Mercurio A M, Rabinovitz I, Shaw L M
Division of Cancer Biology and Angiogenesis, Department of Pathology, Beth Israel Deaconess Medical Center, and Harvard Medical School, Boston, Massachusetts 02115, USA.
Curr Opin Cell Biol. 2001 Oct;13(5):541-5. doi: 10.1016/s0955-0674(00)00249-0.
Although the involvement of alpha 6 beta 4, an integrin laminin receptor, in hemidesmosome organization has dominated the study of this integrin, recent studies are revealing novel functions for alpha 6 beta 4 in the migration of epithelial and carcinoma cells. The engagement of laminin by alpha 6 beta 4 can stabilize actin-rich protrusions and mediate traction forces necessary for cell movement. This integrin also has a significant impact on signaling molecules that stimulate migration and invasion, especially PI3-K and Rho GTPases. Activation of PI3-K by alpha 6 beta 4 enhances the formation of actin protrusions, and it may stimulate the function of other integrins, such as alpha 3 beta 1, that are also important for epithelial migration. Signaling through alpha 6 beta 4 may not always depend on the adhesive functions of this integrin, a possibility that has profound implications for migration and invasion because it implies that the ability of alpha 6 beta 4 to stimulate these processes is not limited to specific matrix environments.
尽管整联蛋白层粘连蛋白受体α6β4参与半桥粒组织的研究主导了对该整联蛋白的研究,但最近的研究揭示了α6β4在上皮细胞和癌细胞迁移中的新功能。α6β4与层粘连蛋白的结合可以稳定富含肌动蛋白的突起,并介导细胞运动所需的牵引力。这种整联蛋白对刺激迁移和侵袭的信号分子也有显著影响,尤其是PI3-K和Rho GTPases。α6β4激活PI3-K可增强肌动蛋白突起的形成,并且可能刺激其他对上皮迁移也很重要的整联蛋白,如α3β1的功能。通过α6β4的信号传导可能并不总是依赖于该整联蛋白的粘附功能,这种可能性对迁移和侵袭具有深远影响,因为这意味着α6β4刺激这些过程的能力不限于特定的基质环境。