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作 者:廖立凡 李昱 杨琳 杨欣 LIAO Lifan;LI Yu;YANG Lin;YANG Xin(Key Laboratory of Shaanxi Province for CraniofacialPrecision Medicine Research,Department of Implant Dentistry,College of Stomatology,Xi'an Jiaotong University,China,710004;Urumqi,Department of Oral and Maxillofacial Surgery,General Hospital of Xinjiang Military Region)
机构地区:[1]西安交通大学口腔医院陕西省颅颌面精准医学研究重点实验室,西安交通大学口腔医院种植科,710004 [2]新疆军区总医院口腔颌面外科
出 处:《实用口腔医学杂志》2022年第3期317-321,共5页Journal of Practical Stomatology
基 金:西安市创新能力强基计划-医学研究项目(编号:21YXYJ0124);新疆维吾尔自治区自然科学基金面上项目(编号:2021D01C473)。
摘 要:目的:研究Runt相关转录因子-2(Runx2)缺失对小鼠颞下颌关节(TMJ)髁突软骨细胞的肥大分化及其生物力学性能的影响。方法:创建Runx2^(Agc1CreER)条件性敲除小鼠及其同窝对照小鼠(Cre^(-))模型。采用组织学切片观察、免疫组化染色以及纳米弹性模量检测方法,比较两组小鼠髁突软骨细胞分化及生物力学特性的差异。结果:Runx2敲除导致软骨肥大层丧失以及软骨基质生成减少,髁突软骨中ColX、IHH、PCNA表达显著降低。Runx2^(Agc1CreER)组和Cre^(-)组小鼠髁突软骨纳米弹性模量(MPa)分别为0.0898和0.7620(P<0.05)。结论:Runx2缺失干扰出生后小鼠TMJ髁突软骨细胞肥大分化过程,影响髁突软骨的力学性能。Objective:To investigate of Runx2 gene knockout on the hypertrophic differentiation of chondrocytes and biomechanical properties of the condyle of mice.Methods:Runx2 knockout mice(Runx2^(Agc1CreER))and its littermate control mice(Cre^(-))were used for the study.Histological observation,immunohistochemical staining and nanoindentation test were performed to compare the similarities and differences of the hypertrophic diffentiation and biomechanics between the 2 groups of mice.Results:HE staining observation and immunohistochemical results showed that the lack of Runx2 led to the loss of hypertrophic cartilage layer and reduction of cartilage matrix production in Runx2^(Agc1CreER) mice.The expressions of ColX,IHH and PCNA in the condylar cartilage of Runx2^(Agc1CreER) mice were significantly reduced.The nano-elastic modulus(MPa)of the condylar cartilage of Cre^(-) and Runx2^(Agc1CreER) mice was 0.0898 and 0.7620 respectively(P<0.05).Conclusion:Runx2 is necessary for the hypertrophic differentiation of TMJ condylar chondrocytes in mice after birth.Knockout Runx2 may increase the elastic modulus of condyle cartilage.
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