High-Throughput Mechanobiology Screening Platform Using Micro- and Nanotopography.

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.

[1]  Alexander Babich,et al.  F-actin polymerization and retrograde flow drive sustained PLCγ1 signaling during T cell activation , 2012, The Journal of cell biology.

[2]  Wei Wang,et al.  Flow-through functionalized PDMS microfluidic channels with dextran derivative for ELISAs. , 2009, Lab on a chip.

[3]  E. Sausville,et al.  Jasplakinolide, a cytotoxic natural product, induces actin polymerization and competitively inhibits the binding of phalloidin to F-actin. , 1994, The Journal of biological chemistry.

[4]  Lotte Markert,et al.  Identification of distinct topographical surface microstructures favoring either undifferentiated expansion or differentiation of murine embryonic stem cells. , 2009, Stem cells and development.

[5]  Patrik Schmuki,et al.  Nanoscale engineering of biomimetic surfaces: cues from the extracellular matrix , 2009, Cell and Tissue Research.

[6]  Lance C Kam,et al.  Micropatterning of costimulatory ligands enhances CD4+ T cell function , 2008, Proceedings of the National Academy of Sciences.

[7]  S. Haskill,et al.  Signal transduction from the extracellular matrix , 1993, The Journal of cell biology.

[8]  Yoon-Kyoung Cho,et al.  Investigation on the mechanism of aminosilane-mediated bonding of thermoplastics and poly(dimethylsiloxane). , 2012, ACS applied materials & interfaces.

[9]  Omer Dushek,et al.  Constitutively Active Lck Kinase in T Cells Drives Antigen Receptor Signal Transduction , 2010, Immunity.

[10]  N. Kotov,et al.  Three-dimensional cell culture matrices: state of the art. , 2008, Tissue engineering. Part B, Reviews.

[11]  Wilhelm Friedrich,et al.  Lymphocyte microvilli are dynamic, actin-dependent structures that do not require Wiskott-Aldrich syndrome protein (WASp) for their morphology , 2004 .

[12]  Anne E Carpenter,et al.  An algorithm-based topographical biomaterials library to instruct cell fate , 2011, Proceedings of the National Academy of Sciences.

[13]  Michael Loran Dustin,et al.  T Cell Activation is Determined by the Number of Presented Antigens , 2013, Nano letters.

[14]  P. Reynolds,et al.  A dual gradient assay for the parametric analysis of cell-surface interactions. , 2012, Small.

[15]  A. Trickett,et al.  T cell stimulation and expansion using anti-CD3/CD28 beads. , 2003, Journal of immunological methods.

[16]  M. Connors,et al.  Effects of CD28 costimulation on long-term proliferation of CD4+ T cells in the absence of exogenous feeder cells. , 1997, Journal of immunology.

[17]  L. Samelson,et al.  Dynamic actin polymerization drives T cell receptor-induced spreading: a role for the signal transduction adaptor LAT. , 2001, Immunity.

[18]  Michael Loran Dustin,et al.  Cross Talk between CD3 and CD28 Is Spatially Modulated by Protein Lateral Mobility , 2013, Molecular and Cellular Biology.

[19]  Michael Loran Dustin,et al.  Nanoengineering of Immune Cell Function. , 2009, Materials Research Society symposia proceedings. Materials Research Society.

[20]  C. Wilkinson,et al.  The control of human mesenchymal cell differentiation using nanoscale symmetry and disorder. , 2007, Nature materials.

[21]  Mark W. Tibbitt,et al.  Hydrogels as extracellular matrix mimics for 3D cell culture. , 2009, Biotechnology and bioengineering.

[22]  Lance C Kam,et al.  CD28 and CD3 have complementary roles in T-cell traction forces , 2014, Proceedings of the National Academy of Sciences.

[23]  Daniel I. C. Wang,et al.  Engineering cell shape and function. , 1994, Science.

[24]  Wayne W. Hancock,et al.  Substrate Rigidity Regulates Human T Cell Activation and Proliferation , 2012, The Journal of Immunology.

[25]  C. S. Chen,et al.  Geometric control of cell life and death. , 1997, Science.

[26]  Robert Langer,et al.  Biodegradable Polymer Scaffolds for Tissue Engineering , 1994, Bio/Technology.

[27]  Sudha Kumari,et al.  Immunology: Dendritic Cells Pull the T Cell’s Strings , 2015, Current Biology.

[28]  Z. Werb ECM and Cell Surface Proteolysis: Regulating Cellular Ecology , 1997, Cell.

[29]  Dan R. Littman,et al.  Signal transduction by lymphocyte antigen receptors , 1994, Cell.

[30]  R. Langer,et al.  Engineering substrate topography at the micro- and nanoscale to control cell function. , 2009, Angewandte Chemie.

[31]  David Allman,et al.  Ex vivo expansion of polyclonal and antigen-specific cytotoxic T lymphocytes by artificial APCs expressing ligands for the T-cell receptor, CD28 and 4-1BB , 2002, Nature Biotechnology.

[32]  G. Koretzky,et al.  T cell activation. , 2009, Annual review of immunology.

[33]  Kam W Leong,et al.  Synthetic nanostructures inducing differentiation of human mesenchymal stem cells into neuronal lineage. , 2007, Experimental cell research.

[34]  C J Murphy,et al.  Effects of synthetic micro- and nano-structured surfaces on cell behavior. , 1999, Biomaterials.

[35]  M. Moser Faculty Opinions recommendation of Polarized release of T-cell-receptor-enriched microvesicles at the immunological synapse. , 2014 .

[36]  Arthur Weiss,et al.  Function of the Src-family kinases, Lck and Fyn, in T-cell development and activation , 2004, Oncogene.

[37]  David L. Stokes,et al.  Polarized release of TCR-enriched microvesicles at the T cell immunological synapse , 2014, Nature.

[38]  G. Zhu,et al.  B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin-10 secretion , 1999, Nature Medicine.

[39]  S. Dzik B7-H1, a third member of the B7 family, co-stimulates T-cell proliferation and interleukin 10 secretion , 2000 .

[40]  L Ploux,et al.  The interaction of cells and bacteria with surfaces structured at the nanometre scale. , 2010, Acta biomaterialia.

[41]  Kam W Leong,et al.  Nanopattern-induced changes in morphology and motility of smooth muscle cells. , 2005, Biomaterials.

[42]  M. Sheetz,et al.  Microarray with micro- and nano-topographies enables identification of the optimal topography for directing the differentiation of primary murine neural progenitor cells. , 2012, Small.

[43]  Michael L. Dustin,et al.  New insights into the T cell synapse from single molecule techniques , 2011, Nature Reviews Immunology.

[44]  R. G. Richards,et al.  Nanotopographical modification: a regulator of cellular function through focal adhesions. , 2010, Nanomedicine : nanotechnology, biology, and medicine.

[45]  Timothy J Mitchison,et al.  Dissecting Temporal and Spatial Control of Cytokinesis with a Myosin II Inhibitor , 2003, Science.

[46]  K. Takase,et al.  [T cell activation]. , 1995, Ryumachi. [Rheumatism].