Mitra Bhaskar, Jindal Rohit, Lee Serom, Xu Dong Dave, Li Lulu, Sharma Nripen, Maguire Tim, Schloss Rene, Yarmush Martin L
Department of Biomedical Engineering, Rutgers University, 599 Taylor Road, 08854, Piscataway, NJ.
Center for Engineering in Medicine and the Department of Surgery, Massachusetts General Hospital, and the Shriners Burns Hospital, Boston, MA, 02114.
RSC Adv. 2013 Sep 28;3(36):16002-16010. doi: 10.1039/C3RA41308J. Epub 2013 Jul 5.
Dendritic cells are the principal antigen presenting cells that are responsible for acquiring and transporting antigen from the peripheral tissue to the secondary lymphoid tissue. There they present it to T cells which ultimately initiate an antigen specific immune response. , the migration of dendritic cells (DCs) and T cell activation are intimately linked. However, systems that facilitate integrated evaluation of DC chemotaxis and resulting T cell activation by migrated DCs are lacking. In this work, we have developed a microfabricated platform that integrates DC chemotaxis with T cell activation. The basic design of the microdevice includes two layers of PDMS, with the top layer comprising the chemotaxis compartment and the bottom layer containing a T cell compartment. In the chemotaxis compartment, the DCs are subjected to a chemokine gradient, and their migratory response is evaluated. In the T cell compartment, rapid DC-induced activation of T cells is evaluated by measuring the level of calcium in T cells. We demonstrate the efficacy of our approach by evaluating the integrated response of mature DCs, whereby the overall T cell activation response is governed both by the chemotaxis and the T cell activation potential of mature DCs relative to immature DCs. Our system provides a powerful platform for systematically probing various aspects of antigen induced immune responses - DC maturation, migration and T cell activation - in an integrated fashion.
树突状细胞是主要的抗原呈递细胞,负责从外周组织获取并运输抗原至二级淋巴组织。在那里,它们将抗原呈递给T细胞,最终引发抗原特异性免疫反应。树突状细胞(DCs)的迁移与T细胞活化密切相关。然而,目前缺乏能够促进对DC趋化性以及迁移后的DC所导致的T细胞活化进行综合评估的系统。在这项工作中,我们开发了一种将DC趋化性与T细胞活化整合在一起的微制造平台。该微器件的基本设计包括两层聚二甲基硅氧烷(PDMS),顶层为趋化性隔室,底层为T细胞隔室。在趋化性隔室中,DCs受到趋化因子梯度的作用,并评估其迁移反应。在T细胞隔室中,通过测量T细胞中的钙水平来评估DC诱导的T细胞快速活化。我们通过评估成熟DCs的综合反应来证明我们方法的有效性,其中整体T细胞活化反应既受趋化性的影响,也受成熟DCs相对于未成熟DCs的T细胞活化潜能的影响。我们的系统提供了一个强大的平台,用于以综合方式系统地探究抗原诱导的免疫反应的各个方面——DC成熟、迁移和T细胞活化。