lecce.tecnomedpuglia

Abstract

Engineered microvessel stained for ZO-1 (green) and counterstained for nuclei (blue).

Cerebral vasculogenesis and angiogenesis are key processes in brain development and disease. However, traditional in vitro models fail to replicate the dynamic microenvironment that regulates vascular responses. This project aims to develop a microfluidic platform to model 3D cerebral microvessels (3D µvessels-on- chip) under controlled perfusion, enabling the study of endothelial differentiation and vascular organization. Human cerebral microvascular endothelial cells (HCMEC/D3) and induced pluripotent stem cell (iPSC)-derived endothelial cells are employed to evaluate vascular maturation under normoxia and hypoxia, the latter being a major driver of pathological angiogenesis in cancer and neurodegenerative disorders. This microfluidic model represents a physiologically relevant tool to dissect mechanisms of cerebral vasculogenesis/angiogenesis and to explore their role in health and disease. It also offers a versatile platform for translational applications, including the evaluation of therapeutic strategies targeting vascular dysfunction.

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