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Evaluation of Caspase Activation to Assess Innate Immune Cell Death
Published on: January 20, 2023
Temporal relationships between ceramide production, caspase activation and mitochondrial dysfunction in cell lines
C Rodriguez-Lafrasse1, G Alphonse, P Broquet
1INSERM U189, Department of Biochemistry, Lyon-Sud Medical School, BP12, 69921 Oullins Cedex, France. rodriguez@lyon-sud.univ-lyon1.fr
Abstract:
To clarify the chronology of events leading to anti-Fas-induced apoptosis, and the mechanisms of resistance to this death effector, we compared the response kinetics of three tumour cell lines that display varying sensitivity to anti-Fas (based on levels of apoptosis), in terms of ceramide release, mitochondrial function and the caspase-activation pathway. In the highly sensitive Jurkat cell line, early caspase-8 activation, observed from 2 h after treatment, was chronologically associated with an acute depletion of glutathione and the cleavage of caspase-3 and poly-ADP ribosyl polymerase (PARP), followed by a progressive fall in the mitochondrial transmembrane potential (Delta(psi)m), between 4 and 48 h after treatment. Ceramide levels began to increase 2 h after the addition of anti-Fas (with no increase during the first hour), and increased continuously to 640% of control cells at 48 h. In the moderately sensitive SCC61 adherent cells, comparable results were observed, though with lower levels of ceramide and a delay in the response kinetics, with apoptotic cells becoming flotant. Finally, despite early cleavage of caspase-8 at 2 h, and a sustained level of activation until 48 h, no apoptotic response was observed in anti-Fas-resistant SQ20B cells. This was confirmed by a lack of ceramide generation and mitochondrial changes, and by the absence of any detectable cleavage of caspase-3 or PARP. Inhibition of caspase processing, and amplification of endogenous ceramide signalling by pharmacological agents, allowed us to establish the order of cellular events, locating ceramide release after caspase-8 activation and before caspase-3 activation, and demonstrating a direct involvement for ceramide release in mitochondrial dysfunction. Furthermore, these experiments provide strong arguments for the role of endogenous ceramide as a key executor of apoptosis, rather than as a consequence of membrane alterations.
Insights
This study reveals that ceramide release is a key executor of apoptosis, occurring after caspase-8 activation but before caspase-3 activation, and directly causing mitochondrial dysfunction in cancer cells.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Anti-Fas-induced apoptosis is a critical cell death pathway.
- Understanding resistance mechanisms to anti-Fas therapy is crucial for cancer treatment.
- The precise order of events and role of ceramide in this pathway require clarification.
Purpose of the Study:
- To elucidate the chronological sequence of events in anti-Fas-induced apoptosis.
- To investigate the mechanisms underlying resistance to anti-Fas-mediated cell death.
- To determine the role of ceramide release and mitochondrial dysfunction in apoptosis.
Main Methods:
- Comparative kinetic analysis of three tumor cell lines with varying anti-Fas sensitivity.
- Measurement of ceramide release, mitochondrial membrane potential, and caspase activation (caspase-3, caspase-8, PARP cleavage).
- Pharmacological manipulation of caspase processing and ceramide signaling.
Main Results:
- In sensitive cells, caspase-8 activation preceded ceramide release, which preceded caspase-3/PARP cleavage and mitochondrial dysfunction.
- Resistant cells showed caspase-8 activation but lacked ceramide generation, caspase-3/PARP cleavage, and mitochondrial changes.
- Ceramide release was confirmed to occur after caspase-8 activation and before caspase-3 activation, directly impacting mitochondrial function.
Conclusions:
- Endogenous ceramide acts as a key executor of apoptosis, not merely a consequence of membrane damage.
- The sequential activation of caspases and ceramide release is critical for initiating apoptosis.
- Understanding these molecular events may inform strategies to overcome resistance to anti-Fas therapy.
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