Breast on-a-chip: mimicry of the channeling system of the breast for development of theranostics.

Improved detection and therapy of breast neoplasia might benefit from nanodevices traveling inside mammary ducts. However, the decreasing size of branched mammary ducts prevents access to remote areas of the ductal system using a pressure-driven fluid-based approach. Magnetic field guidance of superparamagnetic submicron particles (SMPs) in a stationary fluid might provide a possible alternative but it is critical to first reproduce the breast ductal system to assess the use of such devices for future therapeutic & diagnostic ("theranostic") purposes. Here we describe the engineering of a portion of a breast ductal system using polydimethylsiloxane (PDMS) microfluidic channels with a total volume of 0.09 μl. A magnet was used to move superparamagnetic/fluorescent SMPs through a static fluid inside the microchannels. Non-neoplastic mammary epithelial S1 cells developed basoapical polarity as a flat monolayer on the PDMS surface when cultured in the presence of laminin 111, and incubation with SMPs did not result in detectable toxicity. Cells could not withstand the fluid pressure if microinjected directly in completed channels. Whereas, they readily covered laminin 111-coated PDMS surfaces when cultured in U-shaped "hemichannels" before completing the channels. This breast-on-chip model represents a critical step towards the mimicry of the tree-like ductal system of the breast for further testing and targeting of SMPs.

[1]  M J Bissell,et al.  Tissue phenotype depends on reciprocal interactions between the extracellular matrix and the structural organization of the nucleus. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[2]  Christopher B Umbricht,et al.  Detection of breast cancer cells in ductal lavage fluid by methylation-specific PCR , 2001, The Lancet.

[3]  Elena F. Brachtel,et al.  Breast duct anatomy in the human nipple: three-dimensional patterns and clinical implications , 2007, Breast Cancer Research and Treatment.

[4]  D. Leslie-Pelecky,et al.  Biodistribution, clearance, and biocompatibility of iron oxide magnetic nanoparticles in rats. , 2008, Molecular pharmaceutics.

[5]  A. Fischer,et al.  The ultrastructure of MCF‐10A acini , 2006, Journal of cellular physiology.

[6]  Technical Enhancements to Breast Ductal Lavage , 2008, Annals of Surgical Oncology.

[7]  J. Sturgis,et al.  Factors necessary to produce basoapical polarity in human glandular epithelium formed in conventional and high-throughput three-dimensional culture: example of the breast epithelium , 2009, BMC Biology.

[8]  Carlos Sonnenschein,et al.  The role of collagen reorganization on mammary epithelial morphogenesis in a 3D culture model. , 2010, Biomaterials.

[9]  D. Kaplan,et al.  A complex 3D human tissue culture system based on mammary stromal cells and silk scaffolds for modeling breast morphogenesis and function. , 2010, Biomaterials.

[10]  Hanry Yu,et al.  A novel 3D mammalian cell perfusion-culture system in microfluidic channels. , 2007, Lab on a chip.

[11]  B. Margolis,et al.  Multiple regions of Crumbs3 are required for tight junction formation in MCF10A cells , 2005, Journal of Cell Science.

[12]  G. Whitesides,et al.  Rapid Prototyping of Microfluidic Systems in Poly(dimethylsiloxane). , 1998, Analytical chemistry.

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

[14]  R. Eeles,et al.  Ductal approaches to assessment and management of women at high risk for developing breast cancer , 2004, Breast Cancer Research.

[15]  O. Petersen,et al.  A new diploid nontumorigenic human breast epithelial cell line isolated and propagated in chemically defined medium , 1987, In Vitro Cellular & Developmental Biology.

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

[17]  Mina J Bissell,et al.  To create the correct microenvironment: three-dimensional heterotypic collagen assays for human breast epithelial morphogenesis and neoplasia. , 2003, Methods.

[18]  M. Bissell,et al.  Epimorphin Functions as a Key Morphoregulator for Mammary Epithelial Cells , 1998, The Journal of cell biology.

[19]  S. Fuller,et al.  Vesicular stomatitis virus infects and matures only through the basolateral surface of the polarized epithelial cell line, MDCK , 1984, Cell.

[20]  Sanford H Barsky,et al.  Anatomy of the nipple and breast ducts revisited , 2004, Cancer.