Abstract:
:Microtubules (MTs) control cell shape and intracellular cargo transport. The role of MT turnover in the migration of slow-moving cells through endothelial barriers remains unclear. To irreversibly interfere with MT disassembly, we have used the MT-stabilizing agent zampanolide (ZMP) in Β16F10 melanoma as amodel of slow-moving cells. ZMP-treated B16 cells failed to follow chemotactic gradients across rigid confinements and could not generate stable sub-endothelial pseudopodia under endothelial monolayers. In vivo, ZMP-treated Β16 cells failed to extravasate though lung capillaries. In contrast to melanoma cells, the chemotaxis and transendothelial migration of ZMP-treated Tcells were largely conserved. This is afirst demonstration that MT disassembly is akey checkpoint in the directional migration of cancer cells but not of lymphocytes.
journal_name
Cell Adh Migrjournal_title
Cell adhesion & migrationauthors
Roncato F,Regev O,Yadav SK,Alon Rdoi
10.1080/19336918.2021.1934958keywords:
["Cytoskeleton","cancer","metastasis","motility","taxol"]subject
Has Abstractpub_date
2021-12-01 00:00:00pages
166-179issue
1eissn
1933-6918issn
1933-6926journal_volume
15pub_type
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