Irie H Y, Mong M S, Itano A, Crooks M E, Littman D R, Burakoff S J, Robey E
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 1998 Jul 1;161(1):183-91.
Previous studies have shown that CD8 beta plays a role in both enhancing CD8 alpha-associated Lck kinase activity and promoting the development of CD8-lineage T cells. To examine the role of this enhancement in the maturation of CD8-lineage cells, we assessed CD8 alpha-associated Lck kinase activity in both T cell hybridomas and thymocytes of mice expressing CD8 beta mutations known to impair CD8 T cell development. Lack of CD8 beta expression or expression of a cytoplasmic domain-deleted CD8 beta resulted in a severalfold reduction in CD8 alpha-associated Lck kinase activity compared with that observed with cells expressing wild-type CD8 beta chain. This analysis indicated a critical role for the cytoplasmic domain of CD8 beta in the regulation of CD8 alpha-associated Lck activity. Decreased CD8 alpha-associated Lck activity observed with the various CD8 beta mutations also correlated with diminished in vivo cellular tyrosine phosphorylation. In addition, analysis of CD8 beta mutant mice (CD8 beta-/- or cytoplasmic domain-deleted CD8 beta transgenic) indicated that the degree of reduction in CD8 alpha-associated Lck activity associated with each mutation correlated with the severity of developmental impairment. These results support the importance of CD8 beta-mediated enhancement of CD8 alpha-associated Lck kinase activity in the differentiation of CD8 single-positive thymocytes.
先前的研究表明,CD8β在增强与CD8α相关的Lck激酶活性以及促进CD8谱系T细胞的发育中均发挥作用。为了研究这种增强作用在CD8谱系细胞成熟过程中的作用,我们在表达已知会损害CD8 T细胞发育的CD8β突变的小鼠的T细胞杂交瘤和胸腺细胞中评估了与CD8α相关的Lck激酶活性。与表达野生型CD8β链的细胞相比,缺乏CD8β表达或表达缺失胞质结构域的CD8β会导致与CD8α相关的Lck激酶活性降低数倍。该分析表明CD8β的胞质结构域在调节与CD8α相关的Lck活性中起关键作用。在各种CD8β突变中观察到的与CD8α相关的Lck活性降低也与体内细胞酪氨酸磷酸化减少相关。此外,对CD8β突变小鼠(CD8β-/-或缺失胞质结构域的CD8β转基因小鼠)的分析表明,与每个突变相关的与CD8α相关的Lck活性降低程度与发育障碍的严重程度相关。这些结果支持了CD8β介导的增强与CD8α相关的Lck激酶活性在CD8单阳性胸腺细胞分化中的重要性。