IMR Press / FBL / Volume 13 / Issue 17 / DOI: 10.2741/3178

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.

Disassembly of endothelial and epithelial junctions during leukocyte transmigration
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1 Department of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30322, USA

*Author to whom correspondence should be addressed.


Front. Biosci. (Landmark Ed) 2008, 13(17), 6638–6652;
Published: 1 May 2008

Leukocyte migration occurs as a response to inflammatory signals and is an efficient host defense mechanism against invading pathogens. This innate defense response includes transendothelial and transepithelial migration of leukocytes to facilitate clearance of inflammatory stimuli. The endothelium lines the vascular system and forms the first barrier for leukocytes as they migrate out of the bloodstream. The epithelium largely separates organs from the external environment and forms a second barrier for leukocytes. These cellular barriers are comprised of complex intercellular junctions of different molecular composition. However, for barrier function to be maintained, these specialized intercellular junctions must not be destroyed during transmigration. Innate immune cells including monocytes, neutrophils and dendritic cells are all capable of a highly regulated transmigration response in order to accomplish their different functions. These cells exploit many common adhesive and signaling cascades to traverse cellular junctions. However, there are unique features of each type of leukocyte and barrier that determine specificity of the response. This review will focus on highlighting the mechanisms that leukocytes exploit to open these junctions.

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