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Talin is required to increase stiffness of focal molecular complex in its early formation process
- Source :
- Biochemical and Biophysical Research Communications. 518:579-583
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- For cellular adaptation in mechanical environments, it is important to consider transmission of forces from the outside to the inside of cells via a focal molecular complex. The focal molecular complex, which consists of integrin, talin, vinculin and actin, is known to form in response to a force applied via the extra-cellular matrix (ECM). In the early formation process of the complex, the complex–actin connection is reinforced. These structural changes of the nascent complex result in an increase in its mechanical integrity and overall stiffness, possibly leading to the maturation of the nascent complex by enhancing force transmission. In this study, we hypothesized that the complex component talin is a crucial factor in increasing the stiffness of the nascent complex. To test the hypothesis, we used atomic force microscopy (AFM) to measure the stiffness of the nascent complex using a probe coated with fibronectin. Stiffness measurements were conducted for intact and talin knocked-down cells. Our results demonstrated that talin was required to increase the stiffness of the nascent complex, which could be caused by the reinforced connection between the complex and actin filaments mediated by talin.
- Subjects :
- Talin
0301 basic medicine
Integrins
animal structures
Mechanotransduction
Cellular adaptation
Integrin
Biophysics
macromolecular substances
Matrix (biology)
Mechanotransduction, Cellular
Biochemistry
Stiffness
Cell Line
Atomic force microscopy
Mice
03 medical and health sciences
0302 clinical medicine
medicine
Animals
Molecular Biology
Actin
Focal molecular complex
biology
Chemistry
Cell Biology
Vinculin
Actins
Biomechanical Phenomena
Extracellular Matrix
Fibronectins
Fibronectin
Actin Cytoskeleton
030104 developmental biology
Gene Knockdown Techniques
030220 oncology & carcinogenesis
biology.protein
medicine.symptom
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 518
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....8cf8f4817bef63641cefffd46b453082