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Studying Cellular Focal Adhesion Parameters with Imaging and MATLAB Analysis.
Yu, Ling-Yea; Tseng, Ting-Jeng; Lin, Hsuan-Chao; Hsu, Chi-Lin; Lu, Ting-Xuan; Lin, Yu-Chiao; Tseng, Miranda; Tsai, Feng-Chiao.
Afiliação
  • Yu LY; Department of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Tseng TJ; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Lin HC; Department of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Hsu CL; Department of Immunology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Lu TX; Department of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Lin YC; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
  • Tseng M; Department of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
  • Tsai FC; Department of Pharmacology, National Taiwan University College of Medicine, Taipei, Taiwan.
Bio Protoc ; 13(21): e4867, 2023 Nov 05.
Article em En | MEDLINE | ID: mdl-37969758
Cell signaling is highly integrated for the process of various cell activities. Although previous studies have shown how individual genes contribute to cell migration, it remains unclear how the integration of these signaling pathways is involved in the modulation of cell migration. In our two-hit migration screen, we revealed that serine-threonine kinase 40 (STK40) and mitogen-activated protein kinase (MAPK) worked synergistically, and the suppression of both genes could further lead to suppression in cell migration. Furthermore, based on our analysis of cellular focal adhesion (FA) parameters using MATLAB analysis, we are able to find out the synergistic reduction of STK40 and MAPK that further abolished the increased FA by shSTK40. While FA identification in previous studies includes image analysis using manual selection, our protocol provides a semi-automatic manual selection of FAs using MATLAB. Here, we provide a method that can shorten the amount of time required for manual identification of FAs and increase the precision for discerning individual FAs for various analyses, such as FA numbers, area, and mean signals.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Bio Protoc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Bio Protoc Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Estados Unidos