Literature DB >> 17713348

Frequency-dependent phenotype modulation of vascular smooth muscle cells under cyclic mechanical strain.

Ming-Juan Qu1, Bo Liu, Han-Qin Wang, Zhi-Qiang Yan, Bao-Rong Shen, Zong-Lai Jiang.   

Abstract

Phenotype transformation of vascular smooth muscle cells (VSMCs) is known to be modulated by mechanical strain. The present study was designed to investigate how different frequencies of mechanical strain affected VSMC phenotype. VSMCs were subjected to the strains of 10% elongation at 0, 0.5, 1 and 2 Hz for 24 h using a Flexercell strain unit. VSMC phenotype was assessed by cell morphology, measurement of two-dimensional cell area, Western blotting for protein and RT-PCR for mRNA expression of differentiation markers. Possible protein kinases involved were evaluated by Western blotting with their specific antibodies. The strains at certain frequencies could induce a contractile morphology in VSMC with almost perpendicular alignment to the strain direction. The strains also regulated protein and mRNA expression of several differentiation markers, as well as the activation of extracellular signal-regulated kinases (ERKs), p38 MAP kinase and protein kinase B (Akt) in a frequency-dependent manner. Furthermore, the inhibition of the p38 pathway could block the frequency-induced phenotype modulation of VSMCs, but not inhibition of ERK or Akt pathways. These results indicate that the frequency of cyclic strain can result in the differentiated phenotype of VSMCs, and it is mediated at least partly by the activation of the p38 pathway. Copyright 2007 S. Karger AG, Basel.

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Year:  2007        PMID: 17713348     DOI: 10.1159/000102278

Source DB:  PubMed          Journal:  J Vasc Res        ISSN: 1018-1172            Impact factor:   1.934


  18 in total

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3.  Role of cyclic strain frequency in regulating the alignment of vascular smooth muscle cells in vitro.

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Review 7.  Computational Fluid Dynamics and Additive Manufacturing to Diagnose and Treat Cardiovascular Disease.

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8.  Stretch-induced stress fiber remodeling and the activations of JNK and ERK depend on mechanical strain rate, but not FAK.

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9.  TRPV4 channels mediate cyclic strain-induced endothelial cell reorientation through integrin-to-integrin signaling.

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10.  Cell-shape regulation of smooth muscle cell proliferation.

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