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SELECTBIO Conferences Organ-on-a-Chip and 3D-Culture: Companies, Technologies and Approaches

Michael Wong's Biography



Michael Wong, Researcher, Faculty of Health Sciences, McMaster University

Michael completed his BSc and MSc in Physiology and Pharmacology at Western University where he was recognized with the Best New Investigator Award, Graduate Student-of-the-Year, and top thesis submission. Michael is currently completing his PhD in Medical Sciences at McMaster University where he holds the Vanier Scholarship. Outside of the lab, he is passionate about cultivating Canada’s health sciences innovation and biotech sector, and thus founded an initiative known as Industry Link to better connect the gap from academia to industry.

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Extracellular Matrix Thickness Directs Self-Assembly, Function, and Gene Expression Profiles of Three-Dimensional Placental Trophoblast Spheroids

Tuesday, 11 July 2017 at 14:30

Add to Calendar ▼2017-07-11 14:30:002017-07-11 15:30:00Europe/LondonExtracellular Matrix Thickness Directs Self-Assembly, Function, and Gene Expression Profiles of Three-Dimensional Placental Trophoblast SpheroidsSELECTBIOenquiries@selectbiosciences.com

The incorporation of ECM is essential for generating in vitro placental models that better mimic the architecture and function found within human tissues. However, the appropriate utilization of laboratory-derived ECM biomaterials in placental trophoblast modelling remains poorly understood. In this study, we investigated the effect of varying thicknesses of two ECM surfaces, collagen I and Matrigel, on placental trophoblast cell morphology, proliferation, and gene and protein expression. In the current study, the effect of varying thicknesses of collagen I and Matrigel on BeWo placental trophoblast cell morphology, proliferation, and gene expression (differentiation, syncytial fusion, invasion/migration) were investigated. Matrigel, but not collagen I, induced self-organization of BeWo trophoblasts into three-dimensional spheroids that maintained for up to 21 days. Notably, it was revealed that a critical hydrogel surface thickness was required to induce spheroid formation. Trophoblast spheroids exhibited thickness-dependent increases proliferation and invasive gene expression profiles compared to two-dimensional cultures. Genes involved in syncytial fusion also exhibited thickness-dependent changes in expression. In consideration of the increased use of 3D bioprinting and dynamic model systems within the last several years, proper integration of ECM surfaces will be a crucial step towards creating more in vivo-like models. The generation of 3D, self-assembling spheroid cultures through regulation of ECM surface thickness alone further contributes to the development of more physiologically-relevant placental in vitro systems and innovative drug screening tools for pregnancy.


Add to Calendar ▼2017-07-10 00:00:002017-07-11 00:00:00Europe/LondonOrgan-on-a-Chip and 3D-Culture: Companies, Technologies and ApproachesSELECTBIOenquiries@selectbiosciences.com