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Phosphoinositide 3-kinase inhibitors protect mouse kidney cells from cyclosporine-induced cell death
E Sarró1, O Tornavaca, M Plana
1Departament de Bioquímica i Biologia Molecular, Unitat de Bioquímica de Biociències, Universitat Autònoma de Barcelona, Campus de Bellaterra, Barcelona 08193, Spain.
Abstract:
The use of cyclosporine has been restricted by its nephrotoxic effects mediated, in part, by reactive oxygen species (ROS). Phosphoinositide 3-kinase, protein kinase B, and extracellular regulated kinase (ERK) pathways are related to survival and cell death and are activated after ROS generation. In this study, we evaluated the effects of cyclosporine on these pathways and their contribution to cyclosporine-induced toxicity. Viability of cells derived from the proximal tubule of transgenic mice was measured with Trypan Blue, ROS generation by a fluorescent probe, while ERK and phosphoinositide 3-kinase/protein kinase B activation were monitored with phospho-specific antibodies. Cyclosporine decreased cell viability and induced ROS generation and ERK and phosphoinositide 3-kinase activation. Both pathways were activated by the epidermal growth factor receptor (EGFR). Antioxidants blocked ERK activation but failed to inhibit protein kinase B phosphorylation or prevent cyclosporine toxicity. ERK inhibition did not protect from cyclosporine-induced cell death. EGFR or phosphoinositide 3-kinase inhibitors protected from cyclosporine-triggered cell death without decreasing ROS. Small interfering RNA against the catalytic subunit of phosphoinositide 3-kinase decreased protein kinase B phosphorylation but did not prevent cyclosporine-mediated cell death. Our results show that EGFR mediates the cytotoxic effects of cyclosporine through an ROS-independent mechanism. Cyclosporine-induced cell death is triggered by a non-classical phosphoinositide 3-kinase and does not require ERK activation.
Insights
Cyclosporine causes kidney toxicity partly via reactive oxygen species (ROS). This study reveals epidermal growth factor receptor (EGFR) mediates cyclosporine
Area of Science:
- Nephrology
- Cell Biology
- Molecular Pharmacology
Background:
- Cyclosporine (CsA) is a vital immunosuppressant with dose-limiting nephrotoxicity.
- Reactive oxygen species (ROS) and signaling pathways like phosphoinositide 3-kinase (PI3K)/protein kinase B (Akt) and extracellular signal-regulated kinase (ERK) are implicated in CsA toxicity.
Purpose of the Study:
- To investigate the role of PI3K/Akt and ERK pathways in CsA-induced kidney cell toxicity.
- To determine the involvement of epidermal growth factor receptor (EGFR) in mediating CsA effects.
Main Methods:
- Primary mouse proximal tubule cells were used.
- Cell viability was assessed using Trypan Blue exclusion.
- ROS generation was measured via fluorescent probes.
- Pathway activation (PI3K/Akt, ERK) was monitored using phospho-specific antibodies.
- Inhibitors and small interfering RNA (siRNA) were employed to probe pathway function.
Main Results:
- Cyclosporine reduced cell viability, increased ROS, and activated PI3K/Akt and ERK pathways, with EGFR involvement.
- Antioxidants blocked ERK but not Akt activation or toxicity.
- ERK inhibition did not prevent cell death.
- EGFR or PI3K inhibition protected cells from CsA toxicity independently of ROS reduction.
- siRNA targeting PI3K catalytic subunit reduced Akt phosphorylation but not CsA-induced cell death.
Conclusions:
- EGFR mediates cyclosporine's cytotoxic effects through an ROS-independent mechanism.
- Cyclosporine-induced cell death involves a non-canonical PI3K pathway and does not require ERK activation.
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