Nagoshi Yuuki, Yamamoto Gou, Irie Tarou, Tachikawa Tetsuhiko
Department of Oral Pathology and Diagnosis, Showa University School of Dentistry, 1-5-8 Hatanodai, Tokyo, 142-8555, Japan.
Med Mol Morphol. 2006 Sep;39(3):154-60. doi: 10.1007/s00795-006-0325-8.
Focal adhesion kinase (FAK), a protein tyrosine kinase, has recently been suggested to play a role in signal transduction through integrins. In fact, FAK is involved in cell proliferation and cell motility by performing signal transduction through integrins. FAK-related non-kinase (FRNK) has been found to be an inhibitor of FAK. As the expression level of FRNK in the cell is very low, the study of FRNK has been preferentially performed by gene overexpression, up to the present, and the role of constitutive FRNK in cells remains unclear. We hypothesized that FRNK is involved in the adhesion of cells to the extracellular matrix (ECM) and investigated the expression of FRNK by time kinetic analysis shortly after cell seeding. We found that FRNK expression was significantly increased in the cells during the early stage of cell adhesion to the ECM. These data indicated that FRNK plays an important role in cell adhesion during the very early stages of cell culture.
黏着斑激酶(FAK)是一种蛋白质酪氨酸激酶,最近有研究表明它在通过整合素进行的信号转导中发挥作用。事实上,FAK通过整合素进行信号转导,参与细胞增殖和细胞迁移。黏着斑激酶相关非激酶(FRNK)被发现是FAK的一种抑制剂。由于细胞中FRNK的表达水平非常低,迄今为止,对FRNK的研究主要通过基因过表达来进行,而组成型FRNK在细胞中的作用仍不清楚。我们推测FRNK参与细胞与细胞外基质(ECM)的黏附,并在细胞接种后不久通过时间动力学分析研究了FRNK的表达。我们发现,在细胞黏附到ECM的早期阶段,细胞中FRNK的表达显著增加。这些数据表明,FRNK在细胞培养的早期阶段对细胞黏附起着重要作用。