4.2 Article

Moderate substrate stiffness induces vascular smooth muscle cell differentiation through cellular morphological and tensional changes

Journal

BIO-MEDICAL MATERIALS AND ENGINEERING
Volume 31, Issue 3, Pages 157-167

Publisher

IOS PRESS
DOI: 10.3233/BME-201087

Keywords

Cell biomechanics; mechanobiology; substrate stiffness; smooth muscle cell differentiation; atomic force microscopy (AFM)

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [17H02077, 19K22944]
  2. Naito Foundation, Japan
  3. Takahashi Industrial and Economic Research Foundation, Japan
  4. AMED-CREST from the Japan Agency for Medical Research and Development (AMED) [JP19gm0810005, JP20gm0810005]
  5. Grants-in-Aid for Scientific Research [19K22944, 17H02077] Funding Source: KAKEN

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BACKGROUND: Vascular smooth muscle cells (VSMCs) are one of the main components of arterial walls and actively remodel the arterial walls in which they reside through biomechanical signals applied to themselves. Contractile or differentiated VSMCs have been observed in normal blood vessels. In pathological vascular conditions, they become dedifferentiated from contractile to non-contractile or synthetic cells, and a similar change is observed when VSMCs are placed in culture conditions. The mechanisms regulating VSMC differentiation remain unclear at this stage. OBJECTIVE: In this paper we investigated the effects of substrate stiffness on the morphology, intercellular tension, and differentiation of VSMCs. METHODS: Rat VSMCs were cultured on polyacrylamide (PA) gels, with elastic moduli of 15 kPa, 40 kPa, and 85 kPa, and PDMS substrate with elastic modulus of 1 MPa, and their morphology, intercellular tension, and contractile differentiation were assessed. RESULTS: Using fluorescence microscope image-based analysis and nano-indentation imaging with atomic force microscopy, we found that cell spreading and stiffening were induced by substrate stiffening in VSMCs. Interestingly, VSMCs on PA gel substrates with medium stiffness (40 kPa) showed significant elongation and shape polarization, and their a -SMA with F-actin cytoskeleton expression ratio was significantly higher than those of cells on other substrates. CONCLUSION: The results indicate an existing optimal substrate stiffness for promoting VSMC differentiation, and also indicate that cell shape polarization might be a key factor for VSMC differentiation.

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