| Literature DB >> 26990380 |
Junqiang Hu, Alexander A Gondarenko, Alex P Dang, Keenan T Bashour, Roddy S O'Connor1, Sunwoo Lee, Anastasia Liapis2, Saba Ghassemi1, Michael C Milone1, Michael P Sheetz, Michael L Dustin3, Lance C Kam, James C Hone.
Abstract
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 μm grating pitch; however, the secretion was suppressed at 100 nm width and <0.5 μm 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.Entities:
Keywords: High-throughput screening; Lck; T cell; interleukin-2; long-term expansion; nanotechnology
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Year: 2016 PMID: 26990380 PMCID: PMC5403373 DOI: 10.1021/acs.nanolett.5b04364
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189