Perturbation of Akt Signaling, Mitochondrial Potential, and ADP/ATP Ratio in Acidosis-Challenged Rat Cortical Astrocytes

King Chuen Wu, Ka Shun Cheng, Yu Wen Wang, Yuh Fung Chen, Kar Lok Wong, Tzu Hui Su, Paul Chan, Yuk Man Leung

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Cells switch to anaerobic glycolysis when there is a lack of oxygen during brain ischemia. Extracellular pH thus drops and such acidosis causes neuronal cell death. The fate of astrocytes, mechanical, and functional partners of neurons, in acidosis is less studied. In this report, we investigated the signaling in acidosis-challenged rat cortical astrocytes and whether these signals were related to mitochondrial dysfunction and cell death. Exposure to acidic pH (6.8, 6.0) caused Ca2+ release and influx, p38 MAPK activation, and Akt inhibition. Mitochondrial membrane potential was hyperpolarized after astrocytes were exposed to acidic pH as soon as 1h and lasted for 24h. Such mitochondrial hyperpolarization was prevented by SC79 (an Akt activator) but not by SB203580 (a p38 inhibitor) nor by cytosolic Ca2+ chelation by BAPTA, suggesting that only the perturbation in Akt signaling was causally related to mitochondrial hyperpolarization. SC79, SB203580, and BAPTA did not prevent acidic pH-induced cell death. Acidic pH suppressed ROS production, thus ruling out the role of ROS in cytotoxicity. Interestingly, pH 6.8 caused an increase in ADP/ATP ratio and apoptosis; pH 6.0 caused a further increase in ADP/ATP ratio and necrosis. Therefore, astrocyte cell death in acidosis did not result from mitochondrial potential collapse; in case of acidosis at pH 6.0, necrosis might partly result from mitochondrial hyperpolarization and subsequent suppressed ATP production.

Original languageEnglish
Pages (from-to)1108-1117
JournalJournal of Cellular Biochemistry
Volume118
Issue number5
DOIs
Publication statusPublished - May 1 2017

Fingerprint

Cell death
Acidosis
Astrocytes
Adenosine Diphosphate
Rats
Adenosine Triphosphate
Cell Death
p38 Mitogen-Activated Protein Kinases
Cytotoxicity
Chelation
Neurons
Brain
Necrosis
Chemical activation
Switches
Apoptosis
Oxygen
Membranes
Mitochondrial Membrane Potential
Glycolysis

Keywords

  • ACIDOSIS
  • AKT
  • ASTROCYTES
  • MITOCHONDRIA HYPERPOLARIZATION

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Perturbation of Akt Signaling, Mitochondrial Potential, and ADP/ATP Ratio in Acidosis-Challenged Rat Cortical Astrocytes. / Wu, King Chuen; Cheng, Ka Shun; Wang, Yu Wen; Chen, Yuh Fung; Wong, Kar Lok; Su, Tzu Hui; Chan, Paul; Leung, Yuk Man.

In: Journal of Cellular Biochemistry, Vol. 118, No. 5, 01.05.2017, p. 1108-1117.

Research output: Contribution to journalArticle

Wu, King Chuen ; Cheng, Ka Shun ; Wang, Yu Wen ; Chen, Yuh Fung ; Wong, Kar Lok ; Su, Tzu Hui ; Chan, Paul ; Leung, Yuk Man. / Perturbation of Akt Signaling, Mitochondrial Potential, and ADP/ATP Ratio in Acidosis-Challenged Rat Cortical Astrocytes. In: Journal of Cellular Biochemistry. 2017 ; Vol. 118, No. 5. pp. 1108-1117.
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