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Extracellular ATP activates different signalling pathways in rat Sertoli cells
The Biochemical Journal
|October 1, 1995
Summary
Extracellular ATP (ATPe) triggers sodium influx and plasma membrane depolarization in rat Sertoli cells. It also causes calcium release and influx via voltage-operated calcium channels, involving G-protein signaling.
Area of Science:
- Cell Biology
- Neuroscience
- Endocrinology
Background:
- Sertoli cells play a crucial role in male reproduction.
- Extracellular ATP (ATPe) is a signaling molecule with diverse cellular effects.
- Understanding ATPe's impact on Sertoli cell function is vital for reproductive health research.
Purpose of the Study:
- To investigate the effects of extracellular ATP (ATPe) on plasma membrane potential and intracellular calcium concentrations ([Ca2+]i) in rat Sertoli cells.
- To elucidate the signaling pathways involved in ATPe-mediated cellular responses.
Main Methods:
- Rat Sertoli cells were stimulated with ATPe and other nucleotides.
- Plasma membrane potential and [Ca2+]i were monitored using fluorescent dyes (bis-oxonol and fura-2/AM).
- Ionic changes were analyzed under various conditions, including altered extracellular ion concentrations and treatment with specific inhibitors (thapsigargin, verapamil, nifedipine, pertussis toxin).
Main Results:
- ATPe induced rapid plasma membrane depolarization dependent on extracellular Na+ influx.
- ATPe caused a biphasic increase in [Ca2+]i: an initial spike from intracellular stores and a sustained phase dependent on Ca2+ influx via voltage-operated calcium channels (VOCCs).
- Pertussis toxin partially reduced ATPe-induced responses, indicating involvement of pertussis toxin-sensitive G-proteins.
Conclusions:
- Rat Sertoli cells possess P2-purinergic receptors activated by ATPe.
- ATPe triggers distinct signaling pathways: Na+ influx causing depolarization and Ca2+ release/influx.
- These findings reveal complex ATPe-mediated signaling in Sertoli cells, potentially impacting reproductive function.