TY - JOUR
T1 - Design and Evaluation of an Osteogenesis-on-a-Chip Microfluidic Device Incorporating 3D Cell Culture
AU - Bahmaee, Hossein
AU - Owen, Robert
AU - Boyle, Liam
AU - Perrault, Cecile M.
AU - Garcia-Granada, Andres A.
AU - Reilly, Gwendolen C.
AU - Claeyssens, Frederik
N1 - Funding Information:
We acknowledge funding from the Engineering and Physical Sciences Research Council (Grant Nos. EP/N509735/1 and
Funding Information:
Funding. We acknowledge funding from the Engineering and Physical Sciences Research Council (Grant Nos. EP/N509735/1 and EP/L505055/1) and Biotechnology and Biological Sciences Research Council (Grant No. BB/F016840/1) for studentships for RO and LB. We also acknowledge the EPSRC Henry Royce Institute funding (Grant No. EP/P02470X/1) for the light sheet microscope, and funding from the EPSRC (Grant No. EP/I007695/1) and the Medical Research Council (MR/L012669/1) for establishing the laser laboratory. Confocal imaging was performed at the Kroto Imaging Facility.
Publisher Copyright:
© Copyright © 2020 Bahmaee, Owen, Boyle, Perrault, Garcia-Granada, Reilly and Claeyssens.
PY - 2020/9/8
Y1 - 2020/9/8
N2 - Microfluidic-based tissue-on-a-chip devices have generated significant research interest for biomedical applications, such as pharmaceutical development, as they can be used for small volume, high throughput studies on the effects of therapeutics on tissue-mimics. Tissue-on-a-chip devices are evolving from basic 2D cell cultures incorporated into microfluidic devices to complex 3D approaches, with modern designs aimed at recapitulating the dynamic and mechanical environment of the native tissue. Thus far, most tissue-on-a-chip research has concentrated on organs involved with drug uptake, metabolism and removal (e.g., lung, skin, liver, and kidney); however, models of the drug metabolite target organs will be essential to provide information on therapeutic efficacy. Here, we develop an osteogenesis-on-a-chip device that comprises a 3D environment and fluid shear stresses, both important features of bone. This inexpensive, easy-to-fabricate system based on a polymerized High Internal Phase Emulsion (polyHIPE) supports proliferation, differentiation and extracellular matrix production of human embryonic stem cell-derived mesenchymal progenitor cells (hES-MPs) over extended time periods (up to 21 days). Cells respond positively to both chemical and mechanical stimulation of osteogenesis, with an intermittent flow profile containing rest periods strongly promoting differentiation and matrix formation in comparison to static and continuous flow. Flow and shear stresses were modeled using computational fluid dynamics. Primary cilia were detectable on cells within the device channels demonstrating that this mechanosensory organelle is present in the complex 3D culture environment. In summary, this device aids the development of ‘next-generation’ tools for investigating novel therapeutics for bone in comparison with standard laboratory and animal testing.
AB - Microfluidic-based tissue-on-a-chip devices have generated significant research interest for biomedical applications, such as pharmaceutical development, as they can be used for small volume, high throughput studies on the effects of therapeutics on tissue-mimics. Tissue-on-a-chip devices are evolving from basic 2D cell cultures incorporated into microfluidic devices to complex 3D approaches, with modern designs aimed at recapitulating the dynamic and mechanical environment of the native tissue. Thus far, most tissue-on-a-chip research has concentrated on organs involved with drug uptake, metabolism and removal (e.g., lung, skin, liver, and kidney); however, models of the drug metabolite target organs will be essential to provide information on therapeutic efficacy. Here, we develop an osteogenesis-on-a-chip device that comprises a 3D environment and fluid shear stresses, both important features of bone. This inexpensive, easy-to-fabricate system based on a polymerized High Internal Phase Emulsion (polyHIPE) supports proliferation, differentiation and extracellular matrix production of human embryonic stem cell-derived mesenchymal progenitor cells (hES-MPs) over extended time periods (up to 21 days). Cells respond positively to both chemical and mechanical stimulation of osteogenesis, with an intermittent flow profile containing rest periods strongly promoting differentiation and matrix formation in comparison to static and continuous flow. Flow and shear stresses were modeled using computational fluid dynamics. Primary cilia were detectable on cells within the device channels demonstrating that this mechanosensory organelle is present in the complex 3D culture environment. In summary, this device aids the development of ‘next-generation’ tools for investigating novel therapeutics for bone in comparison with standard laboratory and animal testing.
KW - additive manufacture
KW - bioreactor
KW - computational fluid dynamics
KW - mechanotransduction
KW - organ-on-a-chip
KW - polyHIPE
KW - tissue engineering
UR - http://www.scopus.com/inward/record.url?scp=85091435889&partnerID=8YFLogxK
U2 - 10.3389/fbioe.2020.557111
DO - 10.3389/fbioe.2020.557111
M3 - Article
AN - SCOPUS:85091435889
SN - 2296-4185
VL - 8
JO - Frontiers in Bioengineering and Biotechnology
JF - Frontiers in Bioengineering and Biotechnology
M1 - 557111
ER -