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Chiappini, C.

Publications and source records attributed to Chiappini, C..

2 recordsLinked to original sources

Axonal length determines distinct homeostatic phenotypes in human iPSC derived motor neurons on a bioengineered platform

Stem cell-based experimental platforms for neuroscience can effectively model key mechanistic aspects of human development and disease. However, conventional culture systems often overlook the engineering constraints that cells face in vivo. This is particularly relevant for neurons covering long range connections such as spinal motor neurons (MNs). The axons of these neurons extend up to 1m in length and require a complex interplay of mechanisms to maintain cellular homeostasis. It follows that shorter axons in conventional cultures may not faithfully capture important aspects of their longer counterparts. Here we directly address this issue by establishing a bioengineered platform to assemble arrays of human axons ranging from micrometers to centimeters, permitting systematic investigation of the effects of length on human axonal biology for the first time. With this approach, we reveal a link between length and metabolism in human MNs in vitro, where axons above a "threshold" size induce specific molecular adaptations in cytoskeleton composition, functional properties, local translation and mitochondrial homeostasis. Our findings specifically demonstrate the existence of a length-dependent mechanism that switches homeostatic processes within human MNs in order to sustain long axons. Our findings have critical implications for in vitro modelling of several neurodegenerative disorders and reinforce the importance of modelling cell shape and biophysical constraints with fidelity and precision in vitro.

neuroscience↗

Epicardial slices: a 3D organotypic model for the study of epicardial activation and differentiation

The epicardium constitutes an untapped reservoir for cardiac regeneration. Upon myocardial injury, the adult epicardium re-activates the embryonic program, leading to epithelial-to-mesenchymal transition, migration and differentiation. Despite some successes in harnessing the epicardial therapeutic potential by thymosin {beta}4 (T{beta}4) pre-treatment, further translational advancements are hampered by the paucity of representative experimental models. Here we apply innovative protocols to obtain living 3D organotypic slices from porcine hearts, encompassing the epicardial/myocardial interface. In culture, our slices preserve the in vivo architecture and functionality, presenting a continuous epicardium overlaying a healthy and connected myocardium. Upon T{beta}4 treatment of the slices, the epicardial cells become activated upregulating embryonic and EMT genes and invading the myocardium where they differentiate towards the mesenchymal lineage. Our 3D organotypic model enables to investigate the reparative potential of the adult epicardium, offering a new tool to explore ex vivo the complex 3D interactions occurring within the native heart environment.

bioengineering↗