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脂多糖干预卵巢切除小鼠骨髓间充质干细胞的成骨分化能力
引用本文:刘大勇,王梅蕊,兰玲玲,赵梦明,贾 智. 脂多糖干预卵巢切除小鼠骨髓间充质干细胞的成骨分化能力[J]. 中国组织工程研究, 2014, 18(14): 2219-2225. DOI: 10.3969/j.issn.2095-4344.2014.14.014
作者姓名:刘大勇  王梅蕊  兰玲玲  赵梦明  贾 智
作者单位:天津医科大学口腔医院牙体牙髓科,天津市 300070
基金项目:国家自然科学基金面上项目(81371109):IGFBP5在牙周膜干细胞介导组织再生中的作用及分子机制研究
摘    要:
背景:骨平衡被打破造成的绝经后骨质疏松往往是由炎症因子的升高造成的,在牙周组织中,炎症致病菌可产生破坏宿主组织的毒性因子,如脂多糖、菌毛、凝集素等。目的:通过建立卵巢切除小鼠骨质疏松的模型,观察脂多糖刺激下骨髓间充质干细胞成骨分化能力的改变,初步探讨雌激素缺乏患者易患牙周炎的细胞分子生物学机制,为绝经后妇女牙周炎的防治提供实验基础。方法:30只雌性昆明小鼠随机均分为卵巢切除组和对照组。取两组小鼠的骨髓间充质干细胞进行成骨诱导,同时加入不同质量浓度脂多糖(0,10,100 μg/L)刺激,检测碱性磷酸酶染色、茜素红染色以及碱性磷酸酶活性;RT-PCR之后检测成骨相关分子Runx2、Ocn、Alp的表达。结果与结论:成骨诱导7 d后可表达碱性磷酸酶,21 d后茜素红染色阳性,可形成矿化结节。检测发现成骨相关分子Ocn、Runx2、Alp的mRNA在成骨诱导后均有表达;3种目的基因在100 μg/L脂多糖作用下表达显著下降(P < 0.05),卵巢切除小鼠骨髓间充质干细胞在脂多糖作用下3种基因表达较对照组下降显著(P < 0.05)。卵巢切除小鼠骨髓间充质干细胞的成骨分化能力下降;脂多糖使骨髓间充质干细胞的成骨分化能力下降,卵巢切除组小鼠骨髓间充质干细胞成骨分化能力在脂多糖作用下明显减弱,这可能是雌激素缺乏导致牙周炎易感性增加的细胞分子学机制之一。中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程全文链接:

关 键 词:干细胞  骨髓干细胞  骨质疏松症  牙周炎  骨髓间充质干细胞  脂多糖  成骨分化  
收稿时间:2014-02-25

Lipopolysaccharide effects on osteogenic differentiation of bone marrow mesenchymal stem cells derived from ovariectomized mice
Liu Da-yong,Wang Mei-rui,Lan Ling-ling,Zhao Meng-ming,Jia Zhi. Lipopolysaccharide effects on osteogenic differentiation of bone marrow mesenchymal stem cells derived from ovariectomized mice[J]. Chinese Journal of Tissue Engineering Research, 2014, 18(14): 2219-2225. DOI: 10.3969/j.issn.2095-4344.2014.14.014
Authors:Liu Da-yong  Wang Mei-rui  Lan Ling-ling  Zhao Meng-ming  Jia Zhi
Affiliation:Department of Endodontics, Hospital of Stomatology, Tianjin Medical University, Tianjin 300070, China
Abstract:
BACKGROUND:Postmenopausal osteoporosis often results from upregulation of inflammatory factors. Pathogenic bacteria in periodontal tissues can generate some virulence factors destroying host tissues, such as lipopolysaccharide, pilus, and lectin. OBJECTIVE: To investigate osteogenic differentiation property of bone marrow mesenchymal stem cells under lipopolysaccharide stimulation in ovariectomized mice, and to preliminarily explore the cellular and molecular biological mechanisms underlying estrogen deficiency patients susceptible to periodontitis, which attempting to provide laboratory evidences for periodontitis prevention of postmenopausal women.  METHODS: Thirty female two-month-aged Kunming mice were randomly divided into ovariectomized group and sham group. Two groups of bone marrow mesenchymal stem cells were subject to osteogenic induction and cultured in media containing different concentrations of lipopolysaccharide (0, 10, 100 μg/L). After osteogenic inductions, alkaline phosphatase staining and alizarin red staining were performed, and expression of Runx2, Ocn, Alp were detected using RT-RCR. RESULTS AND CONCLUSION: After 7 days of osteogenic differentiation, cells expressed alkaline phosphatase; after 21 days, alizarin red staining was positive and mineralized nodules were visible. mRNA expressions of Ocn, Runx2, and Alp in 100 μg/L lipopolysaccharide group were significantly decreased (P < 0.05). Compared with the control group, the expressions of three target genes were significantly declined after intervention with lipopolysaccharide (P < 0.05). These findings indicate that lipopolysaccharide reduces the osteogenic ability of bone marrow mesenchymal stem cells, especially in ovariectomized mice, which may be one of cellular and molecular mechanisms by which estrogen deficiency leads to increased susceptibility of periodontitis.
Keywords:tem cells  mesenchymal stem cells  bone marrow  periodontitis  osteoporosis  lipopolysaccharides  
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