Miyake S, Sakurai T, Okumura K, Yagita H
Division of Rheumatology and Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Eur J Immunol. 1994 Sep;24(9):2000-5. doi: 10.1002/eji.1830240910.
In this study we investigated the receptors by which murine lymphocytes bind to collagen and laminin. To identify the collagen and laminin receptors, we generated three monoclonal antibodies, two of which (HM alpha 1 and HM alpha 2) could inhibit adhesion of activated T cells to collagen and laminin and one of which (HM alpha 6) could inhibit that to laminin. Biochemical studies showed that the antigens recognized by HM alpha 1, HM alpha 2, and HM alpha 6 are the mouse homologues of human VLA-1, VLA-2, and VLA-6, respectively. Finally, we demonstrated that both VLA-1 and VLA-2 contribute to the functional interaction between collagen and activated T cells, since HM alpha 1 and HM alpha 2 specifically inhibited collagen-induced TNF secretion from activated T cells. These results indicate that VLA-1 and VLA-2 play an important role in regulating adhesion and cytokine production of activated T cells.
在本研究中,我们调查了小鼠淋巴细胞与胶原蛋白和层粘连蛋白结合所通过的受体。为了鉴定胶原蛋白和层粘连蛋白受体,我们制备了三种单克隆抗体,其中两种(HMα1和HMα2)能够抑制活化T细胞与胶原蛋白和层粘连蛋白的黏附,另一种(HMα6)能够抑制活化T细胞与层粘连蛋白的黏附。生化研究表明,HMα1、HMα2和HMα6所识别的抗原分别是人类VLA-1、VLA-2和VLA-6的小鼠同源物。最后,我们证明VLA-1和VLA-2均参与了胶原蛋白与活化T细胞之间的功能相互作用,因为HMα1和HMα2特异性抑制了活化T细胞中胶原蛋白诱导的TNF分泌。这些结果表明,VLA-1和VLA-2在调节活化T细胞的黏附和细胞因子产生中起重要作用。