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眼眼前房同种异体排斥反应过程中细胞毒性 T 淋巴细胞功能的研究。

Investigation of Cytotoxic T Lymphocyte Function during Allorejection in the Anterior Chamber of the Eye.

机构信息

Cellular Neurophysiology, Center for Integrative Physiology and Molecular Medicine (CIPMM), Saarland University, 66421 Homburg, Germany.

出版信息

Int J Mol Sci. 2020 Jun 30;21(13):4660. doi: 10.3390/ijms21134660.

Abstract

Cytotoxic T lymphocytes (CTL) are an essential part of our immune system by killing infected and malignant cells. To fully understand this process, it is necessary to study CTL function in the physiological setting of a living organism to account for their interplay with other immune cells like CD4 T helper cells and macrophages. The anterior chamber of the eye (ACE), originally developed for diabetes research, is ideally suited for non-invasive and longitudinal in vivo imaging. We take advantage of the ACE window to observe immune responses, particularly allorejection of islets of Langerhans cells by CTLs. We follow the onset of the rejection after vascularization on islets until the end of the rejection process for about a month by repetitive two-photon microscopy. We find that CTLs show reduced migration on allogeneic islets in vivo compared to in vitro data, indicating CTL activation. Interestingly, the temporal infiltration pattern of T cells during rejection is precisely regulated, showing enrichment of CD4 T helper cells on the islets before arrival of CD8 CTLs. The adaptation of the ACE to immune responses enables the examination of the mechanism and regulation of CTL-mediated killing in vivo and to further investigate the killing in gene-deficient mice that resemble severe human immune diseases.

摘要

细胞毒性 T 淋巴细胞 (CTL) 通过杀死受感染和恶性细胞,成为我们免疫系统的重要组成部分。为了充分理解这个过程,有必要在生物体的生理环境中研究 CTL 功能,以解释它们与其他免疫细胞(如 CD4 T 辅助细胞和巨噬细胞)的相互作用。眼睛前房 (ACE) 最初是为糖尿病研究开发的,非常适合进行非侵入性和纵向体内成像。我们利用 ACE 窗口观察免疫反应,特别是 CTL 对胰岛细胞的同种异体排斥反应。我们通过重复双光子显微镜观察,从血管化后胰岛排斥反应的开始,一直持续到大约一个月的排斥反应结束。我们发现 CTL 在体内对同种异体胰岛的迁移能力明显低于体外数据,表明 CTL 被激活。有趣的是,排斥过程中 T 细胞的时间浸润模式受到精确调控,在 CD8 CTL 到达之前,CD4 T 辅助细胞在胰岛上富集。ACE 对免疫反应的适应使我们能够在体内检查 CTL 介导的杀伤的机制和调节,并进一步研究类似于严重人类免疫疾病的基因缺陷小鼠中的杀伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f6/7369940/d62f6f64b2e3/ijms-21-04660-g001.jpg

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