胞红蛋白在缺氧神经元中的表达  被引量:1

Expression of cytoglobin in hypoxic neurons in vitro

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作  者:马海然[1] 史雪川[1] 

机构地区:[1]汕头大学医学院第二附属医院儿科,广东汕头515041

出  处:《中国儿童保健杂志》2014年第5期492-496,共5页Chinese Journal of Child Health Care

基  金:广东省科技计划项目(2008B080701036);广东省医学科研基金立项(B2009180)

摘  要:目的探讨细胞红蛋白(cytoglobin,CYGB)在体外培养神经元缺氧时的表达,为研究缺氧缺血性脑病(hypoxic ischemic encephalopathy,HIE)的生理病理机制及寻求该病新的治疗方法提供实验基础。方法运用无血清培养技术进行胎鼠皮质神经元原代培养6d;先用神经元特异性烯醇化酶免疫组织化学方法纯度鉴定,然后随机分配为4组,将其中3组(第1组作为对照)置于0.5%-0.9%的O2中,用CCK8试剂盒测试细胞生存率,同时用Real-timePCR和Westernblot观察CYGB在神经元正常及缺氧不同时间点(8h,16h,24h)核酸及蛋白的表达情况。结果神经元纯度鉴定纯度大于99%;缺氧后神经元生存率随着时间推移降低,但绝大部分神经元仍存活;CYGB核酸及蛋白的表达随缺氧时间增长而递增,且每组之间差异有统计学意义(P〈0.05)。结论在体外培养的神经元细胞中,缺氧可以促进CYGB的表达,提示CYGB在缺氧性神经损伤中可能发挥某种特定的生理功能。Objective To examine the expression of eytoglobin(CYGB) of neurons in vitro when suffered hypoxia,which provides an experimental basis for exploring the physiological and pathological mechanism and seeking new treatmentsof hypoxic-ischemic encephalopathy, methods The primary cortical neurons from embryonic rat were cultured in a serum-free culture system of B27-supplemented neurobasal medium. The neurons were identified by polyclonal antibody againstneuron specific enolase(NSE) on the 6th day. They were divided into 4 groups randomly for assessing cell viability by CCK8and observing the expression of CYGB by Real-time PCR and Westernblot at 0,8,16,24 h after hypoxic model(oxygen con-centration between 0.5%and 0.9 %) was induced, results The purity of neurons was greater than 99% ;and cell viabilitywere slightly reduced after hypoxia. Expression of RNA and protein of CYGB was increased in a time-dependent manner.And there was statistical, differenc in each group (P〈0.05). conclusions CYGI3 can up regulate in neurons in vitro afterhypoxia,indicating CYGB may play certain important roles in neurons under hypoxia.

关 键 词:细胞红蛋白 原代神经元 缺氧缺血性脑损伤 

分 类 号:Q95-33[生物学—动物学]

 

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