首页> 外文学位 >Postmitochondrial regulation of apoptosis in neurons and cancer cells.
【24h】

Postmitochondrial regulation of apoptosis in neurons and cancer cells.

机译:线粒体后调节神经元和癌细胞的凋亡。

获取原文
获取原文并翻译 | 示例

摘要

The apoptotic pathway is a genetically conserved, energetic process that is essential for the development and homeostasis of organisms. Aberrant apoptosis, however, can result in variety of diseases including neurodegeneration and cancer. Apoptotic stimuli ultimately converge at the mitochondria, where cytochrome c is released into the cytosol to trigger formation of the apoptosome complex. The active apoptosome then goes on to activate the caspase family of proteases which cleave a myriad of substrates, resulting in cell death.; The core apoptotic components are ubiquitously expressed in cells, however some cell types (such as neurons and cancer cells) have an increased need to strictly regulate the apoptotic pathway. Unlike normal mitotic cells, postmitotic neurons have little regenerative potential and must often last the lifetime of the organism. Here, I identify novel ways in which neurons and cancer cells inhibit the apoptotic pathway at points downstream of cytochrome c. Specifically, I describe mechanisms by which postmitotic neurons of the PNS and CNS posttranslationally inactivate cytochrome c and Apaf-1, respectively, in order to ensure their longterm survival. In addition, my work suggests that cancer cells may use mechanisms similar to those adapted by neurons in order to evade apoptosis.; Despite a neuron's ability to inhibit programmed cell death, these cells must still be able engage the apoptotic pathway during development or in the event of extreme stress. Here, I uncover the mechanism by which cytochrome c becomes reactivated in sympathetic neurons during developmental apoptosis. In addition, I examine how XIAP's inhibition of caspases is overcome to allow neuronal apoptosis in response to DNA damage.; Together, these results not only illustrate the importance of a strict regulation of apoptosis in differentiating neurons, but also identify the mechanisms by which these blocks are overcome to allow death. I hope that a deeper knowledge of how the apoptotic pathway is reactivated in dying neurons could eventually lead to therapeutics to inhibit cell death in the context of neuronal pathologies, or to promote cell death in cancer.
机译:凋亡途径是遗传保守的,充满活力的过程,对生物体的发育和体内平衡至关重要。然而,异常的细胞凋亡可导致多种疾病,包括神经变性和癌症。细胞凋亡的刺激最终汇聚于线粒体,在那里细胞色素c被释放到细胞质中,触发凋亡小体复合物的形成。然后,有活性的凋亡小体继续激活蛋白酶的胱天蛋白酶家族,该蛋白酶裂解无数种底物,导致细胞死亡。核心凋亡成分在细胞中普遍表达,但是某些细胞类型(例如神经元和癌细胞)对严格调控凋亡途径的需求增加。与正常的有丝分裂细胞不同,有丝分裂后的神经元几乎没有再生潜能,并且必须经常持续存在。在这里,我确定了神经元和癌细胞在细胞色素c下游点抑制凋亡途径的新途径。具体来说,我描述了PNS和CNS的有丝分裂后神经元分别翻译后灭活细胞色素c和Apaf-1的机制,以确保它们的长期存活。另外,我的工作表明癌细胞可以利用类似于神经元适应的机制来逃避凋亡。尽管神经元具有抑制程序性细胞死亡的能力,但这些细胞仍必须能够在发育过程中或在极度应激的情况下参与凋亡途径。在这里,我揭示了在细胞凋亡过程中交感神经元中细胞色素c重新活化的机制。此外,我研究了如何克服XIAP对胱天蛋白酶的抑制作用,以使神经元凋亡响应DNA损伤。总之,这些结果不仅说明了在分化神经元中严格调控细胞凋亡的重要性,而且还确定了克服这些障碍而导致死亡的机制。我希望对垂死的神经元中的凋亡途径如何重新激活有更深入的了解,最终可以导致在神经元病理学背景下抑制细胞死亡或促进癌症中细胞死亡的治疗方法。

著录项

  • 作者

    Vaughn, Allyson Evans.;

  • 作者单位

    The University of North Carolina at Chapel Hill.$bCell & Developmental Biology.;

  • 授予单位 The University of North Carolina at Chapel Hill.$bCell & Developmental Biology.;
  • 学科 Biology Neuroscience.; Biology Cell.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 209 p.
  • 总页数 209
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经科学;细胞生物学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号