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实验性自身免疫性脑脊髓炎中枢神经系统中的巨噬细胞凋亡

Macrophage apoptosis in the central nervous system in experimental autoimmune encephalomyelitis.

作者信息

Nguyen K B, McCombe P A, Pender M P

机构信息

Department of Medicine, University of Queensland, Royal Brisbane Hospital, Australia.

出版信息

J Autoimmun. 1994 Apr;7(2):145-52. doi: 10.1006/jaut.1994.1011.

Abstract

Using light and electron microscopy, we have demonstrated that macrophage apoptosis (programmed cell death) occurs in the central nervous system (CNS) in Lewis rats with acute experimental autoimmune encephalomyelitis (EAE) and chronic relapsing EAE. Apoptotic macrophages were identified by the presence of an apoptotic nucleus in a cell with cytoplasm containing myelin debris but no intermediate filaments. They were found in the meninges, perivascular spaces and in the parenchyma of the white and grey matter of the spinal cord. In acute EAE the apoptotic macrophages were most frequently seen at the time of maximal neurological signs and during the early stages of clinical recovery. Several possible mechanisms may be responsible for the macrophage apoptosis: the release or withdrawal of cytokines; T-cell cytotoxicity; the effect of activated macrophage products, such as nitric oxide; and a direct effect of endogenous glucocorticoids. Macrophage apoptosis, together with the T-cell apoptosis we have previously described in the CNS in EAE, may contribute to the down-regulation of this autoimmune disease.

摘要

利用光学显微镜和电子显微镜,我们已经证明,在患有急性实验性自身免疫性脑脊髓炎(EAE)和慢性复发性EAE的Lewis大鼠的中枢神经系统(CNS)中,巨噬细胞凋亡(程序性细胞死亡)会发生。通过在一个细胞质中含有髓磷脂碎片但没有中间丝的细胞中存在凋亡核来鉴定凋亡巨噬细胞。它们存在于脊髓白质和灰质的脑膜、血管周围间隙以及实质中。在急性EAE中,凋亡巨噬细胞最常见于神经症状最严重时以及临床恢复的早期阶段。巨噬细胞凋亡可能有几种可能的机制:细胞因子的释放或撤离;T细胞细胞毒性;活化巨噬细胞产物(如一氧化氮)的作用;以及内源性糖皮质激素的直接作用。巨噬细胞凋亡,连同我们之前在EAE的中枢神经系统中描述的T细胞凋亡,可能有助于下调这种自身免疫性疾病。

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