Capillary bed 2026-11-05
A capillary bed is a network of capillaries connecting arterioles to venules. It spreads blood flow across many small vessels, providing a large exchange surface between blood plasma and surrounding interstitial fluid. Upstream vascular resistance and the arrangement of the network affect how much blood reaches that surface.[ref]
Anatomy and Physiology 2e by J. Gordon Betts and others. §20.2, blood flow, blood pressure and resistance
The aggregate cross-sectional area helps explain why narrow individual vessels need not imply rapid transit. In an ideal model with identical open capillaries of radius sharing total volumetric flow rate equally, the mean axial velocity isAt fixed and , doubling halves . This is a conservation of mass calculation; actual exchange also depends on the wall, the exchanged substance and uneven flow through real networks.
The endothelial glycocalyx is one such wall feature. R. H. Adamson and colleagues found that effective oncotic pressure still opposed filtration when bulk albumin concentrations on both sides of rat microvessels were matched. Their imaging and modelling implicated the local environment near the endothelial glycocalyx, showing why bulk interstitial fluid measurements alone do not specify the filtration barrier.[ref]
Mia Phillipson 2026-11-05
Mia Phillipson is a researcher in physiology and inflammation. In a 2006 collaborative study, Mia Phillipson and colleagues used intravital microscopy to follow neutrophils inside inflamed mouse venules. The movies showed that after cell adhesion to the endothelium, neutrophils often crawled along the inner surface before leaving the blood vessel.[ref]
Intraluminal crawling of neutrophils to emigration sites: a molecularly distinct process from adhesion in the recruitment cascade by Mia Phillipson and others. Abstract and Results: real-time and time-lapse microscopy; Journal of Experimental Medicine 203, 2569–2575, 2006
The team compared mice lacking different integrins, the adhesion-related proteins LFA-1 and Mac-1. Loss of LFA-1 strongly reduced initial cell adhesion. Loss of Mac-1 allowed cell adhesion but severely reduced subsequent crawling and delayed passage out of the blood vessel. Watching successive steps revealed distinct functions that a single count of attached neutrophils would have missed. The experiment therefore separates arrival, crawling and exit as experimentally distinguishable stages of the inflammatory response.[ref]
Intraluminal crawling of neutrophils to emigration sites: a molecularly distinct process from adhesion in the recruitment cascade by Mia Phillipson and others. Abstract: contrasting LFA-1 and Mac-1 knockout phenotypes and delayed transmigration
Postcapillary venule 2026-11-05
A postcapillary venule is a small venule immediately downstream of a capillary network. Its thin wall includes an endothelium supported by associated pericytes. It collects blood returning from exchange vessels and is an important site of leukocyte passage from the circulation into surrounding tissue.[ref]
Anatomy and Physiology 2e by J. Gordon Betts and others. Section20.1, Venules and vessel-wall organization
In a 2006 experiment, investigators followed neutrophils in inflamed mouse postcapillary venules using real-time and time-lapse intravital microscopy. After adhering, the neutrophils crawled along the luminal surface before leaving the vessel, sometimes moving against blood flow. Genetic perturbations separated effective adhesion from subsequent crawling.[ref]
Venule 2026-11-05
A venule is a small blood vessel that collects blood leaving capillaries and conveys it toward larger veins. It lies on the returning side of the microcirculation: arterioles supply the capillary network, while venules drain it. The smallest postcapillary venules have thin walls lined by endothelium.[ref]
A venule is also an important interface between flowing blood and surrounding tissue. In an experiment using time-lapse intravital microscopy, investigators followed neutrophils within inflamed mouse postcapillary venules. After adhering, the neutrophils crawled along the inner surface toward sites where they could leave the vessel. Observing movement over time distinguished this searching step from the initial arrest.[ref]
Intraluminal crawling of neutrophils to emigration sites: a molecularly distinct process from adhesion in the recruitment cascade by Mia Phillipson and others. Abstract and Results: intraluminal crawling after adhesion