The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, China.
The Second Clinical Medical College, Fujian Medical University, Fuzhou, 350000, China.
BMC Musculoskelet Disord. 2022 Apr 9;23(1):340. doi: 10.1186/s12891-022-05266-0.
Macrophages are one of the important cells in immune system. In this article, we aim to explore the regulatory role of miR-455-3p on proliferation and osteoblast differentiation of RAW264.7 cells.
Expression levels of genes and proteins in cells were tested via qRT-PCR and western blot. The targeted correlation between miR-455-3p and PTEN was identified by luciferase analysis. MTT assay and flow cytometry were applied to detect the proliferation and apoptosis of cells. Osteoclastogenesis was completed by stimulating RAW 264.7 cells with RANKL. Tartrate-resistant acid phosphatase (TRAP) activity in different groups of cells were assessed.
Firstly, we determined that up-regulation of miR-455-3p promoted the proliferation and inhibited apoptosis of RAW 264.7 cells. MiR-455-3p deficiency played opposite effect in RAW 264.7 cells. Additionally, osteoclastogenesis-related factors (TRAP, CTSK and NFATc1) expression levels were remarkably up-regulated in miR-455-3p-mimic group of RAW264.7 cells treated with RANKL, but decreased in inhibitor group. Luciferase assay proved that miR-455-3p targeted PTEN. We took a further step and found overexpression of PTEN significantly inhibited the increased proliferation and osteoblast differentiation of RAW264.7 cells induced by miR-455-3p.
Our findings supported basic to explore the molecular mechanism of proliferation and osteoblast differentiation of RAW264.7 cells.
巨噬细胞是免疫系统中的重要细胞之一。在本文中,我们旨在探讨 miR-455-3p 对 RAW264.7 细胞增殖和成骨分化的调节作用。
通过 qRT-PCR 和 Western blot 检测细胞中基因和蛋白的表达水平。通过荧光素酶分析鉴定 miR-455-3p 与 PTEN 之间的靶向相关性。MTT 检测和流式细胞术用于检测细胞的增殖和凋亡。通过用 RANKL 刺激 RAW 264.7 细胞来完成破骨细胞分化。评估不同组细胞中抗酒石酸酸性磷酸酶(TRAP)活性。
首先,我们确定上调 miR-455-3p 促进了 RAW 264.7 细胞的增殖并抑制了其凋亡。miR-455-3p 缺失在 RAW 264.7 细胞中则起到相反的作用。此外,在 RANKL 处理的 RAW264.7 细胞中,破骨细胞分化相关因子(TRAP、CTSK 和 NFATc1)的表达水平显著上调,但在抑制剂组中则降低。荧光素酶实验证实 miR-455-3p 靶向 PTEN。我们进一步发现,过表达 PTEN 显著抑制了 miR-455-3p 诱导的 RAW264.7 细胞增殖和成骨分化的增加。
我们的研究结果支持进一步探索 RAW264.7 细胞增殖和成骨分化的分子机制。