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四种小鼠破骨细胞体外诱导培养方法的比较
引用本文:刘华清,李冰燕,张增利.四种小鼠破骨细胞体外诱导培养方法的比较[J].劳动医学,2011(9):556-560.
作者姓名:刘华清  李冰燕  张增利
作者单位:苏州大学医学部放射医学与公共卫生学院,江苏省放射医学与防护重点实验室,江苏苏州215123
基金项目:国家自然科学基金资助项目(编号:30972467);江苏省自然科学基金资助项目(编号:BK2009120)
摘    要:目的]比较不同的破骨细胞体外诱导培养方法,为研究外源性因素对骨代谢影响提供方法学基础。方法]采用骨髓基质细胞和骨髓单核细胞三维共育、骨髓基质细胞培养液转移刺激骨髓单核细胞、重组核因子-κB受体激活物配基(RANKL)诱导骨髓单核细胞和RANKL诱导单核巨噬细胞株RAW264.7四种方法体外诱导破骨细胞。活细胞示踪剂CM-DiI标记RAW264.7后,用激光共聚焦显微镜扫描观察破骨细胞形成过程;抗酒石酸酸性磷酸酶(TRAP)染色法染色破骨细胞。结果]四种方法均成功地诱导培养出由多个细胞互相融合的TRAP阳性多核破骨细胞。加入RANKL的方法诱导出的破骨细胞较大,数量也较多,方法简单。正常骨髓基质细胞诱导形成的破骨细胞形态较小,数量也相对较少,过程复杂,但可以用来研究干预因素作用于骨髓基质细胞后对破骨细胞分化的间接影响。在对照组及诱导培养体系中均可观察到一类不互相融合的TRAP阳性细胞,含1~3个核,TRAP染色多集中在胞核周围,此类细胞可能是尚未分化的破骨细胞前体。而互相融合的破骨细胞TRAP染色见于整个胞浆。结论]各种破骨细胞体外诱导培养方法各有优势,应根据不同的实验目的选用不同的破骨细胞诱导培养方法。

关 键 词:破骨细胞  抗酒石酸盐磷酸酶(TRAP)染色  核因子-κB受体配基(RANKL)  骨髓基质细胞  小鼠单核巨噬细胞白血病细胞(RAW264.7)

Comparison of Four in vitro Osteoclast Culture Systems
LIU Hua-qing,LI Bing-yan,ZHANG Zeng-li.Comparison of Four in vitro Osteoclast Culture Systems[J].Journal of Labour Medicine,2011(9):556-560.
Authors:LIU Hua-qing  LI Bing-yan  ZHANG Zeng-li
Institution:(Department of Toxicology, School of Radiation Medicine and Public Health, Soochow University/diangsu Provincial Key Laboratory of Radiation Medicine and Protection, Suzhou, Jiangsu, 215123, China).
Abstract:For studying effects of exogenous factors on bone metabolism, different in vitro osteoclast (OC) culture systems were compared in this study. Methods ] Bone marrow mononuclear cells co-cultured with bone marrow stromal cells (BMSC) in 3-dimensioal culture system, bone marrow mononuelear cells cultured with bone marrow stromal cells conditional medium, bone marrow mononuclear cells and RAW264.7 cell line cultured in the presence of mouse recombinant receptor activator of nuclear factorkappaB ligand (RANKL) for OC differentiation. RAW264.7 cells were labeled with cross-linkable membrane dye CM-DiI to examine the fusing process of OC differentiation by Laser Scanning Confocal Microscope. OC was stained by Tartrate Resistant Acid Phosphatase (TRAP). Results ] All of the procedures successfully developed OC which was indicated by TRAP positive and muhinuelear cells fusing from OC precursors. The OCs induced by exogenous RANKL were easy acquired, whose number and size were more and bigger than those induced by the normal BMSCs. The method of OC differentiation induced by normal BMSCs was complicated, but Was useful for studying the indirect effect of intervention factor on OC differentiation post treated BMSC. Some TRAP positive cells characterized by cell membrane not fusing and TRAP staining only focusing around nucleus were observed in all groups, and contained 1-3 nucleuses. This kind of TRAP positive cells might be OC precursors. Conclusion ] Each OC differentiation method shows various advantages and which specific procedure is selected should accord to study objectives.
Keywords:osteoclast  TRAP staining  RANKL  bone marrow stromal cells  RAW264  7
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