Bian Yu-Jie, Li Wei-Wang, Li Meng-Ke, Wang Bi-Chen, Shi De-Yang, Shi Jun, Yuan Wei-Ping, Chu Ya-Jing
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.
State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2021 Apr;29(2):557-566. doi: 10.19746/j.cnki.issn.1009-2137.2021.02.040.
AbstractObjective: To establish an acquired aplastic anemia animal model for investigating the function of T lymphocyte and the pathogenesis and treatment of aplastic anemia(AA).
To establish the acquired aplastic anemia mouse model through the X-ray irradiation in combination with lymphocytes injection. AA Group: the purified Pan T lymphocytes from the spleen of C57BL/6J mice were enriched and injected to the mice through tail vein(5×10), the CB6F1 mice were exposed to 3,4 and 5 Gy X-ray irradiation; TBI Group: the CB6F1 mice were exposed to 3,4 and 5 Gy X-ray irradiation, and were injected with the same volume of PBS buffer; Control group: the CB6F1 mice were only injected with the same volume of PBS buffer. The peripheral blood routine was examined and the number of nucleated cells in bone marrow were calculated;the hematopoiesis changes in bone marrow was examined;flow cytometry was used to examine the distribution of T lymphocytes in bone marrow, and it also used to examine the apoptosis of bone marrow cells and the differentiation of spleen T lymphocytes.
Compared with 4, 5 Gy irradiated mice in AA groups, the survival time of 3 Gy irradiated AA groups was significantly prolonged. 3, 4 and 5 Gy X-ray irradiation combined with Pan T lymphocyte injection could successfully induced severe reduction of red blood cells, blood neutrophils, and platelets, severe reduction of bone marrow nucleated cells, severe bone marrow hematopoietic failure, and the significant expansion of T lymphocytes ratio in the bone marrow. CD4 and CD8 T cells were both increased, but mainly on CD8 T cells, and could promote the differentiation of T cells from naïve T cells to effector memory T cells.
3, 4 and 5 Gy X-ray irradiation combined with 5×10 pan-T cell injection could successfully induce acquired aplastic anemia through T lymphocyte hyperfunction. Compared with 4, 5 Gy irradiated AA group, the 3 Gy irradiated AA group shows significantly longer survival time, and the peripheral blood routine profile closely resembles the clinical manifestations of AA patients.
摘要目的:建立获得性再生障碍性贫血动物模型,以研究T淋巴细胞的功能及再生障碍性贫血(AA)的发病机制和治疗方法。
通过X射线照射联合淋巴细胞注射建立获得性再生障碍性贫血小鼠模型。AA组:从C57BL/6J小鼠脾脏中富集纯化的全T淋巴细胞,经尾静脉注射到小鼠体内(5×10),对CB6F1小鼠进行3、4和5 Gy的X射线照射;全身照射(TBI)组:对CB6F1小鼠进行3、4和5 Gy的X射线照射,并注射相同体积的PBS缓冲液;对照组:仅对CB6F1小鼠注射相同体积的PBS缓冲液。检测外周血常规并计算骨髓有核细胞数量;检查骨髓造血变化;采用流式细胞术检测骨髓中T淋巴细胞的分布,并检测骨髓细胞凋亡及脾脏T淋巴细胞分化情况。
与AA组中接受4、5 Gy照射的小鼠相比,接受3 Gy照射的AA组小鼠存活时间显著延长。3、4和5 Gy X射线照射联合全T淋巴细胞注射可成功诱导红细胞、血液中性粒细胞和血小板严重减少,骨髓有核细胞严重减少,严重的骨髓造血功能衰竭,以及骨髓中T淋巴细胞比例显著增加。CD4和CD8 T细胞均增加,但主要是CD8 T细胞增加,且可促进T细胞从初始T细胞向效应记忆T细胞分化。
3、4和5 Gy X射线照射联合5×10全T细胞注射可通过T淋巴细胞功能亢进成功诱导获得性再生障碍性贫血。与接受4、5 Gy照射的AA组相比,接受3 Gy照射的AA组存活时间显著更长,外周血常规特征与AA患者临床表现极为相似。