Not all (cells) who wander are lost: Upstream migration as a pervasive mode of amoeboid cell motility.

Not all (cells) who wander are lost: Upstream migration as a pervasive mode of amoeboid cell motility.
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DOI:
10.3389/fcell.2023.1291201
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发表时间:
2023
影响因子:
5.5
通讯作者:
Guin, Subham
Guin, Subham
中科院分区:
生物学2区
文献类型:
--
作者:
Buffone Jr, Alexander;Hammer, Daniel A.;Kim, Sarah Hyun Ji;Anderson, Nicholas R.;Mochida, Ai;Lee, Dong-Hun;Guin, Subham

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Leukocytes possess the ability to migrate upstream—against the direction of flow—on surfaces of specific chemistry. Upstream migration was first characterized in vitro for T-cells on surfaces comprised of intracellular adhesion molecule-1 (ICAM-1). Upstream migration occurs when the integrin receptor αLβ2 (also known as lymphocyte function-associated antigen-1, or LFA-1) binds to ICAM-1. LFA-1/ICAM-1 interactions are ubiquitous and are widely found in leukocyte trafficking. Upstream migration would be employed after cells come to arrest on the apical surface of the endothelium and might confer an advantage for both trans-endothelial migration and tissue surveillance. It has now been shown that several other motile amoeboid cells which have the responsibility of trafficking from blood vessels into tissues, such as Marginal zone B cells, hematopoietic stem cells, and neutrophils (when macrophage-1 antigen, Mac-1, is blocked), can also migrate upstream on ICAM-1 surfaces. This review will summarize what is known about the basic mechanisms of upstream migration, which cells have displayed this phenomenon, and the possible role of upstream migration in physiology and tissue homeostasis.
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