Multiplexed Cell-Based Sensors for Assessing the Impact of Engineered Systems and Methods on Cell Health.

Bioinstrumentation engineers have long been creating platforms to study cell health and disease. It becomes necessary to ensure that such cell-probing tools do not themselves harm cells through complex stressors resulting from their design or operational conditions. Here, we present multiplexed cell-based sensors to simultaneously quantify stress induced by diverse mechanisms such as shear stress, DNA damage, and heat shock. Our sensors do not require additional reagents and can be conveniently quantified by flow cytometry and real-time imaging. Successful adaptation of our sensors by external users enabled systematic assessment of multiple flow sorters, alongside their operational parameters using the same cells and preparation. Our results provide insight into "gentle" and stressful sorting parameters that had not been quantified previously. Overall, this work presents a facile and quantitative approach to investigate multifactorial cell-stress emergent from diverse bioinstrumentation, which can be utilized to discover design and operation conditions ideal for cell health.

[1]  Hanry Yu,et al.  A practical guide to microfluidic perfusion culture of adherent mammalian cells. , 2007, Lab on a chip.

[2]  Ruo-Pan Huang,et al.  UV irradiation upregulates Egr‐1 expression at transcription level , 1999, Journal of cellular biochemistry.

[3]  D. Harrison,et al.  Methods for detection of mitochondrial and cellular reactive oxygen species. , 2014, Antioxidants & redox signaling.

[4]  Brendan D. Price,et al.  Sequential Phosphorylation by Mitogen-activated Protein Kinase and Glycogen Synthase Kinase 3 Represses Transcriptional Activation by Heat Shock Factor-1* , 1996, The Journal of Biological Chemistry.

[5]  Ron Taticek,et al.  Bioprocess Equipment: Characterization of Energy Dissipation Rate and Its Potential to Damage Cells , 2004, Biotechnology progress.

[6]  D. Beebe,et al.  Cell culture models in microfluidic systems. , 2008, Annual review of analytical chemistry.

[7]  Massimo Morbidelli,et al.  Determination of the maximum operating range of hydrodynamic stress in mammalian cell culture. , 2015, Journal of biotechnology.

[8]  V. Adler,et al.  UV Irradiation and Heat Shock Mediate JNK Activation via Alternate Pathways (*) , 1995, The Journal of Biological Chemistry.

[9]  Huaqiang Fang,et al.  Imaging ROS signaling in cells and animals , 2013, Journal of Molecular Medicine.

[10]  Ronan M. T. Fleming,et al.  Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices. , 2015, Biosensors & bioelectronics.

[11]  Joel Voldman,et al.  Cell-based sensors for quantifying the physiological impact of microsystems. , 2010, Integrative biology : quantitative biosciences from nano to macro.

[12]  J. Voldman,et al.  Microfluidic arrays for logarithmically perfused embryonic stem cell culture. , 2006, Lab on a chip.

[13]  R. Nilsson,et al.  Metabolite Profiling and Stable Isotope Tracing in Sorted Subpopulations of Mammalian Cells. , 2016, Analytical chemistry.

[14]  Jungmok You,et al.  Photodegradable hydrogels for capture, detection, and release of live cells. , 2014, Angewandte Chemie.

[15]  J. Chalmers,et al.  Flow parameters associated with hydrodynamic cell injury , 1994, Biotechnology and bioengineering.

[16]  V. Tron,et al.  Heat shock transcription factor-1 regulates heat shock protein-72 expression in human keratinocytes exposed to ultraviolet B light. , 1998, The Journal of investigative dermatology.

[17]  Kevin Burgess,et al.  Fluorescent indicators for intracellular pH. , 2010, Chemical reviews.

[18]  D. Lane,et al.  Oxidative stress is involved in the UV activation of p53. , 1996, Journal of cell science.

[19]  Cleo Kontoravdi,et al.  Genetically-encoded biosensors for monitoring cellular stress in bioprocessing. , 2015, Current opinion in biotechnology.

[20]  Ruben Godoy-Silva,et al.  Computer simulations of the energy dissipation rate in a fluorescence‐activated cell sorter: Implications to cells , 2008, Biotechnology and bioengineering.

[21]  Hans Lee,et al.  A cytotoxic leachable compound from single‐use bioprocess equipment that causes poor cell growth performance , 2014, Biotechnology progress.

[22]  O. Isacson,et al.  Markers and Methods for Cell Sorting of Human Embryonic Stem Cell‐Derived Neural Cell Populations , 2007, Stem cells.

[23]  G. Bao,et al.  Simultaneous detection of mRNA and protein stem cell markers in live cells , 2009, BMC biotechnology.

[24]  Jing Ge,et al.  Standard fluorescent imaging of live cells is highly genotoxic , 2013, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[25]  W. Earnshaw,et al.  Apoptosis-associated caspase activation assays. , 2008, Methods.

[26]  B. Wang,et al.  Arsenite induces premature senescence via p53/p21 pathway as a result of DNA damage in human malignant glioblastoma cells , 2014, BMB reports.

[27]  Joel Voldman,et al.  A cell-based sensor of fluid shear stress for microfluidics. , 2015, Lab on a chip.

[28]  A. Bhagat,et al.  Inertial microfluidics for continuous particle separation in spiral microchannels. , 2009, Lab on a chip.

[29]  Ruo-Pan Huang,et al.  Egr-1 inhibits apoptosis during the UV response: correlation of cell survival with Egr-1 phosphorylation , 1998, Cell Death and Differentiation.

[30]  George M. Church,et al.  CRISPR/Cas9‐Directed Genome Editing of Cultured Cells , 2014, Current protocols in molecular biology.

[31]  Jeffrey J. Chalmers,et al.  The potential of hydrodynamic damage to animal cells of industrial relevance: current understanding , 2011, Cytotechnology.

[32]  P. Black,et al.  Continuous Flow Deformability-Based Separation of Circulating Tumor Cells Using Microfluidic Ratchets. , 2016, Small.

[33]  J. C. Love,et al.  Stochastic particle barcoding for single-cell tracking and multiparametric analysis. , 2014, Small.

[34]  M. Simon,et al.  Heat shock protein 70 overexpression affects the response to ultraviolet light in murine fibroblasts. Evidence for increased cell viability and suppression of cytokine release. , 1995, The Journal of clinical investigation.

[35]  Jianghong Rao,et al.  Real-time imaging of oxidative and nitrosative stress in the liver of live animals for drug-toxicity testing , 2014, Nature Biotechnology.

[36]  Joel Voldman,et al.  Cell-Based Biosensor to Report DNA Damage in Micro- and Nanosystems , 2014, Analytical chemistry.

[37]  E. Adamson,et al.  A biological role for Egr-1 in cell survival following ultra-violet irradiation. , 1995, Oncogene.

[38]  Joanne Lannigan,et al.  Does FACS perturb gene expression? , 2015, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

[39]  R. Tompkins,et al.  Continuous inertial focusing, ordering, and separation of particles in microchannels , 2007, Proceedings of the National Academy of Sciences.

[40]  Majid Ebrahimi Warkiani,et al.  Flow-induced stress on adherent cells in microfluidic devices. , 2015, Lab on a chip.

[41]  Nicole K Henderson-Maclennan,et al.  Deformability-based cell classification and enrichment using inertial microfluidics. , 2011, Lab on a chip.

[42]  David K. Wood,et al.  Single cell trapping and DNA damage analysis using microwell arrays , 2010, Proceedings of the National Academy of Sciences.

[43]  R. Okayasu,et al.  Induction of DNA double strand breaks by arsenite: comparative studies with DNA breaks induced by X-rays. , 2003, DNA repair.