Suppr超能文献

[RAW264.7破骨细胞的骨吸收上清液对小鼠MC3T3-E1细胞成骨活性的影响]

[Effect of the bone resorption supernatant from RAW264.7 osteoclast on the osteogenic activity of mouse MC3T3-E1 cell].

作者信息

Chen Li-li, Wang Kai, Zhang Jie, Wu Yan-min

机构信息

Department of Oral Medicine, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310009, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2012 Jan;47(1):32-7. doi: 10.3760/cma.j.issn.1002-0098.2012.01.012.

Abstract

OBJECTIVE

To investigate the effect of osteoclast bone resorption supernatants on the osteogenic activity of mouse MC3T3-E1 cell line.

METHODS

Mouse RAW264.7 cell line was induced to osteoclast which was identified with tartrate resistant acid phosphatase (TRAP) staining and osteoclast specific gene detection. The differentiated RAW264.7 osteoclast was co-cultured with bovine milling bone specimen followed by toluidine blue staining. Then mouse MC3T3-E1 cell was cultured with supernatant from the osteoclast bone absorbent model. Methyl thiazolyl tetrazolium (MTT) method, alizarin red S staining, enzyme-linked immunosorbent assay detection of osteocalcin, and reverse transcriptase polymerase chain reaction detection were adopted to investigate the proliferation, calcification and osteogenic activity of MC3T3-E1 cells.

RESULTS

TRAP staining, osteoclast specific gene detection and toluidine blue staining all indicated that RAW264.7 cell could be differentiated into functioning osteoclast. The supernatant from the osteoclast bone absorbent model could inhibit the proliferation of MC3T3-E1 cells, with the A value between 0.062 ± 0.004 and 0.405 ± 0.033 (P < 0.05). It could also increase the formation of calcification nods, promote the osteocalcin level which peaked with the tenth day's supernatant at a level of (2.965 ± 0.047) µg/L, as well as enhance the transcription of the alkaline phosphatase and Runt related transcription factor 2 gene.

CONCLUSIONS

RAW264.7 osteoclast bone absorbent supernatant might influence the osteogenic activity of osteoblast-like cell by inhibiting proliferation, promoting differentiation and calcification.

摘要

目的

探讨破骨细胞骨吸收上清液对小鼠MC3T3-E1细胞系成骨活性的影响。

方法

诱导小鼠RAW264.7细胞系成为破骨细胞,通过抗酒石酸酸性磷酸酶(TRAP)染色和破骨细胞特异性基因检测进行鉴定。将分化后的RAW264.7破骨细胞与牛磨碎骨标本共培养,随后进行甲苯胺蓝染色。然后用破骨细胞骨吸收模型的上清液培养小鼠MC3T3-E1细胞。采用甲基噻唑基四氮唑(MTT)法、茜素红S染色、酶联免疫吸附测定法检测骨钙素以及逆转录聚合酶链反应检测,以研究MC3T3-E1细胞的增殖、钙化和成骨活性。

结果

TRAP染色、破骨细胞特异性基因检测和甲苯胺蓝染色均表明RAW264.7细胞可分化为有功能的破骨细胞。破骨细胞骨吸收模型的上清液可抑制MC3T3-E1细胞的增殖,A值在0.062±0.004至0.405±0.033之间(P<0.05)。它还可增加钙化结节的形成,促进骨钙素水平升高,第10天上清液时达到峰值,水平为(2.965±0.047)μg/L,同时增强碱性磷酸酶和Runt相关转录因子2基因的转录。

结论

RAW264.7破骨细胞骨吸收上清液可能通过抑制增殖、促进分化和钙化来影响成骨样细胞的成骨活性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验