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

  • Minhee Ku
  • , Hyun Joon Kim
  • , Su Yee Yau
  • , Nara Yoon
  • , Nam Hee Kim
  • , Jong In Yook
  • , Jin Suck Suh
  • , Dae Eun Kim
  • , Jaemoon Yang

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

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.

Original languageEnglish
Article number1803000
JournalSmall
Volume14
Issue number41
DOIs
StatePublished - 11 Oct 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • atomic force microscopy
  • cancer mechanobiology
  • cortical stiffness
  • MT1-MMP
  • nanoindentation

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