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Spatiotemporal distribution of PTEN before directed cell migration in monolayers.
Lu, Quanzhi; Sasaki, Saori; Sera, Toshihiro; Kudo, Susumu.
Afiliación
  • Lu Q; Department of Mechanical Engineering, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka-Shi, Fukuoka, 819-0395, Japan.
  • Sasaki S; Department of Mechanical Engineering, Faculty of Engineering, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka-Shi, Fukuoka, 819-0395, Japan.
  • Sera T; Department of Medical and Robotic Engineering Design, Faculty of Advanced Engineering, Tokyo University of Science, 6-3-1 Niijuku, Katsushika-ku, Tokyo, 125-8585, Japan.
  • Kudo S; Department of Mechanical Engineering, Faculty of Engineering, Kyushu University, 744 Motooka, Nishi-Ku, Fukuoka-Shi, Fukuoka, 819-0395, Japan. kudo.susumu.237@m.kyushu-u.ac.jp.
Article en En | MEDLINE | ID: mdl-38926230
ABSTRACT
The intracellular distribution of phosphatase and tensin homolog (PTEN) is closely related to directed cell migration. In single cells, PTEN accumulates at the rear of the cell before and during directed migration; however, the spatiotemporal distribution of PTEN in confluent cell monolayers, particularly before directed migration, remains unclear. In this study, we wounded a cell in confluent fetal rat skin keratinocytes (FRSKs) and examined the dynamics of PTEN in the cells adjacent to the wounded cell. In contrast to single-cell migration, we found that PTEN translocated to the nucleus before the beginning of directed migration. This nuclear translocation of PTEN did not occur in disconnected cells, and it was also suppressed by importin-ß inhibitor and actin inhibitor. When the nuclear localization of PTEN was inhibited by an importin-ß inhibitor, cell elongation in the direction of migration was also significantly inhibited. Our results indicate that PTEN translocation is induced by the disruption of cell-cell adhesion and requires the involvement of importin-ß and actin cytoskeleton signaling. In addition, phosphatidylinositol 3,4,5-triphosphate (PIP3) may regulate PTEN distribution through its localized accumulation at the cell edge. Our findings suggest that the translocation of PTEN is crucial for directed cell migration and for responding to mechanical environmental changes in confluent cell monolayers.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: In Vitro Cell Dev Biol Anim Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: In Vitro Cell Dev Biol Anim Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Japón