首页> 美国卫生研究院文献>other >Anti-Yo Antibody Uptake and Interaction with Its Intracellular Target Antigen Causes Purkinje Cell Death in Rat Cerebellar Slice Cultures: A Possible Mechanism for Paraneoplastic Cerebellar Degeneration in Humans with Gynecological or Breast Cancers
【2h】

Anti-Yo Antibody Uptake and Interaction with Its Intracellular Target Antigen Causes Purkinje Cell Death in Rat Cerebellar Slice Cultures: A Possible Mechanism for Paraneoplastic Cerebellar Degeneration in Humans with Gynecological or Breast Cancers

机译:抗Yo抗体的摄取及其与细胞内靶抗原的相互作用导致大鼠小脑切片培养物中的浦肯野细胞死亡:妇科或乳腺癌患者副肿瘤小脑变性的可能机制

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Anti-Yo antibodies are immunoglobulin G (IgG) autoantibodies reactive with a 62 kDa Purkinje cell cytoplasmic protein. These antibodies are closely associated with paraneoplastic cerebellar degeneration in the setting of gynecological and breast malignancies. We have previously demonstrated that incubation of rat cerebellar slice cultures with patient sera and cerebrospinal fluid containing anti-Yo antibodies resulted in Purkinje cell death. The present study addressed three fundamental questions regarding the role of anti-Yo antibodies in disease pathogenesis: 1) Whether the Purkinje cell cytotoxicity required binding of anti-Yo antibody to its intraneuronal 62 kDa target antigen; 2) whether Purkinje cell death might be initiated by antibody-dependent cellular cytotoxicity rather than intracellular antibody binding; and 3) whether Purkinje cell death might simply be a more general result of intracellular antibody accumulation, rather than of specific antibody-antigen interaction. In our study, incubation of rat cerebellar slice cultures with anti-Yo IgG resulted in intracellular antibody binding, and cell death. Infiltration of the Purkinje cell layer by cells of macrophage/microglia lineage was not observed until extensive cell death was already present. Adsorption of anti-Yo IgG with its 62 kDa target antigen abolished both antibody accumulation and cytotoxicity. Antibodies to other intracellular Purkinje cell proteins were also taken up by Purkinje cells and accumulated intracellularly; these included calbindin, calmodulin, PCP-2, and patient anti-Purkinje cell antibodies not reactive with the 62 kDa Yo antigen. However, intracellular accumulation of these antibodies did not affect Purkinje cell viability. The present study is the first to demonstrate that anti-Yo antibodies cause Purkinje cell death by binding to the intracellular 62 kDa Yo antigen. Anti-Yo antibody cytotoxicity did not involve other antibodies or factors present in patient serum and was not initiated by brain mononuclear cells. Purkinje cell death was not simply due to intraneuronal antibody accumulation.
机译:抗-Yo抗体是与62 kDa浦肯野细胞胞浆蛋白发生反应的免疫球蛋白G(IgG)自身抗体。这些抗体在妇科和乳腺恶性肿瘤的发生中与副肿瘤小脑变性密切相关。我们以前已经证明,将大鼠小脑切片培养物与患者血清和含有抗Yo抗体的脑脊髓液一起孵育会导致浦肯野细胞死亡。本研究解决了有关抗-Yo抗体在疾病发病机理中的作用的三个基本问题:1)浦肯野细胞的细胞毒性是否需要抗-Yo抗体与其神经内62 kDa靶抗原的结合; 2)浦肯野细胞死亡是否可能由抗体依赖性细胞毒性而不是细胞内抗体结合引起; 3)浦肯野细胞的死亡是否可能仅仅是细胞内抗体积累而不是特异性抗体-抗原相互作用的更普遍的结果。在我们的研究中,将大鼠小脑切片培养物与抗Yo IgG一起孵育会导致细胞内抗体结合和细胞死亡。巨噬细胞/小胶质细胞系细胞未观察到浦肯野细胞层的浸润,直到已经存在广泛的细胞死亡。抗-Yo IgG及其62 kDa靶抗原的吸附消除了抗体积聚和细胞毒性。其他细胞内浦肯野细胞蛋白的抗体也被浦肯野细胞吸收并在细胞内积累。这些包括钙调蛋白,钙调蛋白,PCP-2和与62 kDa Yo抗原不反应的患者抗Purkinje细胞抗体。但是,这些抗体在细胞内的积累并不影响浦肯野细胞的生存能力。本研究是第一个证明抗Yo抗体通过结合细胞内62 kDa Yo抗原引起浦肯野细胞死亡的研究。抗Yo抗体的细胞毒性不涉及患者血清中存在的其他抗体或因子,也不是由脑单核细胞引发的。浦肯野细胞的死亡不仅仅是由于神经内抗体的积累。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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