摘要
目的探讨IL-35对急性髓系白血病(Acute Myeloid Leukemia,AML)细胞增殖和凋亡的影响。方法选取3例成人初诊AML患者的骨髓标本,使用流式细胞术(Flow Cytometry,FCM)分选原始细胞,IL-35处理AML原始细胞以及NB4细胞,FCM检测细胞凋亡,CCK8检测细胞增殖。结果 (1)IL-35显著上调AML细胞株中IL-35R的表达,同时还明显促进AML细胞株的增殖,进一步研究发现,IL-35预刺激的AML细胞株能显著抵抗阿糖胞苷(Ara-C)诱导的凋亡;(2)IL-35显著上调AML细胞中IL-35R的表达,同时显著促进AML细胞的增殖,而凋亡实验也发现IL-35预刺激的AML细胞能显著抵抗Ara-C诱导的凋亡。结论抑制性细胞因子IL-35可通过直接促进AML细胞增殖和抑制AML细胞的凋亡来参与AML的发生发展。
Objective To investigate the effect of IL-35 on proliferation and apoptosis of AML cells. Methods Bone marrow specimens of 3 adult ND AML patients were enrolled into this study. Primary cells were sorted by FCM,AML original cell and NB4 cells were treated by IL-35. Apoptosis was detected by FCM,and cell proliferation was detected by CCK8. Results( 1) IL-35 significantly up-regulated the expression of IL-35 R in AML cell lines,and it also promoted the proliferation of AML cell lines. Further studies showed that AML cell lines pre-stimulated by IL-35 can significantly resist apoptosis induced by Ara-C.( 2) IL-35 significantly up-regulated the expression of IL-35 R in AML cells,and significantly promoted the proliferation of AML cells. Apoptosis experiments also showed that AML cells pre-stimulated by IL-35 could significantly resist apoptosis induced by Ara-C. Conclusion The inhibitory cytokine IL-35 can participate in the development of AML by directly promoting the proliferation of AML cells and inhibiting the apoptosis of AML cells.
作者
王佳
陶千山
翟志敏
WANG Jia TAO Qianshan ZHAI Zhimin(Department of Hematology, the Second Affiliated Hospital of Anhui Medical University, Hefei 230601 China)
出处
《锦州医科大学学报》
CAS
2017年第5期1-4,I0001,I0002,共6页
Journal of Jinzhou Medical University