Mosabbir Abdullah A, Truong Kevin
Institute of Biomaterials and Biomedical Engineering, University of Toronto , 164 College Street, Toronto, Ontario M5S 3G9, Canada.
Edward S. Rogers Sr. Department of Electrical and Computer Engineering, University of Toronto , 10 King's College Circle, Toronto, Ontario M5S 3G4, Canada.
ACS Synth Biol. 2018 Feb 16;7(2):718-726. doi: 10.1021/acssynbio.7b00415. Epub 2018 Jan 26.
Magnetoreception can be generally defined as the ability to transduce the effects of a magnetic field into a cellular response. Magnetic stimulation at the cellular level is particularly attractive due to its ability for deep penetration and minimal invasiveness, allowing remote regulation of engineered biological processes. Previously, a magnetic-responsive genetic circuit was engineered using the transient receptor potential vanilloid 1 (TRPV1) and the iron containing ferritin protein (i.e., the TF circuit). In this study, we combined the TF circuit with a Ca activated RhoA protein (CaRQ) to allow a magnetic field to remotely regulate cell migration. Cells expressing the TF circuit and CaRQ exhibited consistent dynamic protrusions, leading to migration along a porous membrane, directed spreading in response to a magnetic field gradient, as well as wound healing. This work offers a compelling interface for programmable electrical devices to control the migration of living systems for potential applications in cell-based therapy.
磁感受一般可定义为将磁场效应转化为细胞反应的能力。细胞水平的磁刺激因其具有深度穿透能力和最小侵入性,能够远程调节工程生物过程,故而特别具有吸引力。此前,利用瞬时受体电位香草酸受体1(TRPV1)和含铁铁蛋白(即TF电路)构建了一个磁响应基因电路。在本研究中,我们将TF电路与钙激活的RhoA蛋白(CaRQ)相结合,使磁场能够远程调节细胞迁移。表达TF电路和CaRQ的细胞表现出一致的动态突起,导致细胞沿着多孔膜迁移,响应磁场梯度定向扩散,以及伤口愈合。这项工作为可编程电子设备提供了一个引人注目的接口,以控制生物系统的迁移,在基于细胞的治疗中具有潜在应用价值。