Schriever F, Korinth D, Salahi A, Lefterova P, Schmidt-Wolf I G, Behr S I
Department of Hematology and Oncology, Virchow University Hospital, Humboldt Universität Berlin, Germany.
Eur J Immunol. 1997 Jan;27(1):35-9. doi: 10.1002/eji.1830270106.
Binding of T lymphocytes within the different compartments of the secondary lymphoid organs is crucial for the function of the cellular and the humoral immune response. It is still not known which adhesion molecules guide T cells to the distinct areas of the lymphoid microenvironment. In the current study an in situ adhesion assay was used to define the receptors for binding of T cells to human tonsils. The T cell lines Jurkat and MOLT-4 and normal, activated T cells were found to bind exclusively to germinal centers. Jurkat cells used the receptor pair integrin-alpha4 (VLA-4alpha)/VCAM-1, whereas activated MOLT-4 cells and normal T cells bound via both adhesion pathways, namely via integrin-alpha4/VCAM-1 and LFA-1/ICAM-1 and -2. It is suggested that these adhesion mechanisms are involved in the migration of T cells into the germinal centers of secondary lymphoid organs and that they influence the selection of B cells by apoptosis.
T淋巴细胞在二级淋巴器官不同区域的黏附对于细胞免疫应答和体液免疫应答的功能至关重要。目前仍不清楚是哪些黏附分子将T细胞引导至淋巴微环境的不同区域。在本研究中,采用原位黏附试验来确定T细胞与人扁桃体结合的受体。发现T细胞系Jurkat和MOLT-4以及正常活化的T细胞仅与生发中心结合。Jurkat细胞利用整合素α4(VLA-4α)/血管细胞黏附分子-1(VCAM-1)这一受体对,而活化的MOLT-4细胞和正常T细胞则通过两种黏附途径结合,即通过整合素α4/VCAM-1以及淋巴细胞功能相关抗原-1(LFA-1)/细胞间黏附分子-1(ICAM-1)和细胞间黏附分子-2(ICAM-2)。提示这些黏附机制参与T细胞迁移至二级淋巴器官的生发中心,并且它们通过凋亡影响B细胞的选择。