Pickl W F, Majdic O, Fischer G F, Petzelbauer P, Faé I, Waclavicek M, Stöckl J, Scheinecker C, Vidicki T, Aschauer H, Johnson J P, Knapp W
Institute of Immunology, University of Vienna, Austria.
J Immunol. 1997 Mar 1;158(5):2107-15.
Extravasation and tissue infiltration of leukocytes and metastatic tumor cells require the regulated expression and function of adhesive and pro-proteolytic surface molecules. We demonstrate here that human T cells, upon activation, neo-express the melanoma metastasis-associated surface molecule MUC18/melanoma cell adhesion molecule (MCAM). Expression of MUC18/MCAM (CD146) on T cells could be identified with two mAbs (541-10B2 and 541-2E5) obtained after immunization with HUT102 T cells and found to react with activated T cells. The specificity of our mAbs for MUC18/MCAM (CD146) was revealed by 1) definition of the appropriate molecular mass of approximately 110 kDa unreduced and 120 kDa reduced, 2) reactivity of mAbs with MUC18/MCAM (CD146) cDNA-transfected mouse L cells, 3) conclusive crosswise immunoblotting experiments with MUC18/MCAM (CD146)-specific mAbs, and 4) N-terminal amino acid sequencing of precipitated protein. In vitro activation by PHA caused neo-expression of MUC18/MCAM (CD146) on peripheral blood T cells within 1 day of stimulation, reaching a maximum on day 3. In vivo expression of MUC18/MCAM (CD146) was confirmed on CD3+ T cells infiltrating delayed-type hypersensitivity lesions of the skin, on synovial fluid T cells of rheumatoid arthritis patients, and on distinct T leukemia cells. MUC18/MCAM (CD146) cell surface expression on activated T cells is mirrored by the presence of specific mRNA. Leukocytes of healthy donors do not show significant MUC18/MCAM (CD146) expression. The finding that MUC18/MCAM (CD146) is also expressed on activated T cells might suggest that this adhesion molecule is involved in the extravasation and/or homing of activated T cells.
白细胞和转移性肿瘤细胞的外渗及组织浸润需要黏附性和促蛋白水解表面分子的调控表达及功能。我们在此证明,人T细胞激活后会新表达黑色素瘤转移相关表面分子MUC18/黑色素瘤细胞黏附分子(MCAM)。用HUT102 T细胞免疫后获得的两种单克隆抗体(541 - 10B2和541 - 2E5)可识别T细胞上MUC18/MCAM(CD146)的表达,且发现其与活化T细胞发生反应。我们的单克隆抗体对MUC18/MCAM(CD146)的特异性通过以下方式得以揭示:1)确定未还原时约110 kDa、还原时约120 kDa的合适分子量;2)单克隆抗体与MUC18/MCAM(CD146)cDNA转染的小鼠L细胞的反应性;3)用MUC18/MCAM(CD146)特异性单克隆抗体进行的决定性交叉免疫印迹实验;4)沉淀蛋白的N端氨基酸测序。PHA体外激活导致外周血T细胞在刺激后1天内新表达MUC18/MCAM(CD146),在第3天达到最大值。在浸润皮肤迟发型超敏反应病变的CD3⁺T细胞、类风湿关节炎患者的滑液T细胞以及不同的T白血病细胞上证实了MUC18/MCAM(CD146)的体内表达。活化T细胞上MUC18/MCAM(CD146)的细胞表面表达与特异性mRNA的存在相对应。健康供体的白细胞未显示出明显的MUC18/MCAM(CD146)表达。MUC18/MCAM(CD146)也在活化T细胞上表达这一发现可能表明该黏附分子参与了活化T细胞的外渗和/或归巢。