98%
921
2 minutes
20
Pericytes enveloping the endothelium play an important role in the physiology and pathology of microvessels, especially in vessel maturation and stabilization. However, our understanding of fundamental pericyte biology is limited by the lack of a robust in vitro model system that allows researchers to evaluate the interactions among multiple cell types in perfusable blood vessels. The present work describes a microfluidic platform that can be used to investigate interactions between pericytes and endothelial cells (ECs) during the sprouting, growth, and maturation steps of neovessel formation. A mixture of ECs and pericytes was attached to the side of a pre-patterned three dimensional fibrin matrix and allowed to sprout across the matrix. The effects of intact coverage and EC maturation by the pericytes on the perfused EC network were confirmed using a confocal microscope. Compared with EC monoculture conditions, EC-pericyte co-cultured vessels showed a significant reduction in diameter, increased numbers of junctions and branches and decreased permeability. In response to biochemical factors, ECs and pericytes in the platform showed the similar features with previous reports from in vivo experiments, thus reflect various pathophysiological conditions of in vivo microvessels. Taken together, these results support the physiological relevancy of our three-dimensional microfluidic culture system but also that the system can be used to screen drug effect on EC-pericyte biology.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512698 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0133880 | PLOS |
Adv Sci (Weinh)
August 2025
School of Biological and Chemical Sciences, College of Science and Engineering, University of Galway, University Road, Galway, H91 TK33, Ireland.
Cerebral organoids (COs) are multicellular, self-organized, in vitro, 3D brain-like tissues used for developmental biology, disease modelling, and drug screening. However, their lack of vascularity renders them less physiologically accurate. Vascularization of COs remains challenging due to the different requirements between COs and vascular cells, limited vascular network penetration within the organoid, and the absence of luminal perfusion.
View Article and Find Full Text PDFFront Cardiovasc Med
August 2025
Experimental Cardiovascular Medicine, University of Bristol, Bristol, United Kingdom.
Background: Endothelial cells (ECs) induce vascular smooth muscle cells (VSMCs) relaxation via nitric oxide (NO), prostacyclin (PGI₂) and hyperpolarizing factors. Recent whole-genomic, single-cell transcriptomic analysis of human vascular cells has revealed angiotypic heterogeneity. However, it remains unknown whether vasorelaxant mediators reiterate this pattern.
View Article and Find Full Text PDFCardiovasc Res
August 2025
Ottawa Hospital Research Institute, Sinclair Centre for Regenerative Medicine Program, Ottawa, ON, Canada.
Background: Pulmonary arterial hypertension (PAH) is a lethal pulmonary vascular disease characterized by arteriolar pruning and occlusive vascular remodeling leading to increased pulmonary vascular resistance and eventually right heart failure. While endothelial cell (EC) injury and apoptosis are known triggers for this disease, the mechanisms by which they lead to complex arterial remodeling remain obscure.
Aims: We employed multiplexed single-cell RNA sequencing at multiple timepoints during the onset and progression of disease in a model of severe PAH to identify mechanisms involved in the development of occlusive arterial lesions.
Methods Mol Biol
August 2025
Department of Translational Biomedicine and Neuroscience, University of Bari Medical School, Bari, Italy.
Pericytes are enigmatic cells that contribute significantly to central nervous system (CNS) homeostasis, blood-brain barrier (BBB) regulation, angiogenesis, and maintenance of neurovascular integrity. These versatile cells are associated with blood vessels, embedded within the vascular basal lamina (VBL), and closest to endothelial cells (ECs). Their multifaceted roles in CNS physiology, development, and pathology have been implicated in various neurological disorders, such as stroke, Alzheimer's disease, and multiple sclerosis.
View Article and Find Full Text PDFJ Cereb Blood Flow Metab
August 2025
Department of Neurology, Leiden University Medical Center, Leiden, the Netherlands.
Cerebral amyloid angiopathy (CAA) is a common age-related small vessel disease characterized by amyloid-beta (Aβ) accumulation in cortical and leptomeningeal blood vessel walls. Reduced Aβ clearance in the vasculature elevates the risk of CAA, while increasing evidence indicates that enhanced Aβ production in neurons also contributes. The impact of Aβ on the diverse cell types of the neurovascular unit (NVU)-including endothelial cells (ECs), pericytes, neurons, vascular smooth muscle cells (VSMCs), and astrocytes-remains unclear.
View Article and Find Full Text PDF