{"title":"[Heat shock proteins in diabetes mellitus].","authors":"C Parlapiano,&nbsp;E Campana,&nbsp;C Rota,&nbsp;E Vecci","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The Heat Shock Proteins (HSP) are a special category of proteins synthesized from 2 types of cells, one originating from ordinary organs and the other highly specialized ones from mammals. Their synthesis originates from a reaction of the cells to heat shock and therefore it can be thought of as a defense mechanism activated by the cells to protect themselves from the damage done by heat. HSPs are also qualified as \"molecular chaperons\" since they are present at the assembling of other proteins and they protect them from any possible anomalous interactions even if they do not take an active part in the final making up of the protein itself. This chaperone role is the base of the hypothesis that HSPs could take part in the processing and presentation of the antigens. Two hypothesis have been formed on the role of HSPs in the immunological process. 1) HSP could be antigens that call for an immediate immunological reaction; 2) HSP could set off a self destructive mechanism brought on by an immunological reaction. From all this it emerges that the immunological reaction to HSP has two angles. One is protective in that it allows the cells to eliminate micro foreign-organisms and the other is harmful due to a badly regulated immunological reaction. In some studies it has been demonstrated that patients with varying autoimmunological disorders as LES and rheumatoid arthritis (AR), have autoantibodies against HSPs. Moreover the HSPs of certain microorganisms induce the formation of autoantibodies in the host and the proliferation of T cells in the synovial fluid in patients with AR.(ABSTRACT TRUNCATED AT 250 WORDS)</p>","PeriodicalId":21382,"journal":{"name":"Rivista europea per le scienze mediche e farmacologiche = European review for medical and pharmacological sciences = Revue europeenne pour les sciences medicales et pharmacologiques","volume":"17 1","pages":"27-33"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rivista europea per le scienze mediche e farmacologiche = European review for medical and pharmacological sciences = Revue europeenne pour les sciences medicales et pharmacologiques","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

The Heat Shock Proteins (HSP) are a special category of proteins synthesized from 2 types of cells, one originating from ordinary organs and the other highly specialized ones from mammals. Their synthesis originates from a reaction of the cells to heat shock and therefore it can be thought of as a defense mechanism activated by the cells to protect themselves from the damage done by heat. HSPs are also qualified as "molecular chaperons" since they are present at the assembling of other proteins and they protect them from any possible anomalous interactions even if they do not take an active part in the final making up of the protein itself. This chaperone role is the base of the hypothesis that HSPs could take part in the processing and presentation of the antigens. Two hypothesis have been formed on the role of HSPs in the immunological process. 1) HSP could be antigens that call for an immediate immunological reaction; 2) HSP could set off a self destructive mechanism brought on by an immunological reaction. From all this it emerges that the immunological reaction to HSP has two angles. One is protective in that it allows the cells to eliminate micro foreign-organisms and the other is harmful due to a badly regulated immunological reaction. In some studies it has been demonstrated that patients with varying autoimmunological disorders as LES and rheumatoid arthritis (AR), have autoantibodies against HSPs. Moreover the HSPs of certain microorganisms induce the formation of autoantibodies in the host and the proliferation of T cells in the synovial fluid in patients with AR.(ABSTRACT TRUNCATED AT 250 WORDS)

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[糖尿病热休克蛋白]。
热休克蛋白(HSP)是由两种细胞合成的一类特殊蛋白质,一种来自普通器官,另一种来自哺乳动物的高度特化的细胞。它们的合成源于细胞对热休克的反应,因此它可以被认为是细胞激活的一种防御机制,以保护自己免受热造成的伤害。热休克蛋白也被称为“分子伴侣”,因为它们存在于其他蛋白质的组装中,即使它们在蛋白质本身的最终组成中没有积极的参与,它们也可以保护蛋白质免受任何可能的异常相互作用。这种伴侣作用是热敏感蛋白可能参与抗原加工和呈递的假设的基础。关于热休克蛋白在免疫过程中的作用,目前形成了两种假说。1)热休克蛋白可能是引起立即免疫反应的抗原;2)热休克蛋白可触发免疫反应引起的自毁机制。由此可见,对热休克蛋白的免疫反应有两个角度。一种是保护性的,因为它允许细胞消除外来微生物,另一种是有害的,因为免疫反应受到严重调节。在一些研究中,已经证明患有各种自身免疫性疾病如LES和类风湿关节炎(AR)的患者具有针对热休克蛋白的自身抗体。此外,某些微生物的热休克蛋白诱导宿主体内自身抗体的形成和AR患者滑液中T细胞的增殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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