Studying Cellular Focal Adhesion Parameters with Imaging and MATLAB Analysis

被引:0
|
作者
Yu, Ling-Yea [1 ,2 ]
Tseng, Ting-Jeng [1 ]
Lin, Hsuan-Chao [3 ]
Hsu, Chi-Lin [1 ,2 ]
Lu, Ting-Xuan [1 ,4 ]
Lin, Yu-Chiao [1 ]
Tseng, Miranda [1 ]
Tsai, Feng-Chiao [1 ,2 ]
机构
[1] Natl Taiwan Univ, Coll Med, Dept Pharmacol, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Immunol, Taipei, Taiwan
[4] Virginia Commonwealth Univ, Dept Human & Mol Genet, Richmond, VA USA
来源
BIO-PROTOCOL | 2023年 / 13卷 / 21期
关键词
Focal adhesion (FA); Serine-threonine kinase 40 (STK40); Cell signaling; Mitogen-activated protein kinase (MAPK); Mean signal; Thresholding; Segmentation; FA selection;
D O I
10.21769/BioProtoc.4867
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:11
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