Literature DB >> 28073834

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

Hye-Jin Kim1, Sojung Kwon1, Seo Hee Nam2, Jae Woo Jung2, Minkyung Kang1, Jihye Ryu1, Ji Eon Kim1, Jin-Gyu Cheong1, Chang Yun Cho1, Somi Kim1, Dae-Geun Song1, Yong-Nyun Kim3, Tai Young Kim1, Min-Kyo Jung4, Kyung-Min Lee1, Chan-Gi Pack4, Jung Weon Lee5,2.   

Abstract

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 (T5ERMs) 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 N-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. © FASEB.

Entities:  

Keywords:  3D cell culture; FCCS; membrane proteins; migration; protein interaction affinity

Mesh:

Substances:

Year:  2017        PMID: 28073834     DOI: 10.1096/fj.201600944RR

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  12 in total

1.  TM4SF5 promotes metastatic behavior of cells in 3D extracellular matrix gels by reducing dependency on environmental cues.

Authors:  Dae-Geun Song; Gyu-Ho Lee; Seo Hee Nam; Jin-Gyu Cheong; Doyoung Jeong; Seo-Jin Lee; Cheol-Ho Pan; Jae Woo Jung; Hye-Jin Kim; Jihye Ryu; Ji Eon Kim; Somi Kim; Chang Yun Cho; Min-Kyung Kang; Kyung-Min Lee; Jung Weon Lee
Journal:  Oncotarget       Date:  2017-05-07

Review 2.  TM4SF5-Mediated Roles in the Development of Fibrotic Phenotypes.

Authors:  Jihye Ryu; Jung Weon Lee
Journal:  Mediators Inflamm       Date:  2017-03-26       Impact factor: 4.711

3.  Assembly of protein complexes restricts diffusion of Wnt3a proteins.

Authors:  Ritsuko Takada; Yusuke Mii; Elena Krayukhina; Yuusuke Maruyama; Kazuhiro Mio; Yoshikazu Sasaki; Takao Shinkawa; Chan-Gi Pack; Yasushi Sako; Chikara Sato; Susumu Uchiyama; Shinji Takada
Journal:  Commun Biol       Date:  2018-10-10

4.  Global analysis of protein homomerization in Saccharomyces cerevisiae.

Authors:  Yeonsoo Kim; Jong Pil Jung; Chan-Gi Pack; Won-Ki Huh
Journal:  Genome Res       Date:  2018-12-19       Impact factor: 9.043

5.  TM4SF18 is aberrantly expressed in pancreatic cancer and regulates cell growth.

Authors:  Megha Singhal; Mahsa Khatibeghdami; Daniel R Principe; Georgina E Mancinelli; Kyle M Schachtschneider; Lawrence B Schook; Paul J Grippo; Sam R Grimaldo
Journal:  PLoS One       Date:  2019-03-21       Impact factor: 3.240

6.  TM4SF5-mediated liver malignancy involves NK cell exhaustion-like phenotypes.

Authors:  Hyunseung Sun; Eunmi Kim; Jihye Ryu; Hyejin Lee; Eun-Ae Shin; Minhyeong Lee; Haesong Lee; Jeong-Hoon Lee; Jung-Hwan Yoon; Dae-Geun Song; Semi Kim; Jung Weon Lee
Journal:  Cell Mol Life Sci       Date:  2021-12-18       Impact factor: 9.261

Review 7.  CD44 Glycosylation as a Therapeutic Target in Oncology.

Authors:  Chengcheng Liao; Qian Wang; Jiaxing An; Jie Chen; Xiaolan Li; Qian Long; Linlin Xiao; Xiaoyan Guan; Jianguo Liu
Journal:  Front Oncol       Date:  2022-07-21       Impact factor: 5.738

8.  Estrogen-related receptor gamma functions as a tumor suppressor in gastric cancer.

Authors:  Myoung-Hee Kang; Hyunji Choi; Masanobu Oshima; Jae-Ho Cheong; Seokho Kim; Jung Hoon Lee; Young Soo Park; Hueng-Sik Choi; Mi-Na Kweon; Chan-Gi Pack; Ju-Seog Lee; Gordon B Mills; Seung-Jae Myung; Yun-Yong Park
Journal:  Nat Commun       Date:  2018-05-15       Impact factor: 14.919

Review 9.  Amino acid transporters as tetraspanin TM4SF5 binding partners.

Authors:  Jae Woo Jung; Ji Eon Kim; Eunmi Kim; Jung Weon Lee
Journal:  Exp Mol Med       Date:  2020-01-20       Impact factor: 8.718

10.  N-terminus-independent activation of c-Src via binding to a tetraspan(in) TM4SF5 in hepatocellular carcinoma is abolished by the TM4SF5 C-terminal peptide application.

Authors:  Haeng Eun Song; Yoonji Lee; Eunmi Kim; Chang Yun Cho; Oisun Jung; Doohyung Lee; Eun Goo Lee; Seo Hee Nam; Minkyung Kang; Stephani Joy Y Macalino; Ji Eon Kim; Jae Woo Jung; Sung Won Kwon; Sun Choi; Jung Weon Lee
Journal:  Theranostics       Date:  2021-07-06       Impact factor: 11.556

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