The Journal of Experimental Medicine
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Published online September 10, 2007
doi:10.1084/jem.20062596
The Journal of Experimental Medicine, Vol. 204, No. 10, 2349-2362
The Rockefeller University Press, 0022-1007 $30.00
© 2007 Baluk et al.
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ARTICLE

Functionally specialized junctions between endothelial cells of lymphatic vessels

Peter Baluk1,2,3, Jonas Fuxe1,2,3, Hiroya Hashizume1,2,3, Talia Romano1,2,3, Erin Lashnits1,2,3, Stefan Butz4, Dietmar Vestweber4, Monica Corada5, Cinzia Molendini5, Elisabetta Dejana5,6,7, and Donald M. McDonald1,2,3

1 Cardiovascular Research Institute, 2 Comprehensive Cancer Center, and 3 Department of Anatomy, University of California, San Francisco, San Francisco, CA 94143
4 Max-Planck-Institute for Molecular Biomedicine and Institute of Cell Biology, University of Münster, 48149 Münster, Germany
5 FIRC Institute of Molecular Oncology Foundation, 20139 Milan, Italy
6 Department of Biomolecular Sciences and Biotechnology, Faculty of Sciences, University of Milan, 20133 Milan, Italy
7 Mario Negri Institute for Pharmacological Research, 20156 Milan, Italy

CORRESPONDENCE Donald M. McDonald: donald.mcdonald{at}ucsf.edu

Recirculation of fluid and cells through lymphatic vessels plays a key role in normal tissue homeostasis, inflammatory diseases, and cancer. Despite recent advances in understanding lymphatic function (Alitalo, K., T. Tammela, and T.V. Petrova. 2005. Nature. 438:946–953), the cellular features responsible for entry of fluid and cells into lymphatics are incompletely understood. We report the presence of novel junctions between endothelial cells of initial lymphatics at likely sites of fluid entry. Overlapping flaps at borders of oak leaf–shaped endothelial cells of initial lymphatics lacked junctions at the tip but were anchored on the sides by discontinuous button-like junctions (buttons) that differed from conventional, continuous, zipper-like junctions (zippers) in collecting lymphatics and blood vessels. However, both buttons and zippers were composed of vascular endothelial cadherin (VE-cadherin) and tight junction–associated proteins, including occludin, claudin-5, zonula occludens–1, junctional adhesion molecule–A, and endothelial cell–selective adhesion molecule. In C57BL/6 mice, VE-cadherin was required for maintenance of junctional integrity, but platelet/endothelial cell adhesion molecule–1 was not. Growing tips of lymphatic sprouts had zippers, not buttons, suggesting that buttons are specialized junctions rather than immature ones. Our findings suggest that fluid enters throughout initial lymphatics via openings between buttons, which open and close without disrupting junctional integrity, but most leukocytes enter the proximal half of initial lymphatics.


Abbreviations used: button, button-like junction; EM, electron microscopy; ESAM, endothelial cell–selective adhesion molecule; JAM-A, junctional adhesion molecule–A; LYVE-1, lymphatic vascular endothelial hyaluronan receptor–1; MHC II, MHC class II; PECAM-1, platelet/endothelial adhesion molecule–1; VE-cadherin, vascular endothelial cadherin; zipper, zipper-like junction; ZO-1, zonula occludens–1.

P. Baluk and J. Fuxe contributed equally to this work.


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