Genetics Division, National Cancer Center Research Institute, Tokyo 104-0045, Japan; Tumor Suppression and Functional Genomics Project, National Cancer Center Research Institute, Tokyo 104-0045, Japan.
Tumor Suppression and Functional Genomics Project, National Cancer Center Research Institute, Tokyo 104-0045, Japan; Division of Molecular Pathology, Department of Cancer Biology, Institute of Medical Science, University of Tokyo, Tokyo 108-8639, Japan.
J Biol Chem. 2010 May 14;285(20):15511-15522. doi: 10.1074/jbc.M109.076653. Epub 2010 Mar 9.
CADM1 encodes a multifunctional immunoglobulin-like cell adhesion molecule whose cytoplasmic domain contains a type II PSD95/Dlg/ZO-1 (PDZ)-binding motif (BM) for associating with other intracellular proteins. Although CADM1 lacks expression in T lymphocytes of healthy individuals, it is overexpressed in adult T-cell leukemia-lymphoma (ATL) cells. It has been suggested that the expression of CADM1 protein promotes infiltration of leukemic cells into various organs and tissues, which is one of the frequent clinical manifestations of ATL. Amino acid sequence alignment revealed that Tiam1 (T-lymphoma invasion and metastasis 1), a Rac-specific guanine nucleotide exchange factor, has a type II PDZ domain similar to those of membrane-associated guanylate kinase homologs (MAGUKs) that are known to bind to the PDZ-BM of CADM1. In this study, we demonstrated that the cytoplasmic domain of CADM1 directly interacted with the PDZ domain of Tiam1 and induced formation of lamellipodia through Rac activation in HTLV-I-transformed cell lines as well as ATL cell lines. Our results indicate that Tiam1 integrates signals from CADM1 to regulate the actin cytoskeleton through Rac activation, which may lead to tissue infiltration of leukemic cells in ATL patients.
CADM1 编码一种多功能免疫球蛋白样细胞黏附分子,其细胞质结构域包含一个 PSD95/Dlg/ZO-1(PDZ)结合基序(BM),用于与其他细胞内蛋白结合。虽然 CADM1 在健康个体的 T 淋巴细胞中不表达,但在成人 T 细胞白血病/淋巴瘤(ATL)细胞中过度表达。有人提出,CADM1 蛋白的表达促进了白血病细胞浸润到各种器官和组织中,这是 ATL 的常见临床表现之一。氨基酸序列比对表明,Tiam1(T 淋巴细胞侵袭和转移 1)是 Rac 特异性鸟嘌呤核苷酸交换因子,具有与已知与 CADM1 的 PDZ-BM 结合的膜相关鸟苷酸激酶同源物(MAGUKs)的类似的 II 型 PDZ 结构域。在这项研究中,我们证明 CADM1 的细胞质结构域直接与 Tiam1 的 PDZ 结构域相互作用,并通过 Rac 激活诱导形成片状伪足,这在 HTLV-I 转化的细胞系以及 ATL 细胞系中均有体现。我们的结果表明,Tiam1 通过 Rac 激活整合来自 CADM1 的信号,从而调节肌动蛋白细胞骨架,这可能导致 ATL 患者白血病细胞浸润组织。