Twal W O, Czirok A, Hegedus B, Knaak C, Chintalapudi M R, Okagawa H, Sugi Y, Argraves W S
Medical University of South Carolina, Department of Cell Biology, 171 Ashley Avenue, Charleston, SC 29425-2204, USA.
J Cell Sci. 2001 Dec;114(Pt 24):4587-98. doi: 10.1242/jcs.114.24.4587.
Fibulin-1 is an extracellular matrix protein often associated with fibronectin (FN) in vivo. In this study, the ability of fibulin-1 to modulate adhesion, spreading and motility-promoting activities of FN was investigated. Fibulin-1 was found to have pronounced inhibitory effects on the cell attachment and spreading promoted by FN. Fibulin-1 was also found to inhibit the motility of a variety of cell types on FN substrata. For example, the FN-dependent haptotactic motility of breast carcinoma (MDA MB231) cells, epidermal carcinoma (A431), melanoma (A375 SM), rat pulmonary aortic smooth muscle cells (PAC1) and Chinese hamster ovary (CHO) cells was inhibited by the presence of fibulin-1 bound to FN-coated Boyden chamber membranes. Cells transfected to overproduce fibulin-1 displayed reduced velocity, distance of movement and persistence time on FN substrata. Similarly, the incorporation of fibulin-1 into FN-containing type I collagen gels inhibited the invasion of endocardial cushion mesenchymal cells migrating from cultured embryonic heart explants. By contrast, incorporation of fibulin-1 into collagen gels lacking FN had no effect on the migration of endocardial cushion cells. These results suggest that the motility-suppressive effects of fibulin-1 might be FN specific. Furthermore, such effects are cell-type specific, in that the migration of gingival fibroblasts and endothelial cells on FN substrata is not responsive to fibulin-1. Additional studies found that the mechanism for the motility-suppressive effects of fibulin-1 does not involve perturbations of interactions between alpha5beta1 or alpha4 integrins, or heparan sulfate proteoglycans with FN. However, fibulin-1 was found to inhibit extracellular signal regulated kinase (ERK) activation and to suppress phosphorylation of myosin heavy chain. This ability to influence signal transduction cascades that modulate the actin-myosin motor complex might be the basis for the effects of fibulin-1 on adhesion and motility.
纤维连接蛋白-1是一种细胞外基质蛋白,在体内常与纤连蛋白(FN)相关联。在本研究中,对纤维连接蛋白-1调节FN的黏附、铺展和促进运动活性的能力进行了研究。发现纤维连接蛋白-1对FN促进的细胞附着和铺展具有显著的抑制作用。还发现纤维连接蛋白-1抑制多种细胞类型在FN基质上的运动。例如,与包被有FN的博伊登小室膜结合的纤维连接蛋白-1抑制了乳腺癌(MDA MB231)细胞、表皮癌(A431)细胞、黑色素瘤(A375 SM)细胞、大鼠肺动脉平滑肌细胞(PAC1)和中国仓鼠卵巢(CHO)细胞的FN依赖性趋触性运动。转染以过量表达纤维连接蛋白-1的细胞在FN基质上的速度、移动距离和持续时间降低。同样,将纤维连接蛋白-1掺入含FN的I型胶原凝胶中可抑制从培养的胚胎心脏外植体迁移的心内膜垫间充质细胞的侵袭。相比之下,将纤维连接蛋白-1掺入缺乏FN的胶原凝胶中对心内膜垫细胞的迁移没有影响。这些结果表明,纤维连接蛋白-1的运动抑制作用可能是FN特异性的。此外,这种作用具有细胞类型特异性,因为牙龈成纤维细胞和内皮细胞在FN基质上的迁移对纤维连接蛋白-1不敏感。进一步的研究发现,纤维连接蛋白-1运动抑制作用的机制不涉及α5β1或α4整合素或硫酸乙酰肝素蛋白聚糖与FN之间相互作用的扰动。然而,发现纤维连接蛋白-1抑制细胞外信号调节激酶(ERK)的激活并抑制肌球蛋白重链的磷酸化。这种影响调节肌动蛋白-肌球蛋白运动复合体的信号转导级联反应的能力可能是纤维连接蛋白-1对黏附和运动产生影响的基础。