Sewell W A, Brown M H, Owen M J, Fink P J, Kozak C A, Crumpton M J
Eur J Immunol. 1987 Jul;17(7):1015-20. doi: 10.1002/eji.1830170718.
The human T lymphocyte antigen CD2 (T11, sheep erythrocyte receptor) is expressed on all peripheral T cells and all but the most immature thymocytes. Experiments with monoclonal antibodies against CD2 suggest that CD2 is the cell surface receptor for a natural ligand involved in T cell proliferation. Clarification of the functional role of CD2 would be facilitated by the identification of CD2 in the mouse. However, antibodies that recognize the murine homologue have not been described. An alternative approach to the identification of the murine homologue was to use cross-species DNA hybridization, employing human CD2 cDNA as a probe. Clones encoding the murine homologue were isolated from a murine T helper cell cDNA library. The murine cDNA sequence encoded a predicted mature polypeptide of 322 amino acids that showed 54% identity with the predicted human sequence. As with the human polypeptide, the cytoplasmic domain was large, and rich in proline and basic residues. CD2 mRNA was expressed in murine thymus and spleen, and in the T cell line EL4. The murine CD2 gene was assigned to chromosome 3 by Southern blot analysis of mouse-hamster somatic cell hybrids. A rabbit antiserum raised against purified human CD2, precipitated from surface-labeled mouse thymocytes a glycoprotein of Mr 55,000-66,000 which decreased to Mr 35,000 on digestion with endo-beta-acetylglucosaminidase F. These sizes are consistent with those predicted for the murine CD2 antigen from the cDNA sequence.
人类T淋巴细胞抗原CD2(T11,绵羊红细胞受体)在所有外周T细胞以及除最不成熟的胸腺细胞外的所有胸腺细胞上均有表达。针对CD2的单克隆抗体实验表明,CD2是参与T细胞增殖的天然配体的细胞表面受体。在小鼠中鉴定CD2将有助于阐明其功能作用。然而,尚未描述识别鼠类同源物的抗体。鉴定鼠类同源物的另一种方法是使用跨物种DNA杂交,用人CD2 cDNA作为探针。从鼠类T辅助细胞cDNA文库中分离出编码鼠类同源物的克隆。鼠类cDNA序列编码一个预测的322个氨基酸的成熟多肽,与预测的人类序列具有54%的同一性。与人类多肽一样,胞质结构域较大,富含脯氨酸和碱性残基。CD2 mRNA在鼠类胸腺和脾脏以及T细胞系EL4中表达。通过对小鼠-仓鼠体细胞杂种的Southern印迹分析,将鼠类CD2基因定位到3号染色体。用针对纯化的人类CD2产生的兔抗血清,从表面标记的小鼠胸腺细胞中沉淀出一种分子量为55,000 - 66,000的糖蛋白,用内切β-乙酰葡糖胺酶F消化后降至35,000。这些大小与从cDNA序列预测的鼠类CD2抗原的大小一致。