Mitochondrial DNA reduced by hypoxic conditions in three-dimensional (3D) spheroid cell cultures.

Tumour Biol

Laboratory of Cellular and Molecular Biochemistry, Department of Materials and Life Science, Seikei University, 3-3-1 Kichijoji Kitamachi, Musashino, Tokyo, 180-8633, Japan.

Published: December 2014

AI Article Synopsis

  • - The study highlights that three-dimensional (3D) cell cultures mimic key features of solid tumors, including oxygen scarcity or hypoxia.
  • - Researchers found that mitochondrial DNA (mtDNA) levels were significantly lower in 3D cultured cancer cells compared to traditional two-dimensional (2D) monolayer cultures, but no significant differences were observed in mitochondrial fusion and fission-related mRNA and protein expression.
  • - The findings suggest that while mtDNA levels drop in 3D settings, this doesn't appear to impact the dynamics of mitochondrial fusion and fission, indicating that more research is needed to understand the regulation of mtDNA in these environments.

Article Abstract

Three-dimensional (3D) cell culture reflects many of the important properties of solid tumors, such as the inadequate diffusion of oxygen that results in hypoxia. To understand the mitochondrial states in cancer, we performed comparisons of the levels of mitochondrial DNA (mtDNA), fusion- and fission-related mitochondrial messenger RNA (mRNA), and mitochondrial protein expression between monolayer (2D)- and 3D-cultured cancer cells. The mtDNA levels were observed to be significantly lower in the 3D cells compared with the monolayer cells. In contrast, the differences in expression of the mitochondrial fusion- and fission-related mRNAs and mitochondrial proteins between 2D- and 3D-cultured cancer cells were not significant, as shown by real-time PCR and immunoblot analysis. Therefore, although mtDNA levels decrease as a whole during 3D culture, this does not appear to affect the fusion and fission of individual mitochondria. Indeed, the factors regulating mitochondrial dynamics during 3D cell culture remain unclear. This study provides the basis for future, more detailed studies on the regulation of mtDNA.

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Source
http://dx.doi.org/10.1007/s13277-014-2593-6DOI Listing

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