Cell Aggregate Assembly through Microengineering for Functional Tissue Emergence
Gozde Eke,
Laurence Vaysse,
Xi Yao,
Mélanie Escudero,
Audrey Carrière,
Emmanuelle Trevisiol,
Christophe Vieu,
Christian Dani,
Louis Casteilla,
Laurent Malaquin
Affiliations
Gozde Eke
Laboratoire d’Analyse et d’Architecture des Systèmes, Centre National de la Recherche Scientifique (LAAS-CNRS), Université de Toulouse, INSA, UPS, 31400 Toulouse, France
Laurence Vaysse
RESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, EFS, ENVT, 31100 Toulouse, France
Xi Yao
Institut de Biologie Valrose, Université Côte d’Azur, 06108 Nice, France
Mélanie Escudero
RESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, EFS, ENVT, 31100 Toulouse, France
Audrey Carrière
RESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, EFS, ENVT, 31100 Toulouse, France
Emmanuelle Trevisiol
Laboratoire d’Analyse et d’Architecture des Systèmes, Centre National de la Recherche Scientifique (LAAS-CNRS), Université de Toulouse, INSA, UPS, 31400 Toulouse, France
Christophe Vieu
Laboratoire d’Analyse et d’Architecture des Systèmes, Centre National de la Recherche Scientifique (LAAS-CNRS), Université de Toulouse, INSA, UPS, 31400 Toulouse, France
Christian Dani
Institut de Biologie Valrose, Université Côte d’Azur, 06108 Nice, France
Louis Casteilla
RESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, EFS, ENVT, 31100 Toulouse, France
Laurent Malaquin
Laboratoire d’Analyse et d’Architecture des Systèmes, Centre National de la Recherche Scientifique (LAAS-CNRS), Université de Toulouse, INSA, UPS, 31400 Toulouse, France
Compared to cell suspensions or monolayers, 3D cell aggregates provide cellular interactions organized in space and heterogeneity that better resume the real organization of native tissues. They represent powerful tools to narrow down the gap between in vitro and in vivo models, thanks to their self-evolving capabilities. Recent strategies have demonstrated their potential as building blocks to generate microtissues. Developing specific methodologies capable of organizing these cell aggregates into 3D architectures and environments has become essential to convert them into functional microtissues adapted for regenerative medicine or pharmaceutical screening purposes. Although the techniques for producing individual cell aggregates have been on the market for over a decade, the methodology for engineering functional tissues starting from them is still a young and quickly evolving field of research. In this review, we first present a panorama of emerging cell aggregates microfabrication and assembly technologies. We further discuss the perspectives opened in the establishment of functional tissues with a specific focus on controlled architecture and heterogeneity to favor cell differentiation and proliferation.