Department of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, Taiwan.
Cell Transplant. 2011;20(6):893-907. doi: 10.3727/096368910X550206. Epub 2010 Dec 22.
Embryonic stem (ES) cell transplantation represents a potential means for the treatment of degenerative diseases and injuries. As appropriate distribution of transplanted ES cells in the host tissue is critical for successful transplantation, the exploration of efficient strategies to enhance ES cell migration is warranted. In this study we investigated ES cell migration under the influence of various extracellular matrix (ECM) proteins, which have been shown to stimulate cell migration in various cell models with unclear effects on ES cells. Using two mouse ES (mES) cell lines, ESC 26GJ9012-8-2 and ES-D3 GL, to generate embryoid bodies (EBs), we examined the migration of differentiating cells from EBs that were delivered onto culture surfaces coated with or without collagen I, collagen IV, Matrigel, fibronectin, and laminin. Among these ECM proteins, collagen IV exhibited maximal migration enhancing effect. mES cells expressed α2 and β1 integrin subunits and the migration enhancing effect of collagen IV was prevented by RGD peptides as well as antibodies against α2 and β1 integrins, indicating that the enhancing effect of collagen IV on cell migration was mediated by α2β1 integrin. Furthermore, staining of actin cytoskeleton that links to integrins revealed well-developed stress fibers and long filopodia in mES cells cultured on collagen IV, and the actin-disrupting cytochalasin D abolished the collagen IV-enhanced cell migration. In addition, pretreatment of undifferentiated or differentiated mES cells with collagen IV resulted in improved engraftment and growth after transplantation into the subcutaneous tissue of nude mice. Finally, collagen IV pretreatment of osteogenically differentiated mES cells increased osteogenic differentiation-like tissue and decreased undifferentiation-like tissue in the grafts grown after transplantation. Our results demonstrated that collagen IV significantly enhanced the migration of differentiating ES cells through α2β1 integrin-mediated actin remodeling and could promote ES cell transplantation efficiency, which may be imperative to stem cell therapy.
胚胎干细胞 (ES) 移植代表了治疗退行性疾病和损伤的一种潜在方法。由于适当分布在宿主组织中的移植 ES 细胞对于成功移植至关重要,因此有必要探索增强 ES 细胞迁移的有效策略。在这项研究中,我们研究了各种细胞外基质 (ECM) 蛋白对 ES 细胞迁移的影响。这些 ECM 蛋白已被证明可刺激各种细胞模型中的细胞迁移,但对 ES 细胞的影响尚不清楚。我们使用两种小鼠 ES (mES) 细胞系 ESC 26GJ9012-8-2 和 ES-D3 GL 生成胚状体 (EB),检查了从 EB 分化而来的细胞在涂有或不涂胶原蛋白 I、胶原蛋白 IV、Matrigel、纤连蛋白和层粘连蛋白的培养表面上的迁移。在这些 ECM 蛋白中,胶原蛋白 IV 表现出最大的迁移增强作用。mES 细胞表达α2 和β1 整合素亚基,胶原蛋白 IV 的迁移增强作用可被 RGD 肽以及针对α2 和β1 整合素的抗体所阻止,表明胶原蛋白 IV 对细胞迁移的增强作用是由α2β1 整合素介导的。此外,与整合素相连的肌动蛋白细胞骨架染色显示,在胶原蛋白 IV 上培养的 mES 细胞中形成了发育良好的应力纤维和长丝状伪足,而破坏肌动蛋白的细胞松弛素 D 则消除了胶原蛋白 IV 增强的细胞迁移。此外,未经分化或分化的 mES 细胞用胶原蛋白 IV 预处理后,在移植到裸鼠皮下组织后,提高了植入物的植入和生长。最后,在用胶原蛋白 IV 预处理成骨分化的 mES 细胞后,增加了移植物中骨分化样组织的数量,并减少了未分化样组织的数量。我们的结果表明,胶原蛋白 IV 通过α2β1 整合素介导的肌动蛋白重塑显著增强了分化 ES 细胞的迁移,并能促进 ES 细胞移植效率,这对干细胞治疗可能至关重要。