A rapid co-culture stamping device for studying intercellular communication

被引:0
作者
Amin Hassanzadeh-Barforoushi
Jonathan Shemesh
Nona Farbehi
Mohsen Asadnia
Guan Heng Yeoh
Richard P. Harvey
Robert E. Nordon
Majid Ebrahimi Warkiani
机构
[1] School of Mechanical and Manufacturing Engineering,Department of Engineering
[2] University of New South Wales,Developmental and Stem Cell Biology Division
[3] Graduate School of Biomedical Engineering,undefined
[4] University of New South Wales,undefined
[5] Faculty of Science,undefined
[6] Macquarie University,undefined
[7] Victor Chang Cardiac Research Institute,undefined
[8] Sydney,undefined
[9] NSW,undefined
[10] 2010; St. Vincent’s Clinical School and School of Biotechnology and Biomolecular Science,undefined
[11] University of New South Wales,undefined
[12] Australian Centre for Nanomedicine,undefined
[13] University of New South Wales,undefined
[14] Sydney,undefined
[15] NSW 2052,undefined
[16] Australia; Garvan Institute of Medical Research,undefined
[17] Darlinghurst,undefined
[18] School of Medical Sciences,undefined
[19] Edith Cowan University,undefined
来源
Scientific Reports | / 6卷
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摘要
Regulation of tissue development and repair depends on communication between neighbouring cells. Recent advances in cell micro-contact printing and microfluidics have facilitated the in-vitro study of homotypic and heterotypic cell-cell interaction. Nonetheless, these techniques are still complicated to perform and as a result, are seldom used by biologists. We report here development of a temporarily sealed microfluidic stamping device which utilizes a novel valve design for patterning two adherent cell lines with well-defined interlacing configurations to study cell-cell interactions. We demonstrate post-stamping cell viability of >95%, the stamping of multiple adherent cell types, and the ability to control the seeded cell density. We also show viability, proliferation and migration of cultured cells, enabling analysis of co-culture boundary conditions on cell fate. We also developed an in-vitro model of endothelial and cardiac stem cell interactions, which are thought to regulate coronary repair after myocardial injury. The stamp is fabricated using microfabrication techniques, is operated with a lab pipettor and uses very low reagent volumes of 20 μl with cell injection efficiency of >70%. This easy-to-use device provides a general strategy for micro-patterning of multiple cell types and will be important for studying cell-cell interactions in a multitude of applications.
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