Suppr超能文献

促凋亡蛋白ARTS/Sept4在精神分裂症患者的尸检大脑中显著减少。

The pro-apoptotic ARTS/Sept4 protein is significantly reduced in post-mortem brains from schizophrenic patients.

作者信息

Gottfried Yossi, Rotem Asaf, Klein Ehud, Larisch Sarit

机构信息

Apoptosis and Cancer Research Laboratory, Pathology Department, Rambam Medical Center and Faculty of Medicine, Technion, Haifa, Israel.

出版信息

Schizophr Res. 2007 Nov;96(1-3):257-66. doi: 10.1016/j.schres.2007.05.031. Epub 2007 Jul 17.

Abstract

Schizophrenic brains exhibit various neuro-pathological changes in size, volume and structure as compared to normal brains. These structural abnormalities could be the result of apoptotic cell death. ARTS/Sept4 protein plays an important role in induction and promotion of apoptosis. Though ARTS is highly expressed in the healthy human brain, most of tested schizophrenic brain samples showed no expression of ARTS protein. Specifically, using Western blot analysis with monoclonal anti-ARTS antibody we found that only 1 out of 14 schizophrenic samples (7%) showed a strong ARTS signal as compared to 10 out of 15 (66.6%) found in the normal controls group. Furthermore, using immunohistochemistry assay only 33.3% (5 of 15) (SE+/-12.5) of the schizophrenic patients samples showed any ARTS immunoreactivity as compared to (13 of 15) 87% (SE+/-9) of bipolar, (11 of 14) 78% (SE+/-11.3) of major depression and (10 of 14) 71% (SE+/-12.5) of normal controls. A four-fold reduction in apoptosis rate was measured in these schizophrenic samples as compared to average apoptosis rate found in all other samples. These data support the linkage between loss of ARTS expression and the loss of sensitivity towards apoptosis. Interestingly, levels of ARTS were significantly lower in male schizophrenic patients as compared to female schizophrenic patients, and males of all other control groups. We propose that ARTS may play an important role in the pathogenesis of schizophrenia and could be used as a marker for this disease.

摘要

与正常大脑相比,精神分裂症患者的大脑在大小、体积和结构上表现出各种神经病理学变化。这些结构异常可能是细胞凋亡性死亡的结果。ARTS/Sept4蛋白在诱导和促进细胞凋亡中起重要作用。尽管ARTS在健康人脑中高度表达,但大多数测试的精神分裂症脑样本显示无ARTS蛋白表达。具体而言,使用单克隆抗ARTS抗体进行蛋白质印迹分析,我们发现14个精神分裂症样本中只有1个(7%)显示出强烈的ARTS信号,而正常对照组的15个样本中有10个(66.6%)显示出该信号。此外,使用免疫组织化学分析,只有33.3%(15个样本中的5个)(标准误±12.5)的精神分裂症患者样本显示出任何ARTS免疫反应性,相比之下,双相情感障碍患者样本中有87%(15个样本中的13个)(标准误±9)、重度抑郁症患者样本中有78%(14个样本中的11个)(标准误±11.3)、正常对照组样本中有71%(14个样本中的10个)(标准误±12.5)显示出该反应性。与所有其他样本的平均凋亡率相比,这些精神分裂症样本的凋亡率降低了四倍。这些数据支持ARTS表达缺失与对细胞凋亡敏感性丧失之间的联系。有趣的是,与女性精神分裂症患者以及所有其他对照组的男性相比,男性精神分裂症患者的ARTS水平显著较低。我们认为,ARTS可能在精神分裂症的发病机制中起重要作用,并可作为该疾病的一个标志物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验