癌变·畸变·突变 ›› 2009, Vol. 21 ›› Issue (3): 234-237.doi: 10.3969/j.issn.1004-616x.2009.03.019

• 技术与方法 • 上一篇    下一篇

大鼠卵巢颗粒细胞的原代培养与鉴定

许 川1, 舒为群1, 张 亮1, 曹 佳2, 周 新3   

  1. 1.第三军医大学军事预防医学院环境卫生学教研室, 重庆 400038; 2. 第三军医大学军事预防医学院军事毒理学教研室, 重庆 400038;3. 第三军医大学西南医院烧伤科, 重庆 400038
  • 收稿日期:2008-10-27 修回日期:2008-12-24 出版日期:2009-05-30 发布日期:2009-05-30

Culture and Identification of Granulosa Cells from Rat Ovary

XU Chuan1, SHU Wei-qun1, ZHANG Liang1, CAO Jia2, ZHOU Xin3   

  1. 1. Department of Environmental Hygiene, School of Military Preventive Medicine, Third Military Medical University, Chongqing 400038; 2. Department of Toxicology, School of Military Preventive Medicine, Third Military Medical University, Chongqing 400038; 3.Institute of Burn Research, Southwestern Hospital,Third Military Medical University, Chongqing 400038,China
  • Received:2008-10-27 Revised:2008-12-24 Online:2009-05-30 Published:2009-05-30

摘要: 背景与目的: 探讨大鼠卵巢高纯度颗粒细胞培养及鉴定的方法,建立一种简便、稳定的细胞模型。 材料与方法: 选用SD雌性大鼠(21~25 d),皮下注射孕马血清促性腺激素(PMSG),48 h后用颈椎脱臼法处死,剖取双侧卵巢,采用机械分离方法释放卵巢颗粒细胞,0.25%胰蛋白酶消化结合低速离心分离细胞,用含15%胎牛血清的DMEM/F12培养基,置于37 ℃,5% CO2培养箱培养。以HE染色和卵泡刺激素受体(FSHR)免疫组化染色对所培养的卵巢颗粒细胞进行鉴定,用MTT法绘制细胞生长曲线,并检测细胞培养液雌二醇(E2)和孕酮(P)的分泌量。 结果: 分离培养的卵巢颗粒细胞存活率>90%,细胞纯度达到95%以上;体外培养的颗粒细胞对数生长期为48~96 h;颗粒细胞具有正常的分泌雌激素功能,在培养24 h细胞培养液中E2和P的分泌量分别为(10.36±15.89) pg/ml和(77.91± 17.24) pg/ml。 结论: 采用机械分离法结合胰蛋白酶消化及低速离心法分离培养的卵巢颗粒细胞纯度高、活性好,用FSHR表达染色鉴定颗粒细胞是一种简便快速的方法。

关键词: 大鼠, 卵巢, 颗粒细胞, 培养, 鉴定

Abstract: BACKGROUND AND AIM: To obtain and identify cultured granulosa cells from the ovary of rats so as to establish a convenient and stable experimental model. MATERIALS AND METHODS: Female SD rats were subcutaneously treated with pregnant mare serum gonadotropin (PMSG). Forty-eight hours after dosing with PMSG, the animals were decapitated and the ovaries were aseptically removed. Granulosa cells were then released by mechanical method, trypsin digestion and low-speed centrifugation separation were used for granulosa cells isolation. Granulosa cells were diluted and incubated in fresh DMEM-Ham's F-12 medium (1∶1) containing 15% of fetal bovine serum at 37 ℃ in water-saturated environment of 5% CO2. Hematoxylin & Eosin (HE) and immunohistochemical staining of FSHR were used for ovarian granulosa cell identification. Additionally, the growth curves of granulosa cells and hormone levels at different incubation times were evaluated as well. RESULTS: Over 95% of the cultured cells were ovarian granulosa cells.The exponential phase of growth was between 48 and 96 hours of incubation. CONCLUSION: More than 95% of highly purified granulosa cells could be obtained by mechanical method combined with trypsin digestion and low-speed centrifugation. Moreover, identifications of granulosa cells by HE and FSHR staining were quick and convenient approaches.

Key words: rat, ovary, granulosa cell, culture, identification