Hayes Sandra M, Love Paul E
Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Immunity. 2002 Jun;16(6):827-38. doi: 10.1016/s1074-7613(02)00320-5.
Alpha beta and gamma delta T cells are distinguished by the clonotypic subunits contained within their TCRs. Although the alpha beta TCR has been well characterized, much less is known about the gamma delta TCR. Here, we report that, unlike alpha beta T CRs, most gamma delta TCRs expressed on ex vivo gamma delta T cells lack CD3 delta. Despite this structural difference, signal transduction by the gamma delta TCR is superior to that of the alpha beta TCR, as measured by its ability to induce calcium mobilization, ERK activation, and cellular proliferation. Additionally, the TCR complexes expressed on primary gamma delta T cells contain only zeta zeta homodimers; however, following activation and expansion, Fc epsilon R1 gamma is expressed and is included in the gamma delta TCR complex. These results reveal fundamental differences in the primary structure and signaling potential of the alpha beta- and gamma delta TCR complexes.
αβ和γδ T细胞通过其TCR中包含的克隆型亚基来区分。尽管αβ TCR已得到充分表征,但对γδ TCR的了解却少得多。在此,我们报告,与αβ TCR不同,体外γδ T细胞上表达的大多数γδ TCR缺乏CD3δ。尽管存在这种结构差异,但通过其诱导钙动员、ERK激活和细胞增殖的能力来衡量,γδ TCR的信号转导优于αβ TCR。此外,原代γδ T细胞上表达的TCR复合物仅包含ζζ同型二聚体;然而,在激活和扩增后,FcεR1γ表达并被纳入γδ TCR复合物中。这些结果揭示了αβ和γδ TCR复合物在一级结构和信号转导潜力方面的根本差异。