[Expression profiles of CaMKIIγ during osteoclast differentiation]

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2018 Mar 28;43(3):240-245. doi: 10.11817/j.issn.1672-7347.2018.03.002.
[Article in Chinese]

Abstract

To study the expression profiles and the role of Ca2+/calmodulin-dependent protein kinase IIγ (CaMKIIγ) during osteoclast differentiation. Methods: Mouse RAW264.7 cells were induced for osteoclastogenesis with 50 ng/mL receptor activator of nuclear factor-κB ligand (RANKL) and the cells were harvested at 0, 1, 3 and 5 days after induction. Tartrate-resistant acid phosphotase staining was performed to verify osteoclasts formation. RT-PCR, Western blot and immunofluorescent cytochemistry were used to detect the CaMKIIγ gene expression during osteoclastogenesis. Results: The osteoclasts were formed at day 3 under RANKL induction and more osteoclasts were observed at day 5. At day 0, 1, 3 and 5, the relative level of CaMKIIγ mRNA were (1.067±0.179), (1.840±0.070), (9.493±0.453) and (30.767±0.573), respectively, and the relative protein level were (0.454±0.065), (0.613±0.021), (0.858±0.019) and (0.980±0.023), respectively. CaMKIIγ expression was increased in a time-dependent manner except relative protein level at day 1 (P<0.01), which showed no significant difference at day 0 (P>0.05). Immunofluorescence assay showed that CaMKIIγ protein was also increased with differentiation of osteoclasts. Conclusion: The CaMKIIγ expression was increased in a time-depended manner during osteoclast differentiation and it might play a vital role during osteoclastogenesis.

目的:研究钙离子/钙调蛋白依赖性激酶γ(CaMKIIγ)在破骨细胞分化中的表达规律,以揭示其作用。 方法:用50 ng/mL核因子-κB受体活化因子配体(RANKL)诱导RAW264.7细胞向破骨细胞分化,于诱导后第0,1,3,5天收获细胞,用抗酒石酸酸性磷酸酶(TRAP)染色评价破骨细胞生成情况,并用RT-PCR、Western印迹、免疫荧光细胞化学法检测CaMKIIγ mRNA和蛋白表达。结果:多核破骨细胞在诱导后第3天开始出现,第5天达到最多。分化第0,1,3,5天,CaMKIIγ mRNA相对表达水平分别为(1.067±0.179),(1.840±0.070),(9.493±0.453)和(30.767±0.573);蛋白相对表达水平分别为(0.454±0.065),(0.613±0.021),(0.858±0.019)和(0.980±0.023);除第1天的蛋白相对水平外,其他时间点CaMKIIγ mRNA和蛋白表达差异均有统计学意义,且呈时间依赖性增强(P<0.01)。免疫荧光细胞化学法检测也显示CaMKIIγ蛋白表达在破骨细胞分化过程中逐步增加。结论:CaMKIIγ表达随破骨细胞分化呈时间依赖性增加,提示其在破骨细胞分化中可能发挥关键调控作用。.

MeSH terms

  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism*
  • Cell Differentiation*
  • Cell Line
  • Gene Expression
  • Mice
  • Osteoclasts / cytology*
  • Osteoclasts / metabolism
  • Osteogenesis / drug effects
  • RANK Ligand / pharmacology
  • Time Factors

Substances

  • RANK Ligand
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2