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首页> 外文期刊>Archives of medical research >Myelin-Basic Protein-reactive Specific CD4(+) and CD8(+) NK Lymphocytes Induce Morphological Changes in Neuronal Cell Bodies and Myelin Sheaths: Implications for Multiple Sclerosis.
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Myelin-Basic Protein-reactive Specific CD4(+) and CD8(+) NK Lymphocytes Induce Morphological Changes in Neuronal Cell Bodies and Myelin Sheaths: Implications for Multiple Sclerosis.

机译:髓磷脂碱性蛋白反应性特异性CD4(+)和CD8(+)NK淋巴细胞诱导神经元细胞体和髓鞘的形态变化:对多发性硬化症的影响。

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摘要

BACKGROUND: Multiple sclerosis (MS) is a chronic disease characterized by loss of myelin. However, data indicate that autoimmune cells could directly impair neuronal cell bodies and myelin sheath is lacking. The aim of the present study was to determine morphological evidence of the direct impairment of neurons by autoreactive lymphocytes and to further identify the subtypes of these lymphocytes. METHODS: Lymphocytes activated by myelin basic protein (MBP) 83-99 and neurons of human brain were co-cultured for 24 h. RESULTS: Observations through scanning electron microscope showed that MBP-specific lymphocytes (CD4+, CD8+ cells, and NK cells) aggregated in the vicinity of the neuronal cell bodies and the myelin sheaths and attacked them directly, resulting in the degeneration of both neurons. CONCLUSIONS: Our studies provide morphological evidences of the direct impairment of neuronal cell bodies and myelin sheaths by MBP-specific lymphocytes. Our studies also suggest that MBP-specific CD4+, CD8+, and NK cells might be involved in this process. These processes may play a role in the direct impairment of neurons and myelin sheaths in early stages of MS and provide evidences for the application of immunosuppressant therapy of MS.
机译:背景:多发性硬化症(MS)是一种以髓磷脂减少为特征的慢性疾病。然而,数据表明自身免疫细胞可直接损害神经元细胞体,而缺乏髓鞘。本研究的目的是确定自身反应性淋巴细胞直接损伤神经元的形态学证据,并进一步鉴定这些淋巴细胞的亚型。方法:将髓磷脂碱性蛋白(MBP)83-99激活的淋巴细胞与人脑神经元共培养24 h。结果:通过扫描电子显微镜观察,MBP特异性淋巴细胞(CD4 +,CD8 +和NK细胞)聚集在神经元细胞体和髓鞘附近,并直接攻击它们,导致两个神经元变性。结论:我们的研究提供了MBP特异性淋巴细胞直接损伤神经元细胞体和髓鞘的形态学证据。我们的研究还表明,MBP特异性CD4 +,CD8 +和NK细胞可能参与此过程。这些过程可能在MS的早期阶段直接损害神经元和髓鞘,并为MS的免疫抑制剂治疗的应用提供证据。

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