The kinesin KIF1C and microtubule plus ends regulate podosome dynamics in macrophages

• Published in: Molecular biology of the cell 2006-06, Vol.17 (6), p.2811-2823
• Main Authors: Kopp, Petra, Lammers, Reiner, Aepfelbacher, Martin, Woehlke, Günther, Rudel, Thomas, Machuy, Nikolaus, Steffen, Walter, Linder, Stefan
• Format: Article
• Language: English
• Subjects: Cell Differentiation; Cell Membrane Structures - physiology; Cell Membrane Structures - ultrastructure; Cells, Cultured; Cloning, Molecular; Escherichia coli; Humans; Kinesin - deficiency; Kinesin - genetics; Kinesin - physiology; Macrophages - cytology; Macrophages - physiology; Microinjections; Microtubules - physiology; Mutagenesis; Plasmids; Reverse Transcriptase Polymerase Chain Reaction; RNA, Small Interfering - genetics; Transfection
• ISSN: 1059-1524; 1939-4586; 1059-1524
• DOI: 10.1091/mbc.e05-11-1010

Microtubules are important for the turnover of podosomes, dynamic, actin-rich adhesions implicated in migration and invasion of monocytic cells. The molecular basis for this functional dependency, however, remained unclear. Here, we show that contact by microtubule plus ends critically influences the cellular fate of podosomes in primary human macrophages. In particular, we identify the kinesin KIF1C, a member of the Kinesin-3 family, as a plus-end-enriched motor that targets regions of podosome turnover. Expression of mutation constructs or small interfering RNA-/short hairpin RNA-based depletion of KIF1C resulted in decreased podosome dynamics and ultimately in podosome deficiency. Importantly, protein interaction studies showed that KIF1C binds to nonmuscle myosin IIA via its PTPD-binding domain, thus providing an interface between the actin and tubulin cytoskeletons, which may facilitate the subcellular targeting of podosomes by microtubules. This is the first report to implicate a kinesin in podosome regulation and also the first to describe a function for KIF1C in human cells.