Siu C H, Wong L M, Lam T Y, Kamboj R K, Choi A, Cho A
Banting and Best Department of Medical Research, Charles H. Best Institute, University of Toronto, Ont., Canada.
Biochem Cell Biol. 1988 Oct;66(10):1089-99. doi: 10.1139/o88-126.
During development of the cellular slime mold Dictyostelium discoideum, cells migrate in response to cAMP to form aggregates, which give rise to fruiting bodies consisting of two major cell types: spores and stalk cells. Multicellularity is achieved by the expression of two types of cell-cell adhesion sites. The EDTA-sensitive binding sites are expressed at the initial stage of development. At the aggregation stage, cells acquire EDTA-resistant binding sites, which are mediated by a cell-surface glycoprotein of Mr80,000 (gp80). gp80 is preferentially associated with cell surface filopodia, which are probably involved in the initiation of contact formation between cells. Covaspheres conjugated with gp80 bind specifically to aggregation-stage cells. The binding can be inhibited by precoating cells with an anti-gp80 monoclonal antibody, thus suggesting that gp80 mediates cell-cell binding via homophilic interaction. The structure of gp80 predicted from its cDNA sequence can be divided into three major domains: a membrane anchor, a hinge, and a globular region. An analysis of fusion proteins containing different gp80 segments shows that the cell-binding activity resides in the globular region. In the postaggregation stages, gp80 is replaced by other surface glycoproteins in maintaining cell-cell adhesion. One of them has a Mr of 150,000 (gp150). Anti-gp150 antibodies have no effect on aggregation-stage cells, but they disrupt cell-cell adhesion at subsequent stages. It becomes evident that the complex phenomena of cell adhesion and tissue organization involve the participation of a number of surface glycoproteins.
在细胞黏菌盘基网柄菌的发育过程中,细胞会响应环磷酸腺苷(cAMP)进行迁移以形成聚集体,这些聚集体进而产生由两种主要细胞类型组成的子实体:孢子和柄细胞。多细胞性是通过两种类型的细胞间黏附位点的表达来实现的。对乙二胺四乙酸(EDTA)敏感的结合位点在发育初期表达。在聚集阶段,细胞获得对EDTA有抗性的结合位点,这些位点由分子量为80,000的细胞表面糖蛋白(gp80)介导。gp80优先与细胞表面丝状伪足相关联,丝状伪足可能参与细胞间接触形成的起始过程。与gp80偶联的共球体能特异性结合聚集阶段的细胞。这种结合可以通过用抗gp80单克隆抗体预先包被细胞来抑制,这表明gp80通过同型相互作用介导细胞间结合。根据其cDNA序列预测的gp80结构可分为三个主要结构域:一个膜锚、一个铰链区和一个球状区域。对包含不同gp80片段的融合蛋白的分析表明,细胞结合活性存在于球状区域。在聚集后阶段,gp80被其他表面糖蛋白取代以维持细胞间黏附。其中一种糖蛋白的分子量为150,000(gp150)。抗gp150抗体对聚集阶段的细胞没有影响,但它们会破坏后续阶段的细胞间黏附。很明显,细胞黏附和组织组织的复杂现象涉及多种表面糖蛋白的参与。