Laboratoire Adhesion et Inflammation, UMR INSERM 1067, UMR CNRS 7333, Aix-Marseille Université, Case 937, CEDEX 09, 13288 Marseille, France.
Assistance Publique-Hôpitaux de Marseille, Lab. Immunologie, Hôpital de la Concception, 13005 Marseille, France.
Cells. 2021 Feb 18;10(2):429. doi: 10.3390/cells10020429.
The scanning of surrounding tissues by T lymphocytes to detect cognate antigens requires high speed, sensitivity and specificity. T-cell receptor (TCR) co-receptors such as CD8 increase detection performance, but the exact mechanism remains incompletely understood. Here, we used a laminar flow chamber to measure at the single molecule level the kinetics of bond formation and rupture between TCR- transfected CD8+ and CD8- Jurkat cells and surfaces coated with five peptide-exposing major histocompatibility antigens (pMHCs) of varying activating power. We also used interference reflection microscopy to image the spreading of these cells dropped on pMHC-exposing surfaces. CD8 did not influence the TCR-pMHC interaction during the first few seconds following cell surface encounter, but it promoted the subsequent spreading responses, suggesting that CD8 was involved in early activation rather than binding. Further, the rate and extent of spreading, but not the lag between contact and spreading initiation, depended on the pMHC. Elucidating T-lymphocyte detection strategy may help unravel underlying signaling networks.
T 细胞通过扫描周围组织来检测同源抗原,这需要高速、高灵敏度和高特异性。T 细胞受体 (TCR) 共受体,如 CD8,可提高检测性能,但确切的机制仍不完全清楚。在这里,我们使用层流室在单细胞水平上测量 TCR 转染的 CD8+和 CD8- Jurkat 细胞与涂有不同激活能力的五种肽暴露主要组织相容性抗原 (pMHC) 的表面之间键的形成和断裂的动力学。我们还使用干涉反射显微镜来成像这些细胞在 pMHC 暴露表面上的扩展。在细胞表面相遇后的最初几秒钟内,CD8 并没有影响 TCR-pMHC 相互作用,但它促进了随后的扩展反应,这表明 CD8 参与了早期激活而不是结合。此外,扩展的速率和程度,但不是接触和扩展开始之间的滞后时间,取决于 pMHC。阐明 T 淋巴细胞的检测策略可能有助于揭示潜在的信号转导网络。