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pmid: 11577244
Evidence from a variety of sources suggests that pericytes have contractile properties and may therefore function in the regulation of capillary blood flow. However, it has been suggested that contractility is not a ubiquitous function of pericytes, and that pericytes surrounding true capillaries apparently lack the machinery for contraction. The present study used a variety of techniques to investigate the expression of contractile proteins in the pericytes of the CNS. The results of immunocytochemistry on cryosections of brain and retina, retinal whole-mounts and immunoblotting of isolated brain capillaries indicate strong expression of the smooth muscle isoform of actin (alpha-SM actin) in a significant number of mid-capillary pericytes. Immunogold labelling at the ultrastructural level showed that alpha-SM actin expression in capillaries was exclusive to pericytes, and endothelial cells were negative. Compared to alpha-SM actin, non-muscle myosin was present in lower concentrations. By contrast, smooth muscle myosin isoforms, were absent. Pericytes were strongly positive for the intermediate filament protein vimentin, but lacked desmin which was consistently found in vascular smooth muscle cells. These results add support for a contractile role in pericytes of the CNS microvasculature, similar to that of vascular smooth muscle cells.
Male, Microcirculation, Calcium-Binding Proteins, Microfilament Proteins, Retinal Vessels, Smooth Muscle Myosins, Actins, Desmin, Rats, Immunoenzyme Techniques, Platelet Endothelial Cell Adhesion Molecule-1, Rats, Sprague-Dawley, Contractile Proteins, Blood-Brain Barrier, Animals, Vimentin, Calponins, Microscopy, Immunoelectron, Pericytes, Cytoskeleton
Male, Microcirculation, Calcium-Binding Proteins, Microfilament Proteins, Retinal Vessels, Smooth Muscle Myosins, Actins, Desmin, Rats, Immunoenzyme Techniques, Platelet Endothelial Cell Adhesion Molecule-1, Rats, Sprague-Dawley, Contractile Proteins, Blood-Brain Barrier, Animals, Vimentin, Calponins, Microscopy, Immunoelectron, Pericytes, Cytoskeleton
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 214 | |
popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |