
脐血单个核细胞侧脑室移植对HIBD新生大鼠脑神经元凋亡及Bax、Bcl-2蛋白的影响
闫少珍, 王晓莉, 王海宇, 董鹏, 赵岩松
中国当代儿科杂志 ›› 2016, Vol. 18 ›› Issue (9) : 862-866.
脐血单个核细胞侧脑室移植对HIBD新生大鼠脑神经元凋亡及Bax、Bcl-2蛋白的影响
Effects of umbilical cord blood mononuclear cells transplantation via lateral ventricle on the neural apoptosis and the expression of Bax and Bcl-2 proteins in neonatal rats with hypoxic-ischemic brain damage
目的 探讨脐血单个核细胞移植对缺氧缺血性脑损伤 (HIBD)新生大鼠脑神经元凋亡及Bax、Bcl-2蛋白的影响。方法 7日龄Sprague-Dawley新生大鼠制备缺氧缺血性脑损伤 (HIBD)模型,随机分为正常对照 (N)+生理盐水 (NS)、HIBD+NS、N+脐血单个核细胞 (UCBMC)及HIBD+UCBMC组。N+UCBMC与HIBD+UCBMC组侧脑室注入3×106个UCBMC,N+NS与HIBD+NS组注入等体积NS。移植后7 d采用NeuN/活性Caspase-3免疫荧光双标染色法、TUNEL法观察大脑皮层神经元凋亡,Western blot观察脑组织Bax、Bcl-2蛋白表达。结果 HIBD+NS组的NeuN+活性Caspase-3+DAPI+细胞及TUNEL+DAPI+细胞均多于N+NS和N+UCBMC组 (P < 0.01);HIBD+UCBMC组的NeuN+活性Caspase-3+DAPI+细胞及TUNEL+DAPI+细胞均少于HIBD+NS组 (P < 0.01)。HIBD+NS组的Bax蛋白表达高于N+NS与N+UCBMC组,Bcl-2蛋白低于N+NS与N+UCBMC组 (P < 0.01);而HIBD+UCBMC组的Bax蛋白较HIBD+NS组降低 (P < 0.01),Bcl-2蛋白则高于HIBD+NS组、N+NS和N+UCBMC组 (P < 0.05)。结论 HIBD新生大鼠侧脑室移植UCBMC可以减轻神经元凋亡,其机制可能与Bcl-2蛋白表达上调,Bax蛋白表达下调有关。
Objective To explore the effects of umbilical cord blood mononuclear cells (UCBMC) transplantation on the neuronal apoptosis and the expression of Bcl-2 and Bax proteins in neonatal rats with hypoxic-ischemic brain damage (HIBD). Methods Seven-day-old Sprague-Dawley neonatal rats were randomly divided into normal control (N)+normal saline (NS), HIBD+NS, N+UCBMC, and HIBD+UCBMC groups. HIBD model was prepared using the classical Rice-Vannucci method. Twenty-four hours after HIBD, UCBMC were transplanted in the N+UCBMC and HIBD+UCBMC groups. Seven days after transplantation, NeuN/Cleaved-Caspase-3 double immunofluorescence staining and TUNEL methods were used to observe neural apoptosis in the cortex. The expression levels of Bax and Bcl-2 proteins were examined by Western blot analysis. Results There were more NeuN+ cleaved Caspase-3+DAPI+ and TUNEL+DAPI+ cells in the HIBD+NS group compared with the N+NS and N+UCBMC groups (P < 0.01). There were less NeuN+ cleaved Caspase-3+DAPI+ and TUNEL+DAPI+ cells in the HIBD+UCBMC group compared with the HIBD+NS group (P < 0.01). The concentration of Bax protein was higher and that of Bcl-2 proteins was lower in the HIBD+NS group compared with the N+NS and N+UCBMC groups (P < 0.01). The concentration of Bax protein in HIBD+UCBMC group was lower than that in the HIBD+NS group (P < 0.01). The concentration of Bcl-2 protein was higher compared with the HIBD+NS, N+NS and N+UCBMC groups (P < 0.05). Conclusions UCBMC transplantation via lateral ventricle can upregulate the expression of Bcl-2 protein and down-regulate the expression of Bax protein, thus alleviating brain neural apoptosis in neonatal rats with HIBD.
脐血单个核细胞 / 缺氧缺血性脑损伤 / 凋亡 / Bax/Bcl-2 / 新生大鼠
Umbilical cord blood mononuclear cell / Hypoxic-ischemic brain damage / Apoptosis / Bax/Bcl-2 / Neonatal rats
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国家自然科学基金项目(81000268);山东省自然科学基金项目(ZR2014JL049);山东省医药卫生科技发展计划项目(2014WS0466)。