Abnormal expression of histone acetylases in CD8+T cells of patients with severe aplastic anemia

被引:4
作者
Qi, Weiwei [1 ]
Zhang, Yu [1 ]
Wang, Yachen [1 ]
Wang, Huaquan [1 ]
Fu, Rong [1 ]
Shao, Zonghong [1 ]
机构
[1] Tianjin Med Univ, Dept Hematol, Gen Hosp, 154 Anshan St, Tianjin 300052, Peoples R China
基金
中国国家自然科学基金;
关键词
CD8+T cells; HATs; HDACs; IFN-gamma; severe aplastic anemia; T-CELLS;
D O I
10.1002/jcla.24339
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Introduction: We aimed to investigate the balance between the mRNA levels of histone acetyltransferases (HATs) and histone deacetylases (HDACs) in CD8+ T cells of patients with severe aplastic anemia (SAA). Methods: Twenty untreated SAA patients, 18 remission SAA patients (R-SAA), and 22 normal controls were evaluated. The mRNA expression levels of HATs, HDACs, and IFNG in CD8+ T cells were measured by real-time quantitative reverse transcription polymerase chain reaction. Results: Histone acetylase EP300 and CREBBP mRNA levels were significantly elevated in CD8+ T cells of SAA patients compared with the normal controls (both p < 0.05). No significant differences were observed in HDAC1 and HDAC7 mRNA between SAA patients and the normal controls. There was an obvious positive correlation between IFNG and EP300 (r = 0.5126, p < 0.01), and CREBBP (r = 0.4663, p < 0.05), respectively, in SAA and R-SAA patients. In addition, EP300 and CREBBP mRNA levels were clearly correlated with clinical parameters of peripheral blood and bone marrow in those patients. Conclusion: Our findings suggest that EP300 and CREBBP are increased in CD8+ T cells of SAA patients and are correlated with disease severity. The imbalances in HATs and HDACs may play a role in activating CD8+ T cells to promote the immune pathogenesis of SAA.
引用
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页数:8
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