首页> 外文期刊>Journal of Neuropathology and Experimental Neurology >Purkinje Cell Death After Uptake of Anti-Yo Antibodies in Cerebellar Slice Cultures
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Purkinje Cell Death After Uptake of Anti-Yo Antibodies in Cerebellar Slice Cultures

机译:小脑切片培养物中摄取抗Yo抗体后浦肯野细胞死亡

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摘要

Paraneoplastic cerebellar degeneration accompanying gynecological and breast cancers is characteristically accompanied by a serum and cerebrospinal fluid (CSF) antibody response, termed "anti-Yo," which reacts with cytoplasmic proteins of cerebellar Purkinje cells. Because these antibodies interact with cytoplasmic rather than cell surface membrane proteins, their role in causing Purkinje cell death has been questioned. To address this issue, we studied the interaction of anti-Yo antibodies with Purkinje cells in slice (organotypic) cultures of rat cerebellum. We incubated cultures with immunoglobulin G (IgG)-containing anti-Yo antibodies using titers of anti-Yo antibody equivalent to those found in CSF of affected patients. Cultures were then studied in real time and after fixation for potential uptake of antibody and induction of cell death. Anti-Yo antibodies delivered in serum, CSF, or purified IgG were taken up by viable Purkinje cells, accumulated intracellularly, and were associated with cell death. Normal IgG was also taken up by Purkinje cells but did not accumulate and did not affect cell viability. These findings indicate that autoantibodies directed against intracellular Purkinje cell proteins can be taken up to cause cell death and suggest that anti-Yo antibody may be directly involved in the pathogenesis of paraneoplastic cerebellar degeneration.
机译:伴随妇科和乳腺癌的副肿瘤小脑变性通常伴随着血清和脑脊髓液(CSF)抗体反应,称为“抗-Yo”,它与小脑浦肯野细胞的胞质蛋白发生反应。由于这些抗体与细胞质而非细胞表面膜蛋白相互作用,因此它们在引起浦肯野细胞死亡中的作用受到质疑。为了解决这个问题,我们在大鼠小脑的切片(有机型)培养物中研究了抗Yo抗体与浦肯野细胞的相互作用。我们使用与感染患者脑脊液中发现的抗Yo抗体效价相等的抗体,将含有免疫球蛋白G(IgG)的抗Yo抗体孵育。然后对培养物进行实时研究,并在固定后对抗体的潜在摄取和细胞死亡的诱导进行研究。血清,CSF或纯化的IgG中递送的抗Yo抗体被存活的Purkinje细胞吸收,在细胞内积累,并与细胞死亡相关。正常的IgG也被浦肯野细胞吸收,但是没有积累并且不影响细胞活力。这些发现表明,针对细胞内浦肯野细胞蛋白的自身抗体可以被吸收以引起细胞死亡,并且表明抗Yo抗体可能直接参与副肿瘤性小脑变性的发病机理。

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    《Journal of Neuropathology and Experimental Neurology》 |2010年第10期|p.997-1007|共11页
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    John E. Greenlee, MD, Susan A. Clawson, BS, Kenneth E. Hill, MS, Blair L. Wood, BS, Ikuo Tsunoda, MD, PhD, and Noel G. Carlson, PhDFrom the Neurology Service (JEG), Research Service (NGC), and GRECC (NGC), George E. Wahlen Veterans Affairs Medical Center, the Departments of Neurology (JEG, NGC, SAC, KEH, BLW). Neurobiology and Anatomy (NGC), Center on Aging (NGC), and Brain Research Institute (JEG, NGC), University of Utah School of Medicine, Salt Lake City. Utah, and Department of Microbiology and Immunology (IT), Louisiana State University Health Sciences Center, Shreveport, Louisiana.Send correspondence and reprint requests to: John E. Greenlee, MD, Neurology Service (127), Veterans Affairs Medical Center, 500 Foothill Dr. Salt Lake City, UT 84148, E-mail: john.greenlee@hsc.utah.eduThis work was supported by a Merit Review Award from the United States Department of Veterans Affairs (Dr Greenlee) and an award from the Western Institute for Biomedical Research (Dr Greenlee). Dr Tsunoda is supported by an R21 award (R21NS059724) from the National Institutes of Health.,;

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