Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients
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Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients
Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients
解放军医学杂志(英文版)2006年第5期 页码:321-325
Affiliations:
1. Department of Dermatology Southwest Hospital
2. Third Military Medical University
3. Department of Pathology
4. Nanfang Hospital
5. Southern Medical University
6. ,Guangzhou,510515
Author bio:
Funds:
Supported by the National Natural Science Foundation of China (No. 30271199)
DOI:
中图分类号:R593.241
纸质出版:2006
Accepted:
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Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients[J]. 解放军医学杂志(英文版), 2006,(5):321-325.
[1]游弋,郝飞,邓永键.Expression of caspase-3 and TRAIL receptors in CD4~+ and CD8~+ T cells of SLE patients[J].Journal of Medical Colleges of PLA,2006(05):321-325.
Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients[J]. 解放军医学杂志(英文版), 2006,(5):321-325.DOI:
[1]游弋,郝飞,邓永键.Expression of caspase-3 and TRAIL receptors in CD4~+ and CD8~+ T cells of SLE patients[J].Journal of Medical Colleges of PLA,2006(05):321-325.DOI:
Expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients
摘要
Abstract
<正>Objective: To study the expression of caspase-3 and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptors in the CD4 + and CD8+ T cells of systemic lupus enythematosus (SLE) patients. Methods: RT-PCR was used to analyze the expression of caspase-3 and TRAIL receptors in CD4+ and CD8+ T cells of SLE patients and normal subjects. Results: The death domain-containing TRAIL-R1/R2 as well as "decoy" TRAIL-R3/R4 were co-expressed in majority of CD4+ and CD8+ T cells in both SLE patients and normal subjects. The CD8+ T cells from SLE patients showed significantly higher expression of caspase-3 and TRAIL-R2 than those from normal subjects
and the expression was correlated with the activity of the disease. Conclusion: The TRAIL-R2 signal pathway might contribute to the apoptosis of T cells in SLE.
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