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Identification of Intracellular Signaling Events Induced in Viable Cells by Interaction with Neighboring Cells Undergoing Apoptotic Cell Death
Published on: December 27, 2016
Differential regulation of AKT, MAPK and GSK3β during C2-ceramide-induced neuronal death
Gonzalo Arboleda1, Yolanda Cárdenas, Yeldy Rodríguez
1Grupo de Neurociencias, Facultad de Medicina, Universidad Nacional de Colombia, Bogotá, Colombia. gharboledab@unal.edu.co
Abstract:
Evidence has implicated apoptosis as a mechanism underlying cell demise in diverse neurodegenerative diseases including Parkinson's disease (PD). Endogenous toxins and other stress signals activate the sphingomyelin pathway increasing the levels of ceramide, an important regulator of cell death. In the present paper we have analysed the contribution of PI3K/AKT-GSK3β and MAPK (ERK and JNK) pathways to cell death in a catecholaminergic cell line following exposure to C(2)-ceramide. We also explored the potential neuroprotective action of insulin-like growth factor-1 (IGF-1) and neurotrophin-3 (NT3). We demonstrated that C(2)-ceramide-induced cell death is associated to an early decrease in phosphorylation (inhibition) of PI3K/AKT and ERK, followed by phosphorylation (activation) of JNK and de-phosphorylation (activation) of glycogen synthase kinase-3 beta (GSK3β). NT3 and IGF-1 increased survival at early time points, but only IGF-1 is capable to attenuate C(2)-ceramide-mediated neuronal death, and this neuroprotection is associated to strong and permanent activation of AKT and inhibition of GSK3β. In conclusion, C(2)-ceramide initiates a series of events including an early inactivation of PI3K/AKT and ERK pathways followed by activation of JNK and activation of GSK3β and neuronal death, changes that are counteracted by IGF-1.
Insights
Ceramide triggers neuronal death pathways in Parkinson's disease models. Insulin-like growth factor-1 (IGF-1) protects neurons by activating AKT and inhibiting GSK3β, counteracting ceramide-induced apoptosis.
Area of Science:
- Neuroscience
- Cell Biology
- Biochemistry
Background:
- Apoptosis contributes to neuronal death in neurodegenerative diseases like Parkinson's disease (PD).
- Ceramide, a sphingomyelin pathway regulator, plays a key role in stress-induced cell death.
- Understanding signaling pathways involved in ceramide-induced neurotoxicity is crucial for developing therapeutic strategies.
Purpose of the Study:
- To investigate the roles of PI3K/AKT-GSK3β and MAPK (ERK, JNK) pathways in C(2)-ceramide-induced cell death.
- To explore the neuroprotective potential of insulin-like growth factor-1 (IGF-1) and neurotrophin-3 (NT3) against ceramide toxicity.
Main Methods:
- Utilized a catecholaminergic cell line exposed to C(2)-ceramide.
- Analyzed the phosphorylation status of key signaling proteins including AKT, ERK, JNK, and GSK3β.
- Assessed the effects of IGF-1 and NT3 on cell survival and signaling pathway activation.
Main Results:
- C(2)-ceramide induced cell death associated with early PI3K/AKT and ERK inhibition, followed by JNK activation and GSK3β activation.
- Both NT3 and IGF-1 promoted survival at early stages.
- IGF-1 effectively attenuated C(2)-ceramide-mediated neuronal death, linked to sustained AKT activation and GSK3β inhibition.
Conclusions:
- C(2)-ceramide triggers neuronal death via inactivation of PI3K/AKT and ERK, and activation of JNK and GSK3β.
- IGF-1 demonstrates significant neuroprotective effects against ceramide toxicity by modulating these critical signaling pathways.
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