CHANGES OF WNT/B-CATENIN SIGNALING AND DIFFERENTIATION POTENTIAL OF BONE MARROW MESENCHYMAL STEM CELLS IN PROCESS OF BONE LOSS IN OVARIECTOMIZED RATS

被引:4
|
作者
Ren, W. [1 ]
Gan, D. [2 ]
Tan, G. [2 ]
Xue, H. [2 ]
Li, N. [2 ]
Xu, Z. [2 ]
机构
[1] Weifang Hosp TCM, Weifang, Peoples R China
[2] Shandong Univ TCM, Affiliated Hosp, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
Postmenopausal osteoporosis; BMSCs; Wnt/beta-catenin signalling; Osteoblastic differentiation; Adipogenic differentiation; OSTEOGENIC DIFFERENTIATION; ADIPOSE-TISSUE; OSTEOBLASTOGENESIS; ANGIOGENESIS;
D O I
10.4183/aeb.2020.156
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. In vitro studies of the changes about osteoblastogenesis and adipogenesis potential of BMSCs were not clear. As it is the critical pathway for osteogenic differentiation and bone formation, whether or not Wnt/beta-catenin signalling is involved in the changes of osteogenic and adipogenic potential of BMSCs and participates in bone content decrease of ovariectomized (OVX)osteoporosis rats has been rarely reported. Material/Methods. BMSCs from femurs of ovariectomzed rats were isolated and cultured in vitro. The proliferation potential of BMSCs was analysed by CCK-8 assays . Osteoblastic and adipogenic differentiation potential of the BMSCs was assessed by ALP activity assay, Alizarin red S staining, Oil red O staining and RT-PCR analysis. Results. The results demonstrated that BMSCs from bilateral ovariectomization rats were endowed with lower proliferation and osteoblastic differentiation potential but higher adipogenic potential than the control group in vitro. In addition, beta-catenin was found to have been decreased in OVX BMSCs, indicating that Wnt/beta-catenin signalling pathways were suppressed in OVX BMSCs . Conclusions. Results suggested that changes in the Wnt canonical signalling pathway may be related to imbalances of osteogenic and adipogenic potential of BMSCs, and this may be an important factor related to bone content decrease in ovariectomized osteoporosis rats.
引用
收藏
页码:156 / 164
页数:9
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