Extended ultrastructural characterization of chordoma cells: the link to new therapeutic options

PLoS One. 2014 Dec 5;9(12):e114251. doi: 10.1371/journal.pone.0114251. eCollection 2014.

Abstract

Chordomas are rare bone tumors, developed from the notochord and largely resistant to chemotherapy. A special feature of this tumor is the heterogeneity of its cells. By combining high pressure freezing (HPF) with electron tomography we were able to illustrate the connections within the cells, the cell-cell interface, and the mitochondria-associated endoplasmic reticulum membrane complex that appears to play a special role among the characteristics of chordoma. These lipid raft-like regions are responsible for lipid syntheses and for calcium signaling. Compared to other tumor cells, chordoma cells show a close connection of rough endoplasmic reticulum and mitochondria, which may influence the sphingolipid metabolism and calcium release. We quantified levels of ceramide and glycosylceramide species by the methyl tert-butyl ether extraction method and we assessed the intracellular calcium concentration with the ratiometric fluorescent dye Fura-2AM. Measurements of the changes in the intracellular calcium concentration revealed an increase in calcium due to the application of acetylcholine. With regard to lipid synthesis, glucosylceramide levels in the chordoma cell line were significantly higher than those in normal healthy cells. The accumulation of glycosylceramide in drug resistant cancer cells has been confirmed in many types of cancer and may also account for drug resistance in chordoma. This study aimed to provide a deep morphological description of chordoma cells, it demonstrated that HPF analysis is useful in elucidating detailed structural information. Furthermore we demonstrate how an accumulation of glycosylceramide in chordoma provides links to drug resistance and opens up the field for new research options.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Neoplasms / pathology
  • Bone Neoplasms / ultrastructure*
  • Cell Line, Tumor
  • Chordoma / pathology
  • Chordoma / ultrastructure*
  • Drug Resistance, Neoplasm / genetics
  • Endoplasmic Reticulum, Rough / metabolism
  • Endoplasmic Reticulum, Rough / pathology
  • Endoplasmic Reticulum, Rough / ultrastructure*
  • Humans
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitochondria / ultrastructure*
  • Notochord / metabolism
  • Notochord / pathology
  • Notochord / ultrastructure
  • Sphingolipids / metabolism

Substances

  • Sphingolipids

Grants and funding

Financial support from the Medical University of Graz is gratefully acknowledged. No commercial benefits of any kind have been or will be received from institutions related directly or indirectly to the subject of the manuscript. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.