肿瘤坏死因子-α在转化CD4+ T细胞系中诱导的生长抑制和细胞死亡的作用

IF 2.9 4区 医学 Q3 IMMUNOLOGY Archivum Immunologiae et Therapiae Experimentalis Pub Date : 2023-02-01 DOI:10.1007/s00005-023-00670-3
Akshay G. Patel, Sarah Moxham, Anil K. Bamezai
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引用次数: 0

摘要

Ly-6A是一种细胞粘附和细胞信号蛋白,是Ly-6/uPAR超基因蛋白家族的成员。通过Ly-6A信号通路激活CD4+ T细胞系细胞内凋亡细胞死亡通路,如细胞色素C的释放和caspases 9和caspases 3的激活。此外,Ly-6A诱导细胞因子的产生和生长抑制。参与Ly-6A蛋白引发的不同细胞反应的机制仍然未知。为了检验这些不同反应的相关性,我们量化了促凋亡、生长抑制和肿瘤抑制细胞因子的产生,如TNF-α、TGF-β和相关蛋白GDF-10,以响应Ly-6A信号。抗ly - 6a单克隆抗体诱导的YH16.33 CD4+ T细胞株的激活产生低水平的TGF-β和GDF-10,但TNF-α水平升高。阻断TNF-α的生物活性可减少ly - 6a诱导的T细胞凋亡。在T细胞系中,ly - 6a诱导的反应是不同的,尽管在这些培养物中检测到高水平的TGF-β和GDF-10,但通过抗原受体复合物的信号传导不会引起生长抑制和凋亡。此外,在对抗原受体复合物信号的反应中,检测到较低量的TNF-α。这些结果表明TNF-α在观察到的Ly-6A诱导的生长抑制和凋亡中的作用,并为参与Ly-6A蛋白后在CD4+ T细胞中观察到的生物学上不同的反应提供了机制解释。此外,本文报道的研究结果将有助于理解由Ly-6A蛋白启动的抑制信号,特别是在其潜在的免疫检查点抑制T细胞作用的背景下。
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Ly-6A-Induced Growth Inhibition and Cell Death in a Transformed CD4+ T Cell Line: Role of Tumor Necrosis Factor-α

Ly-6A, a member of the Ly-6/uPAR supergene family of proteins, is a cell adhesion and cell signaling protein. Signaling through Ly-6A activates the cell-intrinsic apoptotic cell death pathway in CD4+ T cell lines, as indicated by the release of cytochrome C, and activation of caspases 9 and 3. In addition, Ly-6A induces cytokine production and growth inhibition. The mechanism underlying the distinct cellular responses that are triggered by engaging Ly-6A protein has remained unknown. To examine the relatedness of these distinct responses, we have quantified the production of pro-apoptotic, growth inhibitory and tumor suppressive cytokines, such as TNF-α, TGF-β and a related protein GDF-10, in response to Ly-6A signaling. Anti-Ly-6A monoclonal antibody-induced activation of YH16.33 CD4+ T cell line generated low levels of TGF-β and GDF-10 but elevated levels of TNF-α. Blocking the biological activity of TNF-α resulted in reduced Ly-6A-induced apoptosis in T cells. The Ly-6A-induced response in the T cell line was distinct, as signaling through the antigen receptor complex did not cause growth inhibition and apoptosis despite high levels of TGF-β and GDF-10 that were detected in these cultures. Additionally, in response to antigen receptor complex signaling, lower amount of TNF-α was detected. These results indicate the contribution of TNF-α in the observed Ly-6A-induced growth inhibition and apoptosis and provide a mechanistic explanation for the biologically distinct responses observed in CD4+ T cells after engaging Ly-6A protein. Additionally, the findings reported here will aid in the understanding of inhibitory signaling initiated by Ly-6A protein, especially in the context of its potential immune checkpoint inhibitory role in T cells.

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来源期刊
CiteScore
5.90
自引率
0.00%
发文量
26
审稿时长
>12 weeks
期刊介绍: Archivum Immunologiae et Therapiae Experimentalis (AITE), founded in 1953 by Ludwik Hirszfeld, is a bimonthly, multidisciplinary journal. It publishes reviews and full original papers dealing with immunology, experimental therapy, immunogenetics, transplantation, microbiology, immunochemistry and ethics in science.
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