Induction of apoptosis by recombinant soluble human TRAIL in Jurkat cells
Gen-Hong Yao1, Li-Jun Ling, Jian-Feng Luan
1Department of Transfusion, Jinling Hospital, Medical School, Nanjing University, Nanjing 210002, Jiangsu, China. ygh71@tom.com
Objective:
To investigate the therapeutic potential of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), a member of the TNF superfamily, and to analyze TRAIL-induced apoptosis in Jurkat cells.
Methods:
Expression of TRAIL receptors (DR4 and DR5) was detected by reverse transcriptase-polymerase chain reaction (RT-PCR). Cytotoxic effects were determined by colony formation assay and a cell counting kit. The effects of recombinant TRAIL on apoptosis of Jurkat cells were determined by DNA fragmentation (DNA ladder) and PI staining. Changes in mitochondrial membrane potential were detected with JC-1 fluorescence.
Results:
TRAIL inhibited the proliferation and induced internucleosomal DNA fragmentation (characteristic of apoptosis) and loss of mitochondrial membrane potential.
Conclusion:
Recombinant soluble TRAIL can be used as a therapy for cancer.
Insights
Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) shows therapeutic potential by inhibiting cancer cell proliferation. TRAIL effectively induces apoptosis, a programmed cell death pathway, in Jurkat cells.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a key mediator of apoptosis.
- TRAIL belongs to the TNF superfamily and plays a role in immune regulation and cell death.
- Understanding TRAIL's mechanism in cancer cells is crucial for therapeutic development.
Purpose of the Study:
- To investigate the therapeutic potential of TRAIL.
- To analyze TRAIL-induced apoptosis in Jurkat cells.
Main Methods:
- Reverse transcriptase-polymerase chain reaction (RT-PCR) to detect TRAIL receptors (DR4 and DR5).
- Colony formation assay and cell counting kit to assess cytotoxic effects.
- DNA fragmentation (DNA ladder), PI staining, and JC-1 fluorescence to evaluate apoptosis and mitochondrial membrane potential.
Main Results:
- TRAIL significantly inhibited proliferation of Jurkat cells.
- TRAIL induced internucleosomal DNA fragmentation, a hallmark of apoptosis.
- TRAIL treatment led to a loss of mitochondrial membrane potential.
Conclusions:
- Recombinant soluble TRAIL demonstrates therapeutic potential for cancer treatment.
- TRAIL effectively induces apoptosis in cancer cells, suggesting its viability as a therapeutic agent.
More Related Videos
14:27CRISPR-Cas9-based Genome Engineering to Generate Jurkat Reporter Models for HIV-1 Infection with Selected Proviral Integration Sites
Published on: November 14, 2018
09:20Rapid In Vitro Cytotoxicity Evaluation of Jurkat Expressing Chimeric Antigen Receptor using Fluorescent Imaging
Published on: October 27, 2023
Related Concept Videos
The Extrinsic Apoptotic Pathway
The Intrinsic Apoptotic Pathway
