Po J L, Mazer B, Jensen G S
Royal Victoria Hospital, Department of Surgery, Montreal, Quebec, Canada.
Biochem Biophys Res Commun. 1995 Dec 26;217(3):1145-50. doi: 10.1006/bbrc.1995.2888.
We report the induction of intracellular calcium mobilization [Ca2+]i in normal peripheral blood mononuclear cells (PBMC) and Daudi cells following binding with the L-selectin monoclonal antibody FMC46. The [Ca2+]i signal was mediated directly by binding of FMC46 without cross-linking antibodies. Increased [Ca2+]i was not induced by other L-selectin antibodies tested (TQ1, Leu8, Lam1.3). The increase in [Ca2+]i was rapid and was blocked completely by BAPTA, an agent which chelates intracellular calcium. The increase in [Ca2+]i was observed in calcium-containing as well as calcium free medium, suggesting that FMC46 caused release of Ca2+ from intracellular stores. In both PBMC and Daudi cells, previous signaling via L-selectin still allowed signaling through cross-linking of surface antigen receptor. These data provide evidence for direct alteration of the state of lymphocytes after ligation of a specific L-selectin epitope. L-selectin-mediated signaling does not desensitize signaling through the antigen-receptor and could therefore play a role in preactivating lymphocytes during endothelial transmigration into lymphoid tissues.
我们报告了与L-选择素单克隆抗体FMC46结合后,正常外周血单个核细胞(PBMC)和Daudi细胞内钙离子动员[Ca2+]i的诱导情况。[Ca2+]i信号是由FMC46的直接结合介导的,无需交联抗体。所测试的其他L-选择素抗体(TQ1、Leu8、Lam1.3)未诱导[Ca2+]i增加。[Ca2+]i的增加迅速,且被螯合细胞内钙的试剂BAPTA完全阻断。在含钙和无钙培养基中均观察到[Ca2+]i增加,这表明FMC46导致Ca2+从细胞内储存库释放。在PBMC和Daudi细胞中,先前通过L-选择素的信号传导仍允许通过表面抗原受体交联进行信号传导。这些数据为特定L-选择素表位连接后淋巴细胞状态的直接改变提供了证据。L-选择素介导的信号传导不会使通过抗原受体的信号传导脱敏,因此可能在内皮细胞迁移到淋巴组织过程中预激活淋巴细胞方面发挥作用。