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PMID: 11490021 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Real-time imaging of vascular endothelial-cadherin during leukocyte transmigration across endothelium.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 167 ·No. 4 ·2001-08-15 ·Pages 2323-30

Shaw SK, Bamba PS, Perkins BN, Luscinskas FW

Abstract

Vascular endothelial-cadherin (VE-cadherin) is a component of the adherens junctions of endothelial cells whose role in endothelial transmigration of leukocytes has been controversial. Using a VE-cadherin/green fluorescent protein fusion construct (VEcadGFP) that mimics the native molecule, we visualized alterations in endothelial junctional structure in real time during transmigration of human neutrophils and monocytes in an in vitro flow model. We observed abundant transmigration occurring exclusively at the cell borders (paracellularly). Surprisingly, transmigration occurred both through de novo formation of transient gaps in VEcadGFP junctional distribution, and also through preexisting gaps. De novo gaps 4-6 microm in size were formed after a leukocyte arrived at a junction, whereas preexisting gaps were present even before the leukocyte had interacted with the endothelial cells contributing to a junction. Gaps rapidly resealed within 5 min after leukocyte transmigration. Migrating leukocytes appeared to push aside VEcadGFP in the plane of the junction, and this displaced material subsequently diffused back to refill the junction. To our knowledge, this is the first example where molecular events at the lateral junction have been tracked in real time during transmigration.

MeSH Terms
Antigens, CD Cadherins/biosynthesis,genetics,metabolism Cell Communication/genetics Cell Line Cell Membrane Permeability/genetics Cell Movement/genetics Cytoskeletal Proteins/metabolism Desmoplakins Diffusion Chambers, Culture/methods Endothelium, Vascular/cytology,metabolism,physiology Genetic Vectors/biosynthesis,physiology Green Fluorescent Proteins Hemorheology Humans Image Enhancement/instrumentation,methods Intercellular Junctions/metabolism Kinetics Leukocytes/cytology,metabolism,physiology Luminescent Proteins/biosynthesis,genetics,metabolism Microscopy, Fluorescence/instrumentation,methods Monocytes/cytology,metabolism,physiology Neutrophils/cytology,metabolism,physiology Trans-Activators Transfection beta Catenin
Chemicals
Antigens, CD CTNNB1 protein, human Cadherins Cytoskeletal Proteins Desmoplakins Luminescent Proteins Trans-Activators beta Catenin cadherin 5 Green Fluorescent Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Shaw S K
Vascular Research Division, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA. [email protected]
Bamba P S
Perkins B N
Luscinskas F W
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
2001-08-15
Pages
2323-30
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIDDK NIH HHS · DK02798 · United States
NHLBI NIH HHS · HL36028 · United States
NHLBI NIH HHS · HL53993 · United States
NHLBI NIH HHS · HL56985 · United States
NHLBI NIH HHS · HL65090 · United States
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