Hirao M, Sato N, Kondo T, Yonemura S, Monden M, Sasaki T, Takai Y, Tsukita S, Tsukita S
Department of Cell Biology, Faculty of Medicine, Kyoto University, Japan.
J Cell Biol. 1996 Oct;135(1):37-51. doi: 10.1083/jcb.135.1.37.
The ERM proteins, ezrin, radixin, and moesin, are involved in the actin filament/plasma membrane interaction as cross-linkers. CD44 has been identified as one of the major membrane binding partners for ERM proteins. To examine the CD44/ERM protein interaction in vitro, we produced mouse ezrin, radixin, moesin, and the glutathione-S-transferase (GST)/CD44 cytoplasmic domain fusion protein (GST-CD44cyt) by means of recombinant baculovirus infection, and constructed an in vitro assay for the binding between ERM proteins and the cytoplasmic domain of CD44. In this system, ERM proteins bound to GST-CD44cyt with high affinity (Kd of moesin was 9.3 +/- 1.6nM) at a low ionic strength, but with low affinity at a physiological ionic strength. However, in the presence of phosphoinositides (phosphatidylinositol [PI], phosphatidylinositol 4-monophosphate [4-PIP], and phosphatidylinositol 4.5-bisphosphate [4,5-PIP2]), ERM proteins bound with a relatively high affinity to GST-CD44cyt even at a physiological ionic strength: 4,5-PIP2 showed a marked effect (Kd of moesin in the presence of 4,5-PIP2 was 9.3 +/- 4.8 nM). Next, to examine the regulation mechanism of CD44/ERM interaction in vivo, we reexamined the immunoprecipitated CD44/ERM complex from BHK cells and found that it contains Rho-GDP dissociation inhibitor (GDI), a regulator of Rho GTPase. We then evaluated the involvement of Rho in the regulation of the CD44/ERM complex formation. When recombinant ERM proteins were added and incubated with lysates of cultured BHK cells followed by centrifugation, a portion of the recombinant ERM proteins was recovered in the insoluble fraction. This binding was enhanced by GTP gamma S and markedly suppressed by C3 toxin, a specific inhibitor of Rho, indicating that the GTP form of Rho in the lysate is required for this binding. A mAb specific for the cytoplasmic domain of CD44 also markedly suppressed this binding, identifying most of the binding partners for exogenous ERM proteins in the insoluble fraction as CD44. Consistent with this binding analysis, in living BHK cells treated with C3 toxin, most insoluble ERM proteins moved to soluble compartments in the cytoplasm, leaving CD44 free from ERM. These findings indicate that Rho regulates the CD44/ERM complex formation in vivo and that the phosphatidylinositol turnover may be involved in this regulation mechanism.
ERM 蛋白,即埃兹蛋白、根蛋白和膜突蛋白,作为交联剂参与肌动蛋白丝/质膜的相互作用。CD44 已被确定为 ERM 蛋白的主要膜结合伴侣之一。为了在体外检测 CD44/ERM 蛋白的相互作用,我们通过重组杆状病毒感染制备了小鼠埃兹蛋白、根蛋白、膜突蛋白以及谷胱甘肽 -S-转移酶(GST)/CD44 胞质结构域融合蛋白(GST-CD44cyt),并构建了一个用于检测 ERM 蛋白与 CD44 胞质结构域之间结合的体外试验。在这个系统中,ERM 蛋白在低离子强度下以高亲和力(膜突蛋白的解离常数 Kd 为 9.3±1.6nM)与 GST-CD44cyt 结合,但在生理离子强度下亲和力较低。然而,在磷脂酰肌醇(磷脂酰肌醇[PI]、磷脂酰肌醇 4-单磷酸[4-PIP]和磷脂酰肌醇 4,5-二磷酸[4,5-PIP2])存在的情况下,即使在生理离子强度下,ERM 蛋白也以相对较高的亲和力与 GST-CD44cyt 结合:4,5-PIP2 显示出显著作用(在 4,5-PIP2 存在下膜突蛋白的 Kd 为 9.3±4.8 nM)。接下来,为了检测体内 CD44/ERM 相互作用的调节机制,我们重新检测了从 BHK 细胞免疫沉淀得到的 CD44/ERM 复合物,发现它含有 Rho-GDP 解离抑制剂(GDI),一种 Rho GTP 酶的调节剂。然后我们评估了 Rho 在 CD44/ERM 复合物形成调节中的作用。当添加重组 ERM 蛋白并与培养的 BHK 细胞裂解物一起孵育然后离心时,一部分重组 ERM 蛋白在不溶性部分中被回收。这种结合被 GTPγS 增强,并被 Rho 的特异性抑制剂 C3 毒素显著抑制,表明裂解物中 Rho 的 GTP 形式是这种结合所必需的。一种针对 CD44 胞质结构域的单克隆抗体也显著抑制了这种结合,确定不溶性部分中外源 ERM 蛋白的大多数结合伴侣为 CD44。与这种结合分析一致,在用 C3 毒素处理的活 BHK 细胞中,大多数不溶性 ERM 蛋白转移到细胞质中的可溶性部分,使 CD44 与 ERM 分离。这些发现表明 Rho 在体内调节 CD44/ERM 复合物的形成,并且磷脂酰肌醇周转可能参与这种调节机制。