Tissue Eng Regen Med.  2020 Jun;17(3):301-311. 10.1007/s13770-020-00246-8.

Channeling Effect and Tissue Morphology in a Perfusion Bioreactor Imaged by X-Ray Microtomography

Affiliations
  • 1Lab. EM2C, UPR CNRS 288, CentraleSupe´lec, Universite´ Paris-Saclay, 3 rue Joliot-Curie, 91192 Gif-sur-Yvette Cedex, France
  • 2Lab. MSSMat, UMR CNRS 8579, CentraleSupe´lec, Universite´ Paris-Saclay, 3 rue Joliot-Curie, 91192 Gif-sur-Yvette Cedex, France
  • 3Single Molecule Biophotonics Lab. ICFO, The Institute of Photonic Sciences, av. Carl Friedrich Gauss, 3, 08860 Castelldefels, Barcelona, Spain
  • 4ENS Paris Saclay, LMT, CNRS, UMR 8535, 61 avenue du Pre´sident Wilson, 94230 Cachan, France
  • 5Institut Jacques Monod (IJM), UMR CNRS 7592, Universite´ Paris Diderot, 15 rue He´le`ne Brion, 75013 Paris, France

Abstract

BACKGROUND
Perfusion bioreactors for tissue engineering hold great promises. Indeed, the perfusion of culture medium enhances species transport and mechanically stimulates the cells, thereby increasing cell proliferation and tissue formation. Nonetheless, their development is still hampered by a lack of understanding of the relationship between mechanical cues and tissue growth.
METHODS
Combining tissue engineering, three-dimensional visualization and numerical simulations, we analyze the morphological evolution of neo-tissue in a model bioreactor with respect to the local flow pattern. NIH-3T3 cells were grown under perfusion for one, two and three weeks on a stack of 2 mm polyacetal beads. The model bioreactor was then imaged by X-ray micro-tomography and local tissue morphology was analyzed. To relate experimental observations and mechanical stimulii, a computational fluid dynamics model of flow around spheres in a canal was developed and solved using the finite element method.
RESULTS
We observe a preferential tissue formation at the bioreactor periphery, and relate it to a channeling effect leading to regions of higher flow intensity. Additionally, we find that circular crater-like tissue patterns form in narrow channel regions at early culture times. Using computational fluid dynamic simulations, we show that the location and morphology of these patterns match those of shear stress maxima. Finally, the morphology of the tissue is qualitatively described as the tissue grows and reorganizes itself.
CONCLUSION
Altogether, our study points out the key role of local flow conditions on the tissue morphology developed on a stack of beads in perfusion bioreactors and provides new insights for effective design of hydrodynamic bioreactors for tissue engineering using bead packings.

Keyword

X-ray microtomography; Perfusion bioreactor; Tissue engineering; Channeling effect; Tissue morphology
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