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王广雷, 黄国伟, 张绪梅, 丛革新, 姬长珍, 田志红. 叶酸对胎鼠大脑神经干细胞增殖蛋白表达影响[J]. 中国公共卫生, 2008, 24(4): 462-464. DOI: 10.11847/zgggws2008-24-04-47
引用本文: 王广雷, 黄国伟, 张绪梅, 丛革新, 姬长珍, 田志红. 叶酸对胎鼠大脑神经干细胞增殖蛋白表达影响[J]. 中国公共卫生, 2008, 24(4): 462-464. DOI: 10.11847/zgggws2008-24-04-47
WANG Guang-lei, HUANG Guo-wei, ZHANG Xu-mei, . Effects of folate on proliferation of neural stem cells of fetal rat[J]. Chinese Journal of Public Health, 2008, 24(4): 462-464. DOI: 10.11847/zgggws2008-24-04-47
Citation: WANG Guang-lei, HUANG Guo-wei, ZHANG Xu-mei, . Effects of folate on proliferation of neural stem cells of fetal rat[J]. Chinese Journal of Public Health, 2008, 24(4): 462-464. DOI: 10.11847/zgggws2008-24-04-47

叶酸对胎鼠大脑神经干细胞增殖蛋白表达影响

Effects of folate on proliferation of neural stem cells of fetal rat

  • 摘要: 目的 研究叶酸对胎鼠大脑神经干细胞(NSCs)增殖的影响及其作用机制。方法 采用孕14~16 d SD胎鼠,进行NSCs原代培养。将NSCs分为4组:对照组、叶酸缺乏组、叶酸低剂量组、叶酸高剂量组。收集培养6 d的细胞,采用5-溴脱氧尿苷(BrdU)掺入法和免疫组化双标记检测NSCs的增殖情况,采用蛋白印迹法(Western blot)检测胎鼠增殖期NSCs活化的细胞外信号调节激酶1/2(pERK1/2)的表达含量。结果 叶酸低剂量组、高剂量组BrdU+巢蛋白(Nestin)阳性细胞占总细胞(70.5±2.7),(78.8±6.9)%与对照组(64.2±8.9)%比较,差异均有统计学意义,且高剂量组明显高于低剂量组(P<0.05);叶酸低剂量组、高剂量组pERK1蛋白的表达(0.407±0.018),(0.443±0.019)与对照组(0.388±0.011)比较,差异均有统计学意义(P<0.05)。叶酸低剂量组、高剂量组pERK2蛋白的表达(0.547±0.044),(0.563±0.041)与对照组(0.507±0.018)比较,差异均有统计学意义(P<0.05)。结论 叶酸能够促进胎鼠NSCs的增值,其作用机制可能是通过丝裂原活化蛋白激酶信号通路调节NSCs的增殖。

     

    Abstract: Objective To study the effect of folate on neural stem cells(NSCs)proliferation via MARK signal pathway in fetal rats in vitro.Methods NSCs of fetal Sprague-Dawley rat from E14d to E16d were cultured,divided into four groups which were control group,folate-deficiency group,folate-low group and folate-high group.NSCs were collected after being cultrured 6 d.The proliferation of NSCs was detected by BrdU in corporating method and immunohistochemistry method.The level of pERK1/2 expression were detected by western blot method.Results The percentage of Nestin and BrdU positive cells in total cells(x±s)in folate-low group(70.5±2.7)and folate-high group(78.8±6.9)was significantly higher than that in control group((64.2±8.9),P<0.05).The levels of pERK1(x±s)in folate-low group(0.407 ±0.018)and folate-high group(01443±01019)were higher than those in control group((0.388±0.011),P<0.05),and the levels of pERK2 in folate-low group(0.547±0.044)and folate-high group(0.563±0.041)were higher than those in control group((0.507±0.018),P<0.05).Conclusion Folate could promote proliferation of fetal NSCs via MAPK signal pathway.

     

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