596 expression was upregulated, while Smad3 expression was inhibited in the bone marrow samples of patients with steroid-induced osteonecrosis of femoral head (SANFH). Overexpression of miR-596 inhibited the proliferation and osteogenic differentiation of BMSCs induced by GC. Meanwhile, the opposite results were observed in the miR-596 inhibitor group. In addition, Smad3 was a target gene of miR-596, and negatively regulated by miR-596. The promotion effect of the miR-596 inhibitor on BMSC proliferation and osteogenic differentiation was reversed by si-Smad3. Conclusion MiR-596 can suppress GC-BMSC osteoblastic differentiation and proliferation by regulating Smad3 expression.http://link.springer.com/article/10.1186/s13018-020-01688-5Steroid-induced osteonecrosis of femoral headmiR-596Smad3Osteoblastic differentiationProliferation |
spellingShingle | Ligong Fu Huawei Liu Weijun Lei MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head Journal of Orthopaedic Surgery and Research Steroid-induced osteonecrosis of femoral head miR-596 Smad3 Osteoblastic differentiation Proliferation |
title | MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head |
title_full | MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head |
title_fullStr | MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head |
title_full_unstemmed | MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head |
title_short | MiR-596 inhibits osteoblastic differentiation and cell proliferation by targeting Smad3 in steroid-induced osteonecrosis of femoral head |
title_sort | mir 596 inhibits osteoblastic differentiation and cell proliferation by targeting smad3 in steroid induced osteonecrosis of femoral head |
topic | Steroid-induced osteonecrosis of femoral head miR-596 Smad3 Osteoblastic differentiation Proliferation |
url | http://link.springer.com/article/10.1186/s13018-020-01688-5 |
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