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维甲酸诱导的大鼠开放性脊柱裂腰骶神经管发育中神经上皮细胞凋亡和增殖紊乱。

Disturbed apoptosis and cell proliferation in developing neuroepithelium of lumbo-sacral neural tubes in retinoic acid-induced spina bifida aperta in rat.

作者信息

Wei Xiaowei, Li Hui, Miao Jianing, Zhou Fenghua, Liu Bo, Wu Di, Li Shujing, Wang Lili, Fan Yang, Wang Weilin, Yuan Zhengwei

机构信息

Key Laboratory of Health Ministry for Congenital Malformation, Shengjing Hospital, China Medical University, Shenyang, China.

出版信息

Int J Dev Neurosci. 2012 Aug;30(5):375-81. doi: 10.1016/j.ijdevneu.2012.03.340. Epub 2012 Apr 5.

Abstract

Spina bifida is a complex congenital malformation resulting from failure of fusion in the spinal neural tube during embryogenesis. However, the cellular mechanism underlying spina bifida is not fully understood. Here, we investigated cell apoptosis in whole embryos and proliferation of neural progenitor cells in the spinal neural tube during neurulation in all-trans retinoic acid (atRA)-induced spina bifida in fetal rats. Cell apoptosis was assessed by TUNEL assay on whole-mount and serially sectioned samples of rat embryos with spina bifida. Cell proliferation of lumbo-sacral neural progenitor cells was assessed by staining for the mitotic marker Ki67 and pH3. We found an excess of apoptosis in the neuroepithelium of embryos with spina bifida, which became more marked as embryos progress from E11 to E13. Conversely, there was a reduction in cell proliferation in spina bifida embryos, with a progressively greater difference from controls with stage from E11 to 13. Thus, atRA-induced spina bifida in rat shows perturbed apoptosis and proliferation of neural progenitors in the lumbo-sacral spinal cord during embryonic development, which might contribute to the pathogenesis of spina bifida.

摘要

脊柱裂是一种复杂的先天性畸形,由胚胎发育过程中脊髓神经管融合失败所致。然而,脊柱裂潜在的细胞机制尚未完全明确。在此,我们研究了全反式维甲酸(atRA)诱导的胎鼠脊柱裂在神经胚形成过程中全胚胎的细胞凋亡以及脊髓神经管中神经祖细胞的增殖情况。通过对患有脊柱裂的大鼠胚胎的整体标本和连续切片样本进行TUNEL检测来评估细胞凋亡。通过对有丝分裂标记物Ki67和pH3进行染色来评估腰骶部神经祖细胞的细胞增殖。我们发现患有脊柱裂的胚胎神经上皮细胞凋亡过多,随着胚胎从E11发育到E13,这种情况变得更加明显。相反,脊柱裂胚胎中的细胞增殖减少,从E11到E13,与对照组相比差异逐渐增大。因此,atRA诱导的大鼠脊柱裂在胚胎发育过程中显示出腰骶部脊髓神经祖细胞凋亡和增殖紊乱,这可能有助于脊柱裂的发病机制。

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