首页> 外文期刊>Neurochemical research >Spatiotemporal Expression of Bcl-2/Bax and Neural Cell Apoptosis in the Developing Lumbosacral Spinal Cord of Rat Fetuses with Anorectal Malformations
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Spatiotemporal Expression of Bcl-2/Bax and Neural Cell Apoptosis in the Developing Lumbosacral Spinal Cord of Rat Fetuses with Anorectal Malformations

机译:Bcl-2 / Bax和神经细胞凋亡的时尚表达在大鼠胎儿椎间盘胸腔脊髓中具有肛门直肠畸形

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Abstract Fecal incontinence and constipation still remain the major complications after procedures for anorectal malformations (ARMs). Previous studies have demonstrated a decrease of neural cell in lumbosacral spinal cord of ARMs patients and rat models. However, the underlying mechanism remains elusive. In this study, the neural cell apoptosis and Bcl-2/Bax expression were explored during lumbosacral spinal cord development in normal and ARMs fetuses. ARMs rat fetuses were induced by treating pregnant rats with ethylenethiourea on embryonic day 10. TUNEL staining was performed to identify apoptosis, and the expression of Bcl-2/Bax was confirmed with immunohistochemical staining, RT-qPCR and Western blot analysis on E16, E17, E19 and E21. Apoptosis index (AI) in the ARMs group was significantly higher compared to normal group. Our results showed that TUNEL-positive cells were mainly localized in the ventral horn, which is the location of neural cells controlling defecation. And the expression of Bcl-2 decreased, whereas the level of Bax increased in the ARMs fetuses. In addition, there was a significantly negative correlation between protein expression of Bcl-2/Bax ratio and AI in the ARMs group. Abnormal apoptosis might be a fundamental pathogenesis for the number decrease of neural cells in lumbosacral spinal cord, which leads to complications after procedures for ARMs. The negative correlation between the ratio of Bcl-2/Bax and AI manifested that Bcl-2/Bax pathway might be the mechanism for neural cell apoptosis in ARMs.
机译:摘要粪便尿失禁和便秘仍然是肛门畸形(手臂)的程序后的主要并发症。以前的研究表明,腰骶脊髓脊髓脊髓脊髓和大鼠模型的脊髓神经细胞减少。然而,潜在机制仍然难以捉摸。在该研究中,在正常和臂胎儿的腰骶部脊髓发育过程中探讨了神经细胞凋亡和Bcl-2 / Bax表达。通过在胚胎第10天用乙烯乙烯脲处理妊娠大鼠诱导靶血管诱导。进行TUNEL染色以鉴定细胞凋亡,并用免疫组织化学染色,RT-QPCR和E17的Western印迹分析证实Bcl-2 / Bax的表达。 ,E19和E21。与正常组相比,臂组中的凋亡指数(AI)显着高。我们的研究结果表明,TUNEL阳性细胞主要是腹侧喇叭,这是控制排便的神经细胞的位置。并且Bcl-2的表达降低,而Bax的水平增加在臂胎儿中。此外,在臂组中的Bcl-2 / Bax比率和Ai的蛋白质表达与Ai之间存在显着的负相关性。异常细胞凋亡可能是腰骶部脊髓神经细胞数量减少的根本发病机制,导致武器程序后的并发症。 BCL-2 / BAX和AI比之间的负相关性表现为BCL-2 / BAX途径可能是臂中神经细胞凋亡的机制。

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