Surface-tension driven open microfluidic platform for hanging droplet culture.

The hanging droplet technique for three-dimensional tissue culture has been used for decades in biology labs, with the core technology remaining relatively unchanged. Recently microscale approaches have expanded the capabilities of the hanging droplet method, making it more user-friendly. We present a spontaneously driven, open hanging droplet culture platform to address many limitations of current platforms. Our platform makes use of two interconnected hanging droplet wells, a larger well where cells are cultured and a smaller well for user interface via a pipette. The two-well system results in lower shear stress in the culture well during fluid exchange, enabling shear sensitive or non-adherent cells to be cultured in a droplet. The ability to perform fluid exchanges in-droplet enables long-term culture, treatment, and characterization without disruption of the culture. The open well format of the platform was utilized to perform time-dependent coculture, enabling culture configurations with bone tissue scaffolds and cells grown in suspension. The open nature of the system allowed the direct addition or removal of tissue over the course of an experiment, manipulations that would be impractical in other microfluidic or hanging droplet culture platforms.

[1]  Heinz Schmid,et al.  Continuous flow in open microfluidics using controlled evaporation. , 2005, Lab on a chip.

[2]  Xiaotong Hu,et al.  Down-Regulation of CD9 by Methylation Decreased Bortezomib Sensitivity in Multiple Myeloma , 2014, PloS one.

[3]  T. Kipps,et al.  CXCR4: a key receptor in the crosstalk between tumor cells and their microenvironment. , 2006, Blood.

[4]  D. Beebe,et al.  Physics and applications of microfluidics in biology. , 2002, Annual review of biomedical engineering.

[5]  Eric R. Prossnitz,et al.  A Transmembrane Intracellular Estrogen Receptor Mediates Rapid Cell Signaling , 2005, Science.

[6]  A. Belldegrun,et al.  Novel therapeutic strategies for castration resistant prostate cancer: inhibition of persistent androgen production and androgen receptor mediated signaling. , 2011, The Journal of urology.

[7]  Juergen Friedrich,et al.  Spheroid-based drug screen: considerations and practical approach , 2009, Nature Protocols.

[8]  E. Richards,et al.  Pathobiology , 2015, Laboratory Investigation.

[9]  Emmanuel Delamarche,et al.  Microfluidics in the "open space" for performing localized chemistry on biological interfaces. , 2012, Angewandte Chemie.

[10]  D. Kaplan,et al.  Investigating osteogenic differentiation in multiple myeloma using a novel 3D bone marrow niche model. , 2014, Blood.

[11]  David J Beebe,et al.  Managing evaporation for more robust microscale assays. Part 2. Characterization of convection and diffusion for cell biology. , 2008, Lab on a chip.

[12]  G. G. Stokes "J." , 1890, The New Yale Book of Quotations.

[13]  R. Nerem,et al.  Altered response of vascular smooth muscle cells to exogenous biochemical stimulation in two- and three-dimensional culture. , 2003, Experimental cell research.

[14]  David J Beebe,et al.  Micromilling: a method for ultra-rapid prototyping of plastic microfluidic devices. , 2015, Lab on a chip.

[15]  A. Janorkar,et al.  A surface‐tethered spheroid model for functional evaluation of 3T3‐L1 adipocytes , 2014, Biotechnology and bioengineering.

[16]  Luke P. Lee,et al.  Microfluidic self-assembly of tumor spheroids for anticancer drug discovery , 2008, Biomedical microdevices.

[17]  U. N. Joensen,et al.  Hanging drop cultures of human testis and testis cancer samples: a model used to investigate activin treatment effects in a preserved niche , 2014, British Journal of Cancer.

[18]  Robert Langer,et al.  Preparation and characterization of poly(l-lactic acid) foams , 1994 .

[19]  Shuichi Takayama,et al.  High-throughput 3D spheroid culture and drug testing using a 384 hanging drop array. , 2011, The Analyst.

[20]  Wan-Wan Lin,et al.  A cytokine-mediated link between innate immunity, inflammation, and cancer. , 2007, The Journal of clinical investigation.

[21]  Shuichi Takayama,et al.  Microfluidic system for formation of PC-3 prostate cancer co-culture spheroids. , 2009, Biomaterials.

[22]  I. Ghobrial,et al.  Multiple Myeloma Mesenchymal Stem Cells: Characterization, Origin, and Tumor-Promoting Effects , 2011, Clinical Cancer Research.

[23]  T. Libermann,et al.  Multiple myeloma cell adhesion-induced interleukin-6 expression in bone marrow stromal cells involves activation of NF-kappa B. , 1996, Blood.

[24]  Charles P. Lin,et al.  CXCR4 inhibitor AMD3100 disrupts the interaction of multiple myeloma cells with the bone marrow microenvironment and enhances their sensitivity to therapy. , 2009, Blood.

[25]  Andreas Hierlemann,et al.  Reconfigurable microfluidic hanging drop network for multi-tissue interaction and analysis , 2014, Nature Communications.

[26]  N. Mechti,et al.  Extracellular matrix in bone marrow can mediate drug resistance in myeloma , 2005, Leukemia & lymphoma.

