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在实验性自身免疫性神经炎中,巨噬细胞而非施万细胞表达Ia抗原。

Macrophages but not Schwann cells express Ia antigen in experimental autoimmune neuritis.

作者信息

Schmidt B, Stoll G, Hartung H P, Heininger K, Schäfer B, Toyka K V

机构信息

Department of Neurology, University of Düsseldorf, West Germany.

出版信息

Ann Neurol. 1990 Jul;28(1):70-7. doi: 10.1002/ana.410280113.

Abstract

This study was designed to identify which cells express major histocompatibility complex class II (Ia) antigen in experimental autoimmune neuritis and may therefore be antigen presenters. Serial 1-micron-thick cryosections of ventral roots of animals with experimental autoimmune neuritis were labeled with Ox6 antibody against rat Ia, the ED1 antibody to identify monocytes/macrophages and an antiserum against S100, a marker for Schwann cells. Ia-positive cells were predominantly present before overt clinical signs and demyelination (day 12). At later stages when many axons were demyelinated, their number was markedly reduced. Few Ia-positive cells that had extending long processes, which over some distance were in immediate contact with several myelin sheaths, were scattered in normal-appearing nerve roots at these later time points. Most of the Ia-positive cells could be identified as ED1-positive lean monocytes/macrophages, but in contrast most phagocytic macrophages in advanced stages of myelin degradation no longer expressed Ia. Ia-positive structures were invariably negative for S100 at early and late stages of experimental autoimmune neuritis, indicating that Schwann cells did not express identifiable Ia antigen. These findings contrast with reports of expression of major histocompatibility complex class II antigens by Schwann cells in human neuropathies. Furthermore they do not support the notion that aberrant Ia expression by Schwann cells plays a major pathogenic role in experimental autoimmune disease of the peripheral nervous system.

摘要

本研究旨在确定在实验性自身免疫性神经炎中哪些细胞表达主要组织相容性复合体II类(Ia)抗原,因此可能是抗原呈递细胞。用抗大鼠Ia的Ox6抗体、用于识别单核细胞/巨噬细胞的ED1抗体以及针对雪旺细胞标志物S100的抗血清,对患有实验性自身免疫性神经炎动物的腹侧神经根连续1微米厚的冰冻切片进行标记。Ia阳性细胞主要在明显的临床症状和脱髓鞘出现之前(第12天)就已存在。在许多轴突发生脱髓鞘的后期阶段,它们的数量明显减少。在这些后期时间点,少数具有延伸长突起且在一定距离内与多个髓鞘直接接触的Ia阳性细胞散在于外观正常的神经根中。大多数Ia阳性细胞可被鉴定为ED1阳性的瘦单核细胞/巨噬细胞,但相比之下,在髓鞘降解晚期的大多数吞噬性巨噬细胞不再表达Ia。在实验性自身免疫性神经炎的早期和晚期,Ia阳性结构对S100始终呈阴性,表明雪旺细胞不表达可识别 的Ia抗原。这些发现与人类神经病变中雪旺细胞表达主要组织相容性复合体II类抗原的报道形成对比。此外,它们不支持雪旺细胞异常表达Ia在外周神经系统实验性自身免疫性疾病中起主要致病作用的观点。

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