Jean Léolène, Yang Lijie, Majumdar Devi, Gao Yandong, Shi Mingjian, Brewer Bryson M, Li Deyu, Webb Donna J
a Department of Biological Sciences and Vanderbilt Kennedy Center for Research on Human Development ; Vanderbilt University ; Nashville , TN USA.
Cell Adh Migr. 2014;8(5):460-7. doi: 10.4161/19336918.2014.983778.
Cell migration is fundamental to a variety of physiological processes, including tissue development, homeostasis, and regeneration. Migration has been extensively studied with cells on 2-dimensional (2D) substrates, but much less is known about cell migration in 3D environments. Tissues and organs are 3D, which is the native environment of cells in vivo, pointing to a need to understand migration and the mechanisms that regulate it in 3D environments. To investigate cell migration in 3D environments, we developed microfluidic devices that afford a controlled, reproducible platform for generating 3D matrices. Using these devices, we show that the Rho family guanine nucleotide exchange factor (GEF) Asef2 inhibits cell migration in 3D type I collagen (collagen I) matrices. Treatment of cells with the myosin II (MyoII) inhibitor blebbistatin abolished the decrease in migration by Asef2. Moreover, Asef2 enhanced MyoII activity as shown by increased phosphorylation of serine 19 (S19). Furthermore, Asef2 increased activation of Rac, which is a Rho family small GTPase, in 3D collagen I matrices. Inhibition of Rac activity by treatment with the Rac-specific inhibitor NSC23766 abrogated the Asef2-promoted increase in S19 MyoII phosphorylation. Thus, our results indicate that Asef2 regulates cell migration in 3D collagen I matrices through a Rac-MyoII-dependent mechanism.
细胞迁移是多种生理过程的基础,包括组织发育、内稳态和再生。人们已在二维(2D)基质上对细胞迁移进行了广泛研究,但对于细胞在三维(3D)环境中的迁移了解较少。组织和器官是三维的,这是细胞在体内的天然环境,这表明有必要了解三维环境中的迁移及其调控机制。为了研究细胞在三维环境中的迁移,我们开发了微流控装置,该装置为生成三维基质提供了一个可控、可重复的平台。使用这些装置,我们发现Rho家族鸟嘌呤核苷酸交换因子(GEF)Asef2在三维I型胶原(胶原I)基质中抑制细胞迁移。用肌球蛋白II(MyoII)抑制剂blebbistatin处理细胞可消除Asef2导致的迁移减少。此外,如丝氨酸19(S19)磷酸化增加所示,Asef2增强了MyoII活性。此外,在三维胶原I基质中,Asef2增加了Rac的激活,Rac是一种Rho家族小GTP酶。用Rac特异性抑制剂NSC23766处理抑制Rac活性,可消除Asef2促进的S19 MyoII磷酸化增加。因此,我们的结果表明,Asef2通过Rac-MyoII依赖性机制调节三维胶原I基质中的细胞迁移。