Reinis M, Morra M, Funaro A, Di Primio R, Malavasi F
Laboratory of Cell Biology, University of Torino Medical School, Italy.
J Biol Regul Homeost Agents. 1997 Oct-Dec;11(4):137-42.
CD38 is a multifunctional membrane surface glycoprotein expressed by different cells and tissues, including T cells at certain stages of their development. Besides its involvement in transmembrane signaling, CD38 play a role in cell adhesion processes. Structurally, membrane CD38 was reported as presenting lateral associations with molecules involved in recognition and signaling, namely with the TCR/CD3 complex in T cells. Here we report that ligation of CD38 by agonistic and non-agonistic monoclonal antibodies exerts different effects on T cells, the former inducing down-modulation of the associated molecules, probably through a protein kinase C-dependent mechanism. This observation supports the view that the reduced expression of TCR/CD3 is secondary to interplay with CD38-mediated signaling, which partially overlaps with the CD3-mediated pathway. CD3 ligation by monoclonal antibodies leads not only to the expected internalization of the TCR/CD3 complex but also to down-modulation of surface CD38. The results obtained indicate that CD38 is closely associated with the CD3/TCR complex and that co-modulation of CD38 with TCR/CD3 is a critical step in signaling processes on T lymphocytes.
CD38是一种多功能膜表面糖蛋白,由不同的细胞和组织表达,包括处于其发育特定阶段的T细胞。除了参与跨膜信号传导外,CD38还在细胞粘附过程中发挥作用。在结构上,据报道膜CD38与参与识别和信号传导的分子存在侧向关联,即在T细胞中与TCR/CD3复合物存在侧向关联。在此我们报告,激动性和非激动性单克隆抗体对CD38的连接对T细胞产生不同影响,前者可能通过蛋白激酶C依赖性机制诱导相关分子的下调。这一观察结果支持了以下观点,即TCR/CD3表达的降低是与CD38介导的信号相互作用的结果,该信号与CD3介导的途径部分重叠。单克隆抗体对CD3的连接不仅导致TCR/CD3复合物预期的内化,还导致表面CD38的下调。所得结果表明,CD38与CD3/TCR复合物密切相关,并且CD38与TCR/CD3的共同调节是T淋巴细胞信号传导过程中的关键步骤。