膜联蛋白A1在兔骨髓间充质干细胞体外诱导成骨和成脂早期的表达  被引量:1

Expression of annexin A1 in rabbit bone marrow mesenchymal stem cells during their early differentiation into osteoblasts and adipocytes in vitro

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作  者:潘新元[1] 梁博伟[2] 赵劲民[2] 殷国前[1] 

机构地区:[1]广西医科大学第一附属医院整形美容外科,广西壮族自治区南宁市530021 [2]广西医科大学第一附属医院创伤手外科,广西壮族自治区南宁市530021

出  处:《中国组织工程研究》2012年第23期4181-4186,共6页Chinese Journal of Tissue Engineering Research

基  金:国家自然科学基金资助项目(30860285);课题名称:早期激素性股骨头缺血性坏死的蛋白质组学动态分析~~

摘  要:背景:骨髓间充质干细胞分化过程中膜联蛋白A1表达变化的研究报道各有不同看法。目的:分析兔骨髓间充质干细胞在体外诱导成骨和成脂过程中膜联蛋白A1基因的表达变化。方法:应用全骨髓贴壁法分离培养骨髓间充质干细胞,分别加入含成骨诱导剂、成脂诱导剂及不添加任何诱导剂的培养基进行培养。结果与结论:膜联蛋白A1基因在成骨诱导过程中与未诱导细胞相比有明显下调趋势,差异有显著性意义(P<0.01),而在成脂诱导剂中则为上升(P<0.01)。成骨诱导剂对细胞生长存在抑制作用并增加细胞凋亡(P<0.01),而成脂诱导剂对细胞生长与凋亡作用较小(P>0.05)。因此排除了诱导剂对细胞的作用之后,推测膜联蛋白A1基因可能与骨髓间充质干细胞体外向脂肪细胞分化存在一定关系,但尚不能肯定其在成骨分化中的作用。BACKGROUND: Studies have reported different views on the expression of annexin A1 (ANX A1 ) in bone marrow mesenchymal stem cells (BMSCs) during their differentiation. OBJECTIVE: To investigate the expression of ANX A1 in rabbit BMSCs during their differentiation into osteoblasts and adipocytes in vitro. METHODS: BMSCs were isolated by whole bone marrow adherence method, and then the cells were cultured in media with osteogenic inducer, adipogenic inducer and non-inducer respectively. RESULTS AND CONCLUSION: The expression of ANX A1 mRNA was obviously decreased during the cell differentiation into osteoblasts compared with those without differentiation (P 〈 0.01 ). In contrast, the expression of ANX A1 mRNA was obviously increased in BMSCs cultured in medium with adipogenic inducer (P 〈 0.01 ). Osteogenic inducer could inhibit the growth of BMSCs to achicve an increase in apoptosis (P 〈 0.01 ), while the adipogenic inducer had little effects on cell growth and apoptosis (P 〉 0.05). ANX A1 may play an important role in regulation of BMSCs differentiation into adipocytes in vitro without the role of inducer. However, the association with osteogenic differentiation is uncertain.

关 键 词:膜联蛋白A1 骨髓间充质干细胞 体外诱导成骨、成脂 荧光定量RT-PCR 干细胞 

分 类 号:R394.2[医药卫生—医学遗传学]

 

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