Dynamic and coordinated single-molecular interactions at TM4SF5-enriched microdomains guide invasive behaviors in 2- and 3-dimensional environments

• Published in: The FASEB journal Vol. 31; no. 4; p. 1461
• Main Authors: Kim, Hye-Jin, Kwon, Sojung, Nam, Seo Hee, Jung, Jae Woo, Kang, Minkyung, Ryu, Jihye, Kim, Ji Eon, Cheong, Jin-Gyu, Cho, Chang Yun, Kim, Somi, Song, Dae-Geun, Kim, Yong-Nyun, Kim, Tai Young, Jung, Min-Kyo, Lee, Kyung-Min, Pack, Chan-Gi, Lee, Jung Weon
• Format: Journal Article
• Language: English
• Published: United States 01.04.2017
• Subjects: Cell Line, Tumor; Cell Movement; Cholesterol - metabolism; Glycosylation; HEK293 Cells; Hepatocytes - metabolism; Hepatocytes - physiology; Hepatocytes - ultrastructure; Humans; Integrin alpha5 - metabolism; Lipoylation; Membrane Microdomains - metabolism; Membrane Microdomains - ultrastructure; Membrane Proteins - metabolism; Protein Binding; Protein Processing, Post-Translational; Receptor, Epidermal Growth Factor - metabolism; migration; 3D cell culture; membrane proteins; protein interaction affinity; FCCS
• ISSN: 1530-6860
• DOI: 10.1096/fj.201600944rr

Membrane proteins sense extracellular cues and transduce intracellular signaling to coordinate directionality and speed during cellular migration. They are often localized to specific regions, as with lipid rafts or tetraspanin-enriched microdomains; however, the dynamic interactions of tetraspanins with diverse receptors within tetraspanin-enriched microdomains on cellular surfaces remain largely unexplored. Here, we investigated effects of tetraspan(in) TM4SF5 (transmembrane 4 L6 family member 5)-enriched microdomains (T ERMs) on the directionality of cell migration. Physical association of TM4SF5 with epidermal growth factor receptor (EGFR) and integrin α5 was visualized by live fluorescence cross-correlation spectroscopy and higher-resolution microscopy at the leading edge of migratory cells, presumably forming TM4SF5-enriched microdomains. Whereas TM4SF5 and EGFR colocalized at the migrating leading region more than at the rear, TM4SF5 and integrin α5 colocalized evenly throughout cells. Cholesterol depletion and disruption in TM4SF5 post-translational modifications, including -glycosylation and palmitoylation, altered TM4SF5 interactions and cellular localization, which led to less cellular migration speed and directionality in 2- or 3-dimensional conditions. TM4SF5 controlled directional cell migration and invasion, and importantly, these TM4SF5 functions were dependent on cholesterol, TM4SF5 post-translational modifications, and EGFR and integrin α5 activity. Altogether, we showed that TM4SF5 dynamically interacted with EGFR and integrin α5 in migratory cells to control directionality and invasion.-Kim, H.-J., Kwon, S., Nam, S. H., Jung, J. W., Kang, M., Ryu, J., Kim, J. E., Cheong, J.-G., Cho, C. Y., Kim, S., Song, D.-G., Kim, Y.-N., Kim, T. Y., Jung, M.-K., Lee, K.-M., Pack, C.-G., Lee, J. W. Dynamic and coordinated single-molecular interactions at TM4SF5-enriched microdomains guide invasive behaviors in 2- and 3-dimensional environments.