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1 Department of Human Physiology, University of California, Davis, CA 95616, USA2 Department of Biomedical Engineering, The City College of New York, New York, NY 10031, USA
We hypothesized that ultrafiltrate crossing the luminal endothelial glycocalyx through infrequent discontinuities (gaps) in the tight junction (TJ) strand of endothelial clefts reduces albumin diffusive flux from tissue into the protected region of the cleft on the luminal side of the TJ. Thus, the effective oncotic pressure difference (

) opposing filtration is greater than that measured between lumen and interstitial fluid. To test this we measured 

across rat mesenteric microvessels perfused with albumin (50 mg ml1) with and without interstitial albumin at the same concentration within a few micrometres of the endothelium as demonstrated by confocal microscopy. We found 

was near 70% of luminal oncotic pressure when the tissue concentration equalled that in the lumen. We determined size and frequency of TJ strand gaps in endothelial clefts using serial section electron microscopy. We found nine gaps in the reconstructed clefts having mean spacing of 3.59 µm and mean length of 315 nm. The mean depth of the TJ strand near gaps was 67 nm and the mean cleft path length from lumen to interstitium was 411 nm. With these parameters our three-dimensional hydrodynamic model confirmed that fluid velocity was high at gaps in the TJ strand so that even at relatively low hydraulic pressures the albumin concentration on the tissue side of the glycocalyx was significantly lower than in the interstitium. The results conform to the hypothesis that colloid osmotic forces opposing filtration across non-fenestrated continuous capillaries are developed across the endothelial glycocalyx and that the oncotic pressure of interstitial fluid does not directly determine fluid balance across microvascular endothelium.
(Received 19 November 2003;
accepted after revision 5 April 2004;
first published online 8 April 2004)
Corresponding author R. H. Adamson: Department of Human Physiology, University of California, Davis, CA 95616, USA. Email: rhadamson{at}ucdavis.edu
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