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Differences in the reduction kinetics of incorporated spin labels in undifferentiated and differentiated mouse neuroblastoma cells.

Abstract
Significant differences in the rate of reduction of two spin labels, 5-doxylstearic acid and TEMPOL, in the undifferentiated and differentiated NB-15 mouse neuroblastoma cells were demonstrated by using electron paramagnetic resonance (EPR) spectroscopy. The half-time (T1/2) values for decay of the EPR signal of 5-doxylstearic acid in the undifferentiated and differentiated neuroblastoma cells were 70 min and 290 min, respectively. The T1/2 values of TEMPOL in the undifferentiated and differentiated cells were 18 min and 34 min, respectively. The cellular reductant was characterized as non-protein-bound sulfhydryl groups. A corresponding difference in the cellular non-protein-bound sulfhydryl content, 19.30 nmol/mg protein for the undifferentiated cells and 6.78 nmol/mg protein for the differentiated cells, was observed. Comparison of the reduction rates of TEMPOL, 5-doxylstearic acid and 16-doxylstearic acid in the undifferentiated NB-15 cells suggested that the permeation of non-protein-bound sulfhydryl compounds from the cytosol to membrane may be responsible for the reduction of the lipid-soluble stearic acid spin labels.
AuthorsK Y Chen, M G McLaughlin
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 845 Issue 2 Pg. 189-95 (May 30 1985) ISSN: 0006-3002 [Print] Netherlands
PMID2986718 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Cyclic N-Oxides
  • Spin Labels
  • Sulfhydryl Compounds
  • 5-doxylstearic acid
  • 16-nitroxystearic acid
  • tempol
Topics
  • Animals
  • Cell Differentiation
  • Cell Line
  • Cell Membrane (metabolism)
  • Cyclic N-Oxides (metabolism)
  • Electron Spin Resonance Spectroscopy
  • Half-Life
  • Kinetics
  • Mice
  • Neuroblastoma (metabolism, pathology)
  • Oxidation-Reduction
  • Spin Labels
  • Sulfhydryl Compounds (metabolism)

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