Document Detail


Preferential adhesion of leukocytes near bifurcations is endothelium independent.
MedLine Citation:
PMID:  20624406     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Leukocyte-endothelial interactions play central roles in many pathological conditions. However, the in vivo mechanisms responsible for nonuniform spatial distribution of adhering leukocytes to endothelial cells in microvascular networks are not clear. We used a combination of in vitro and in vivo methodologies to explain of this complex phenomenon. A mouse cremaster muscle model was used to study the spatial distribution of leukocyte-endothelial cell interaction in vivo. A PDMS-based synthetic microvascular network (SMN) device was used to study interactions of functionalized microspheres using a receptor-ligand system in a (endothelial) cell-free environment for the in vitro studies. Our in vivo and in vitro findings indicate that both leukocytes in vivo and microspheres in vitro preferentially adhere near bifurcation (within 1-2 diameters from the bifurcation). This adhesion pattern was found to be independent of the diameter of the vessels. These findings support our hypothesis that the fluidic patterns near bifurcations/junctions, and not the presence or cellular aspects of the system (e.g. cell deformation, cell signaling, heterogeneous distribution of adhesion molecules), is the main controlling factor behind the preferential adhesion patterns of leukocytes near bifurcations.
Authors:
Nazanin Tousi; Bin Wang; Kapil Pant; Mohammad F Kiani; Balabhaskar Prabhakarpandian
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2010-07-21
Journal Detail:
Title:  Microvascular research     Volume:  80     ISSN:  1095-9319     ISO Abbreviation:  Microvasc. Res.     Publication Date:  2010 Dec 
Date Detail:
Created Date:  2010-11-15     Completed Date:  2011-02-25     Revised Date:  2011-12-21    
Medline Journal Info:
Nlm Unique ID:  0165035     Medline TA:  Microvasc Res     Country:  United States    
Other Details:
Languages:  eng     Pagination:  384-8     Citation Subset:  IM    
Copyright Information:
Copyright © 2010 Elsevier Inc. All rights reserved.
Affiliation:
Department of Mechanical Engineering, Temple University, Philadelphia, PA, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Avidin / metabolism
Biotin / metabolism
Cell Adhesion*
Endothelial Cells / physiology*
Hemorheology
Image Interpretation, Computer-Assisted
Leukocytes / physiology*
Male
Mice
Mice, Inbred C57BL
Microcirculation
Microfluidic Analytical Techniques
Microscopy, Fluorescence
Microvessels / cytology,  physiology*
Regional Blood Flow
Stress, Mechanical
Grant Support
ID/Acronym/Agency:
2R44HL076034-02/HL/NHLBI NIH HHS; R44 HL076034-02/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
1405-69-2/Avidin; 58-85-5/Biotin

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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