On the Value of In Vitro Cell Systems for Mechanobiology from the Perspective of Yes-Associated Protein/Transcriptional Co-Activator with a PDZ-Binding Motif and Focal Adhesion Kinase and Their Involvement in Wound Healing, Cancer, Aging, and Senescence.
Thorsten SteinbergMartin Philipp DieterleImke RammingerCharlotte KleinJulie BrossetteAyman HusariPascal TomakidiPublished in: International journal of molecular sciences (2023)
Mechanobiology comprises how cells perceive different mechanical stimuli and integrate them into a process called mechanotransduction; therefore, the related mechanosignaling cascades are generally important for biomedical research. The ongoing discovery of key molecules and the subsequent elucidation of their roles in mechanobiology are fundamental to understanding cell responses and tissue conditions, such as homeostasis, aging, senescence, wound healing, and cancer. Regarding the available literature on these topics, it becomes abundantly clear that in vitro cell systems from different species and tissues have been and are extremely valuable tools for enabling the discovery and functional elucidation of key mechanobiological players. Therefore, this review aims to discuss the significant contributions of in vitro cell systems to the identification and characterization of three such key players using the selected examples of yes-associated protein (YAP), its paralog transcriptional co-activator with a PDZ-binding motif (TAZ), and focal adhesion kinase (FAK) and their involvement in wound healing, cancer, aging, and senescence. In addition, the reader is given suggestions as to which future prospects emerge from the in vitro studies discussed herein and which research questions still remain open.
Keyphrases
- wound healing
- single cell
- papillary thyroid
- cell therapy
- gene expression
- dna damage
- endothelial cells
- squamous cell
- systematic review
- small molecule
- squamous cell carcinoma
- high throughput
- tyrosine kinase
- cell death
- cystic fibrosis
- staphylococcus aureus
- current status
- protein kinase
- cell cycle arrest
- heat shock
- cell proliferation
- candida albicans