Document Detail


Transient regulation of transport by pericytes in venular microvessels via trapped microdomains.
MedLine Citation:
PMID:  18216252     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A phenomenon that has defied explanation for two decades is the time scale for transient reabsorption in the classic experiments of Michel and Phillips on individually perfused frog mesentery microvessels. One finds that transient reabsorption lasts <2 min before a new steady state of low filtration is established when the lumen pressure is abruptly dropped from a high to a low value. Our experiments in frog and rat venular microvessels under a variety of conditions revealed the same time trend for new steady states to be established as in Michel and Phillips' experiments. In contrast, one theoretically predicts herein that the time required for the tissue albumin concentration to increase to values for a new steady state to be achieved through reabsorption is in the order of several hours. In this paper we propose a new hypothesis and theoretical model for this rapid regulation, namely that pericytes covering the interendothelial cleft exits create small trapped microdomains outside the cleft exits which regulate this transient behavior. Our electron microscopy studies on rat mesenteric venular microvessels reveal an average pericyte coverage of approximately 85%. The theoretical model based on this ultrastructural study predicts an equilibration time on the order of 1 min when the lumen pressure is abruptly lowered. The basic concept of a trapped microdomain can also be extended to microdomains in the interstitial space surrounding skeletal muscle capillaries.
Authors:
X Zhang; R H Adamson; F E Curry; S Weinbaum
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2008-01-23
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  105     ISSN:  1091-6490     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  2008 Jan 
Date Detail:
Created Date:  2008-01-30     Completed Date:  2008-02-25     Revised Date:  2009-11-18    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1374-9     Citation Subset:  IM    
Affiliation:
The Leni and Peter W. May Department of Orthopaedics, Mount Sinai School of Medicine, New York, NY 10029, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Aorta
Endothelium, Vascular / metabolism*,  physiology,  ultrastructure
Male
Mesentery / blood supply,  metabolism*,  ultrastructure
Microcirculation / metabolism,  ultrastructure
Pericytes / metabolism*,  ultrastructure
Protein Structure, Tertiary / physiology
Protein Transport / physiology
Rana pipiens
Rana temporaria
Rats
Rats, Sprague-Dawley
Serum Albumin / chemistry*,  metabolism*,  physiology
Venules / metabolism*,  physiology,  ultrastructure
Grant Support
ID/Acronym/Agency:
AR41210/AR/NIAMS NIH HHS; AR48699/AR/NIAMS NIH HHS; HL44485/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Serum Albumin
Comments/Corrections

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