AI Article Synopsis

  • The study investigates changes in intracellular amino acid pools during the differentiation of rat PC12 cells induced by nerve growth factor (NGF).
  • Differentiated PC12 cells displayed increased levels of excitatory neurotransmitters like glutamic acid and aspartic acid, while levels of urea and taurine decreased.
  • Adding substances like taurine and aspartic acid had negligible effects on the viability of PC12 cells in serum-free conditions, highlighting significant changes in amino acid composition during neuronal differentiation.

Article Abstract

Background/aim: Although rat PC12 cells are a well-established model to investigate neuronal differentiation, survival and function, the reports of differentiation-associated changes in the intracellular amino acid pools of neurotransmitters have been limited. In this study, possible changes in the intracellular amino acid pools were investigated during nerve growth factor (NGF)-induced differentiation of PC12 cells.

Materials And Methods: Rat PC12 cells were induced to differentiate into neuronal cells by 50 ng/ml NGF in serum-free Dulbecco's Modified Eagle's medium, followed by the addition of fresh NGF-containing medium at day 3, without medium change. Cell viability was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) method. Intracellular amino acids were extracted by 5%trichloroacetic acid and quantified by amino acid analyzer.

Results: Differentiated PC12 cells showed high concentrations of excitatory neurotransmitters (glutamic acid and aspartic acid) and glutamine (energy supply). In contrast, urea and taurine levels declined with the progression of neuronal differentiation. Exogenous addition of taurine, urea, and L- and D- aspartic acid showed little or no effect on supporting viability of PC12 cells cultured in serum-free medium.

Conclusion: The present study demonstrated dramatic changes in the composition of intracellular amino acids during neuronal differentiation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365737PMC
http://dx.doi.org/10.21873/invivo.11392DOI Listing

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