Abstract

Epithelial cells provide cell-cell adhesion that is essential to maintain the integrity of multicellular organisms. Epithelial cell-characterizing proteins, such as epithelial junctional proteins and transcription factors are well defined. However, the role of lipids in epithelial characterization remains poorly understood. Here we show that the phospholipid phosphatidylinositol (4,5)-bisphosphate [PI(4,5)P2] is enriched in the plasma membrane (PM) of epithelial cells. Epithelial cells lose their characteristics upon depletion of PM PI(4,5)P2, and synthesis of PI(4,5)P2 in the PM results in the development of epithelial-like morphology in osteosarcoma cells. PM localization of PARD3 is impaired by depletion of PM PI(4,5)P2 in epithelial cells, whereas expression of the PM-targeting exocyst-docking region of PARD3 induces osteosarcoma cells to show epithelial-like morphological changes, suggesting that PI(4,5)P2 regulates epithelial characteristics by recruiting PARD3 to the PM. These results indicate that a high level of PM PI(4,5)P2 plays a crucial role in the maintenance of epithelial characteristics.

Epithelial cells provide cell-cell adhesion to maintain the integrity of multicellular organisms. Here the authors show that phospholipid phosphatidylinositol (4,5)-bisphosphate is critical for the maintenance of epithelial characteristics.

Details

Title
Plasma membrane phosphatidylinositol (4,5)-bisphosphate is critical for determination of epithelial characteristics
Author
Kanemaru Kaori 1 ; Shimozawa Makoto 2   VIAFID ORCID Logo  ; Kitamata Manabu 2 ; Rikuto, Furuishi 1 ; Kayano Hinako 2 ; Sukawa Yui 2 ; Chiba Yuuki 2 ; Fukuyama Takatsugu 2 ; Hasegawa Junya 3 ; Nakanishi Hiroki 4 ; Kishimoto Takuma 5 ; Tsujita Kazuya 6   VIAFID ORCID Logo  ; Tanaka Kazuma 5 ; Itoh Toshiki 6 ; Sasaki Junko 3 ; Sasaki Takehiko 3   VIAFID ORCID Logo  ; Fukami Kiyoko 2   VIAFID ORCID Logo  ; Nakamura, Yoshikazu 1   VIAFID ORCID Logo 

 Tokyo University of Science, Department of Applied Biological Science, Faculty of Science and Technology, Noda, Japan (GRID:grid.143643.7) (ISNI:0000 0001 0660 6861) 
 Tokyo University of Pharmacy and Life Sciences, Laboratory of Genome and Biosignals, School of Life Sciences, Hachioji, Japan (GRID:grid.410785.f) (ISNI:0000 0001 0659 6325) 
 Tokyo Medical and Dental University, Department of Biochemical Pathophysiology, Medical Research Institute, Bunkyo-ku, Japan (GRID:grid.265073.5) (ISNI:0000 0001 1014 9130); Tokyo Medical and Dental University, Department of Lipid Biology, Graduate School of Medical and Dental Sciences, Bunkyo-ku, Japan (GRID:grid.265073.5) (ISNI:0000 0001 1014 9130) 
 Akita University, Research Center for Biosignal, Akita-city, Japan (GRID:grid.251924.9) (ISNI:0000 0001 0725 8504); Lipidome Lab Co., Ltd, Akita-city, Japan (GRID:grid.251924.9) 
 Hokkaido University Graduate School of Life Science, Division of Molecular Interaction, Institute for Genetic Medicine, Sapporo, Japan (GRID:grid.39158.36) (ISNI:0000 0001 2173 7691) 
 Kobe University, Biosignal Research Center, Kobe, Japan (GRID:grid.31432.37) (ISNI:0000 0001 1092 3077); Kobe University Graduate School of Medicine, Division of Membrane Biology, Department of Biochemistry and Molecular Biology, Kobe, Japan (GRID:grid.31432.37) (ISNI:0000 0001 1092 3077) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2661266239
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.