Stimulation of sub-sonic vibration promotes the differentiation of adipose tissue-derived mesenchymal stem cells into neural cells

Life Sci. 2012 Sep 24;91(9-10):329-37. doi: 10.1016/j.lfs.2012.07.022. Epub 2012 Jul 31.

Abstract

Aims: Adipose tissue-derived stem cells (AT-MSCs) have been proposed as a new source for nervous tissue damage due to their capacity of neural differentiation potential including neurons, oligodendrocytes and astrocytes. Recently, many studies have demonstrated that sub-sonic vibration (SSV) is an effective cell differentiation method but there have been no studies on the effect of SSV about AT-MSC differentiation into neural-like cells in vitro. Therefore, we examined the effect of SSV on AT-MSCs to investigate the differentiation potential of neural-like cells.

Main methods: We assessed the changes in AT-MSCs by SSV during 4 days at 10, 20, 30 and 40 Hz (1.0 V). After stimulation, they were analyzed by RT-PCR, Western blot and immunohistological analysis using neural cell type-specific genes and antibodies. Further, to confirm the neural differentiation, we investigated adipogenic genes for RT-PCR analysis. For a mechanism study, we analyzed activation levels in time course of ERK phosphorylation after SSV.

Key findings: After 4-day SSV exposure, we observed morphological changes of AT-MSCs. Further, SSV induced gene/protein levels of neural markers while inhibiting adipogenesis and they were mainly upregulated at 30 Hz. In addition, phosphorylated ERK level was increased in a time-dependent manner upon 30 Hz SSV for 6h.

Significance: These results demonstrated that SSV affects AT-MSCs differentiation potential and 30 Hz SSV affected neural differentiation on AT-MSCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis / physiology
  • Adipose Tissue / cytology
  • Adipose Tissue / metabolism*
  • Cell Differentiation / physiology*
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • Mesenchymal Stem Cells / metabolism*
  • Neurons / metabolism*
  • Phosphorylation
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Up-Regulation / physiology
  • Vibration*

Substances

  • Extracellular Signal-Regulated MAP Kinases