High-Throughput Mechanobiology Screening Platform Using Micro- and Nanotopography

被引:40
作者
Hu, Junqiang [1 ]
Gondarenko, Alexander A. [1 ]
Dang, Alex P. [2 ]
Bashour, Keenan T. [2 ]
O'Connor, Roddy S. [5 ]
Lee, Sunwoo [3 ]
Liapis, Anastasia [6 ]
Ghassemi, Saba [5 ]
Milone, Michael C. [5 ]
Sheetz, Michael P. [4 ]
Dustin, Michael L. [7 ]
Kam, Lance C. [2 ]
Hone, James C. [1 ]
机构
[1] Columbia Univ, Dept Mech Engn, New York, NY 10027 USA
[2] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[3] Columbia Univ, Dept Elect Engn, New York, NY 10027 USA
[4] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[5] Univ Penn, Perelman Sch Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[6] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[7] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthoped Rheumatol & Musculoskeleta, Oxford OX3 7FY, England
基金
美国国家卫生研究院;
关键词
High-throughput screening; nanotechnology; T cell; interleukin-2; Lck; long-term expansion; T-CELL-ACTIVATION; SIGNAL-TRANSDUCTION; ACTIN POLYMERIZATION; EXTRACELLULAR-MATRIX; CD28; DIFFERENTIATION; PROLIFERATION; RECEPTOR; TOPOGRAPHY; MORPHOLOGY;
D O I
10.1021/acs.nanolett.5b04364
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We herein demonstrate the first 96-well plate platform to screen effects of micro- and nanotopographies on cell growth and proliferation. Existing high-throughput platforms test a limited number of factors and are not fully compatible with multiple types of testing and assays. This platform is compatible with high-throughput liquid handling, high-resolution imaging, and all multiwell plate-based instrumentation. We use the platform to screen for topographies and drug-topography combinations that have short and long-term effects on T cell activation and proliferation. We coated nanofabricated "trench-grid" surfaces with anti-CD3 and anti-CD28 antibodies to activate T cells and assayed for interleukin 2 (IL-2) cytokine production. IL-2 secretion was enhanced at 200 nm trench width and >2.3 mu m grating pitch; however, the secretion was suppressed at 100 nm width and <0.5 mu m pitch. The enhancement on 200 nm grid trench was further amplified with the addition of blebbistatin to reduce contractility. The 200 nm grid pattern was found to triple the number of T cells in long-term expansion, a result with direct clinical applicability in adoptive immunotherapy.
引用
收藏
页码:2198 / 2204
页数:7
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