[27]  J. Frangos,et al.  The shear stress of it all: the cell membrane and mechanochemical transduction , 2007, Philosophical Transactions of the Royal Society B: Biological Sciences.

[28]  D. Chauhan,et al.  Characterization of the MM.1 human multiple myeloma (MM) cell lines: a model system to elucidate the characteristics, behavior, and signaling of steroid-sensitive and -resistant MM cells. , 2003, Experimental hematology.

[29]  C. Arrieumerlou,et al.  Cell-cell propagation of NF-κB transcription factor and MAP kinase activation amplifies innate immunity against bacterial infection. , 2010, Immunity.

[30]  David J Beebe,et al.  Flow rate analysis of a surface tension driven passive micropump. , 2007, Lab on a chip.

[31]  David J Beebe,et al.  Suspended microfluidics , 2013, Proceedings of the National Academy of Sciences.

[32]  H. Guillou,et al.  Spatial organization of the extracellular matrix regulates cell–cell junction positioning , 2012, Proceedings of the National Academy of Sciences.

[33]  N. Munshi,et al.  NF-κB as a Therapeutic Target in Multiple Myeloma* , 2002, The Journal of Biological Chemistry.

[34]  Shuichi Takayama,et al.  Micro-ring structures stabilize microdroplets to enable long term spheroid culture in 384 hanging drop array plates , 2011, Biomedical Microdevices.

[35]  Charles P. Lin,et al.  Mechanisms of regulation of CXCR4/SDF-1 (CXCL12)-dependent migration and homing in multiple myeloma. , 2007, Blood.

[36]  R. Seger,et al.  Identification and characterization of a general nuclear translocation signal in signaling proteins. , 2008, Molecular cell.

[37]  B. Dörken,et al.  In the presence of bone marrow stromal cells human multiple myeloma cells become independent of the IL-6/gp130/STAT3 pathway. , 2002, Blood.

[38]  Dong Yun Lee,et al.  In situ formation and collagen-alginate composite encapsulation of pancreatic islet spheroids. , 2012, Biomaterials.

[39]  L. A. Sandholzer,et al.  The Use of Semi-solid Agar for the Detection of Bacterial Motility , 1936, Journal of bacteriology.

[40]  M. Nehls,et al.  Shear stress inhibits apoptosis of human endothelial cells , 1996, FEBS letters.

[41]  H. Pahl Activators and target genes of Rel/NF-κB transcription factors , 1999, Oncogene.

[42]  Kimiko Yamamoto,et al.  Proliferation, differentiation, and tube formation by endothelial progenitor cells in response to shear stress. , 2003, Journal of applied physiology.

[43]  G D Roodman,et al.  Biology of osteoclast activation in cancer. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[44]  Jayanta Debnath,et al.  Morphogenesis and oncogenesis of MCF-10A mammary epithelial acini grown in three-dimensional basement membrane cultures. , 2003, Methods.

[45]  D H Kohn,et al.  Growth of continuous bonelike mineral within porous poly(lactide-co-glycolide) scaffolds in vitro. , 2000, Journal of biomedical materials research.

[46]  J. Folkman,et al.  SELF-REGULATION OF GROWTH IN THREE DIMENSIONS , 1973, The Journal of experimental medicine.

[47]  N. Munshi,et al.  Role of B-cell-activating factor in adhesion and growth of human multiple myeloma cells in the bone marrow microenvironment. , 2006, Cancer research.

[48]  A. C. Hildebrandt,et al.  THE PREPARATION, ISOLATION, AND GROWTH IN CULTURE OF SINGLE CELLS FROM HIGHER PLANTS , 1958 .

[49]  A. Abbott Cell culture: Biology's new dimension , 2003, Nature.

[50]  David J Beebe,et al.  Microscale functional cytomics for studying hematologic cancers. , 2012, Blood.

[51]  K. Shull,et al.  Mechanics of pendant drops and axisymmetric membranes , 2011 .

[52]  E. Cuppen,et al.  Identification of Multipotent Luminal Progenitor Cells in Human Prostate Organoid Cultures , 2014, Cell.

[53]  D. Beebe,et al.  Pipette-friendly laminar flow patterning for cell-based assays. , 2011, Lab on a chip.

[54]  David J Beebe,et al.  A passive pumping method for microfluidic devices. , 2002, Lab on a chip.

[55]  S. Plon,et al.  Bortezomib interactions with chemotherapy agents in acute leukemia in vitro , 2006, Cancer Chemotherapy and Pharmacology.

[56]  T. Paíno,et al.  Phenotypic, Genomic and Functional Characterization Reveals No Differences between CD138++ and CD138low Subpopulations in Multiple Myeloma Cell Lines , 2014, PloS one.

[57]  P. Richardson,et al.  The role of tumor necrosis factor α in the pathophysiology of human multiple myeloma: therapeutic applications , 2001, Oncogene.

[58]  E. Hurt,et al.  The role of IL-6 and STAT3 in inflammation and cancer. , 2005, European journal of cancer.