Lu L S, Chen W F
Department of Immunology, Beijing Medical University.
Shi Yan Sheng Wu Xue Bao. 1994 Mar;27(1):71-7.
The biological significance of the signals triggered by the interaction of cell surface expressed LFA-1 and ICAM-1 has been investigated in Con A stimulated murine thymocytes. Addition of anti-LFA-1 or/and anti-ICAM-1 McAb to the thymocyte culture in the presence of Con A, the cell proliferation was profoundly inhibited. Such inhibitory effect was more significant by the addition of anti-LFA-1 than by the addition of anti-ICAM-1 McAb. FACS analysis revealed that the proliferation of CD8+ T cells was more sensitive to the inhibitory effect of anti-LFA-1 McAb than did the proliferation of CD4+ T cells. The anti-LFA-1 McAb imposed inhibitory effect, however, could be reversed by the supplementation of IL-2 in the initiation of the culture. The proliferation of cultured Con A activated T blast cells could no longer be inhibited by the addition of anti-LFA-1 McAb. Furthermore, neither anti-LFA-1 nor anti-ICAM-1 McAb could block PMA+A23187 induced thymocyte proliferation. The results imply that the ligand-receptor pair of LFA-1-ICAM-1 molecules also takes part in the early events of Con A activated signal transduction pathway which leads to the proliferation of thymocytes.
在伴刀豆球蛋白A(Con A)刺激的小鼠胸腺细胞中,已对细胞表面表达的淋巴细胞功能相关抗原-1(LFA-1)与细胞间黏附分子-1(ICAM-1)相互作用所触发信号的生物学意义进行了研究。在Con A存在的情况下,向胸腺细胞培养物中添加抗LFA-1或/和抗ICAM-1单克隆抗体(McAb),细胞增殖受到显著抑制。添加抗LFA-1比添加抗ICAM-1 McAb产生的这种抑制作用更显著。荧光激活细胞分选(FACS)分析显示,CD8 + T细胞的增殖比CD4 + T细胞的增殖对抗LFA-1 McAb的抑制作用更敏感。然而,抗LFA-1 McAb施加的抑制作用可通过在培养开始时补充白细胞介素-2(IL-2)来逆转。添加抗LFA-1 McAb不再能抑制培养的Con A激活的T母细胞的增殖。此外,抗LFA-1和抗ICAM-1 McAb均不能阻断佛波酯(PMA)+离子霉素(A23187)诱导的胸腺细胞增殖。结果表明,LFA-1-ICAM-1分子的配体-受体对也参与了导致胸腺细胞增殖的Con A激活信号转导途径的早期事件。