Tedder T F, Isaacs C M, Ernst T J, Demetri G D, Adler D A, Disteche C M
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, Massachusetts.
J Exp Med. 1989 Jul 1;170(1):123-33. doi: 10.1084/jem.170.1.123.
A cDNA encoding a new human lymphocyte cell surface molecule has been isolated and shown to identify a fourth member of a recently discovered family of adhesion proteins. This lymphocyte-associated molecule (LAM-1) is uniquely composed of multiple distinct domains, one domain homologous with animal lectins, one homologous with epidermal growth factor, and two short consensus repeat units similar to those found in C3/C4 binding proteins. This cDNA clone hybridized with RNAs found in B cell lines and T lymphocytes, but not with RNA from other cell types. The amino acid sequence of LAM-1 is 77% homologous with the sequence of the mouse lymphocyte homing receptor, suggesting that LAM-1 may function in human lymphocyte adhesion. The LAM-1 gene is located on chromosome 1q23-25, as is another member of this adhesion family, suggesting that this new family of proteins may be encoded by a cluster of "adhesion protein" loci.
一个编码新的人类淋巴细胞细胞表面分子的cDNA已被分离出来,并被证明可鉴定出最近发现的粘附蛋白家族的第四个成员。这种淋巴细胞相关分子(LAM-1)独特地由多个不同结构域组成,一个结构域与动物凝集素同源,一个与表皮生长因子同源,还有两个短共有重复单元,类似于在C3/C4结合蛋白中发现的那些。这个cDNA克隆与B细胞系和T淋巴细胞中的RNA杂交,但不与其他细胞类型的RNA杂交。LAM-1的氨基酸序列与小鼠淋巴细胞归巢受体的序列有77%的同源性,这表明LAM-1可能在人类淋巴细胞粘附中发挥作用。LAM-1基因位于1号染色体的1q23-25区域,这个粘附家族的另一个成员也是如此,这表明这个新的蛋白质家族可能由一组“粘附蛋白”基因座编码。