The effect of mechanical stretch stress on the differentiation and apoptosis of human growth plate chondrocytes

被引:0
作者
Keming Sun
Fangna Liu
Junjian Wang
Zhanhao Guo
Zejuan Ji
Manye Yao
机构
[1] Zhengzhou Children’s Hospital,Department of Pediatric Orthopedics
来源
In Vitro Cellular & Developmental Biology - Animal | 2017年 / 53卷
关键词
Stretch stress; Growth plate; Chondrocytes; Differentiation; Apoptosis;
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中图分类号
学科分类号
摘要
The study is aimed to investigate the effect of stretch stress with different intensities on the differentiation and apoptosis of human plate chondrocytes. In the present study, the human epiphyseal plate chondrocytes were isolated and cultured in vitro. Toluidine blue staining and type II collagen immunohistochemical staining were used to identify the chondrocytes. Mechanical stretch stresses with different intensities were applied to intervene cells at 0-, 2000-, and 4000-μ strain for 6 h via a four-point bending system. The expression levels of COL2, COL10, Bax, Bcl-2, and PTHrp were detected by quantitative RT-PCR. Under the intervention of 2000-μ strain, the expression levels of COL2, COL10, and PTHrp increased significantly compared with the control group (P < 0.05), and the expression level of PCNA was also increased, but the difference was not statistically significant (P > 0.05). Under 4000-μ strain, however, the expression levels of PCNA, COL2, and PTHrp decreased significantly compared with the control group (P < 0.05), and the expression level of COL10 decreased slightly (P > 0.05). The ratio of Bcl-2/Bax gradually increased with the increase of stimulus intensity; both of the differences were detected to be statistically significant (P < 0.05). In conclusion, the apoptosis of growth plate chondrocytes is regulated by mechanical stretch stress. Appropriate stretch stress can effectively promote the cells’ proliferation and differentiation, while excessive stretch stress inhibits the cells’ proliferation and differentiation, even promotes their apoptosis. PTHrp may play an important role in this process.
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页码:141 / 148
页数:7
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共 106 条
[11]  
Yonenobu K(2002)Interaction of FGF, Ihh/Pthlh, and BMP signaling integrates chondrocyte proliferation and hypertrophic differentiation Dev Cell 3 439-449
[12]  
Nakase T(2003)Perspective. Osteoclastogenesis and growth plate chondrocyte differentiation: emergence of convergence Crit Rev Eukaryot Gene Expr 13 181-193
[13]  
Hosono N(2002)The effects of dynamic axial loading on the rat growth plate Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 17 284-292
[14]  
Okuda S(2012)Altered cellular kinetics in growth plate according to alterations in weight bearing Yonsei Med J 53 618-624
[15]  
Meng W(2001)Modulation of appositional and longitudinal bone growth in the rat ulna by applied static and dynamic force Bone 29 105-113
[16]  
Tamura Y(2011)Growth plate explants respond differently to in vitro static and dynamic loadings Journal of orthopaedic research : official publication of the Orthopaedic Research Society 29 473-480
[17]  
Yoshikawa H(2006)Endochondral growth in growth plates of three species at two anatomical locations modulated by mechanical compression and tension Journal of orthopaedic research : official publication of the Orthopaedic Research Society 24 1327-1334
[18]  
Cancel M(2007)Alterations in the growth plate associated with growth modulation by sustained compression or distraction Bone 41 197-205
[19]  
Grimard G(2003)Systemic and local regulation of the growth plate Endocr Rev 24 782-801
[20]  
Thuillard-Crisinel D(2007)The PTHrP-Ihh feedback loop in the embryonic growth plate allows PTHrP to control hypertrophy and Ihh to regulate proliferation Biomech Model Mechanobiol 6 55-62