Effect Of Mir-21 On Osteoclast Of Macrophage Raw264.7

This study aims to explore the effect of miR-21 on osteoclastic differentiation and proliferation of macrophage RAW264.7. RAW264.7 cells were transfected by lentiviral vector and divided into 4 groups: osteoclastic differentiation: OC marker genes (Ctsk, Mmp9, Acp5 and Nfatc1) were detected by RT-qPCR. Western blot was performed to detect the expression levels of Ctsk, Mmp and Pdcd4. proliferation: The optical density of the cells in each group were detected by CCK-8 at 1, 3, 5 and 7 days. The cell cycle of each group was detected by flow cytometry. After overexpression of miR-21, the number of osteoclasts, enzyme activity and concentration of TRAP, OC marker genes and Ctsk and Mmp9 were significantly increased, while the expression of Pdcd4 was down-regulated. However, the outcome is contrary after inhibition of miR-21 expression. There was no significant difference in RAW264.7 cell proliferation cycle and optical density at 1, 3, 5 and 7 days. MiR-21 can promote differentiation of RAW264.7 cells in vitro, and this process may be realized by regulating the expression of Pdcd4; and there was no significant effect of miR-21 on the proliferation of RAW264.7 cells.

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Publication Details

Journal
International Dental Journal
Published
2025-10-01
DOI
https://doi.org/10.1016/j.identj.2025.105366
Primary Topic
Bone Metabolism and Diseases
Type
article
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article

Effect Of Mir-21 On Osteoclast Of Macrophage Raw264.7

Long Qian, Meiling Xiang, Xiaoyan Guan, Mingli Xiang et al.
International Dental Journal
Bone Metabolism and Diseases
article

Effect Of Mir-21 On Osteoclast Of Macrophage Raw264.7

Long Qian, Meiling Xiang, Xiaoyan Guan, Mingli Xiang, Chengcheng Liao, Sicen Long
article en

Abstract

This study aims to explore the effect of miR-21 on osteoclastic differentiation and proliferation of macrophage RAW264.7. RAW264.7 cells were transfected by lentiviral vector and divided into 4 groups: osteoclastic differentiation: OC marker genes (Ctsk, Mmp9, Acp5 and Nfatc1) were detected by RT-qPCR. Western blot was performed to detect the expression levels of Ctsk, Mmp and Pdcd4. proliferation: The optical density of the cells in each group were detected by CCK-8 at 1, 3, 5 and 7 days. The cell cycle of each group was detected by flow cytometry. After overexpression of miR-21, the number of osteoclasts, enzyme activity and concentration of TRAP, OC marker genes and Ctsk and Mmp9 were significantly increased, while the expression of Pdcd4 was down-regulated. However, the outcome is contrary after inhibition of miR-21 expression. There was no significant difference in RAW264.7 cell proliferation cycle and optical density at 1, 3, 5 and 7 days. MiR-21 can promote differentiation of RAW264.7 cells in vitro, and this process may be realized by regulating the expression of Pdcd4; and there was no significant effect of miR-21 on the proliferation of RAW264.7 cells.

International Dental JournalVol. 75
Zunyi Medical University (CN)
Openalex Percentile: Top 71%
Bone Metabolism and Diseases
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Effect Of Mir-21 On Osteoclast Of Macrophage Raw264.7 — Long Qian, Meiling Xiang, et al. · International Dental Journal (2025) | TGRS Research Map | TGRS