Microsphere-Based Nanoindentation for the Monitoring of Cellular Cortical Stiffness Regulated by MT1-MMP

Small. 2018 Oct;14(41):e1803000. doi: 10.1002/smll.201803000. Epub 2018 Sep 14.

Abstract

Biophysical properties are intimately connected to metastatic functions and aggressiveness in cancers. Especially, cellular stiffness is regarded as a biomarker for the understanding of metastatic potential and drug sensitivity. Here, protease-mediated changes of cortical stiffness are identified due to the deformation of cytoskeleton alignment at a cortex. For the past few decades, membrane type 1-matrix metalloproteinase (MT1-MMP) has been well known as a kernel protease enriched in podosomes during metastasis for extracellular matrix degradation. However, the biophysical significance of MT1-MMP expressing cancer cells is still unknown. Therefore, the nanomechanics of cancer cells is analyzed by a nanoindentation using a microsphere-attached cantilever of atomic force microscopy (AFM). In conclusion, the results suggest that MT1-MMP has contributed as a key regulator in cytoskeletal deformation related with cancer metastasis. Particularly, the AFM-based nanoindentation system for the monitoring of cortical nanomechanics will be crucial to understand molecular networks in cancers.

Keywords: MT1‐MMP; atomic force microscopy; cancer mechanobiology; cortical stiffness; nanoindentation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytoskeleton / chemistry
  • Matrix Metalloproteinase 14 / chemistry*
  • Microscopy, Atomic Force
  • Microspheres*

Substances

  • Matrix Metalloproteinase 14