Suppr超能文献

白血病细胞浸润部分通过 MIP-1α/CCL3 导致红细胞生成缺陷。

Leukemia cell infiltration causes defective erythropoiesis partially through MIP-1α/CCL3.

机构信息

State Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Tianjin, China.

Center for Stem Cell Medicine, Tianjin, China.

出版信息

Leukemia. 2016 Sep;30(9):1897-908. doi: 10.1038/leu.2016.81. Epub 2016 Apr 25.

Abstract

Leukemia often results in severe anemia, which may significantly contribute to patient mortality and morbidity. However, the mechanisms underlying defective erythropoiesis in leukemia have not been fully elucidated. In this study, we demonstrated that insufficient erythropoiesis in an immunocompetent acute myeloid leukemia (AML) murine model was due to reduced proliferation of megakaryocyte erythroid progenitors and increased apoptosis of erythroblasts. Colony-forming cell assays indicated that the leukemic bone marrow (BM) plasma inhibited erythroid colony formation, whereas they had no inhibitory effect on other types of colonies. Cytokine array analysis demonstrated that the chemokine CCL3 was elevated in the plasma of AML mice and patients. CCL3 inhibited erythroid differentiation of hematopoietic stem cells, common myeloid progenitors and especially megakaryocytic-erythroid progenitors. Administration of the CCR1 antagonist partially recovered the yield of erythroid colonies in the presence of CCL3 or leukemic BM plasma. Mechanistically, we observed an increase of p38 phosphorylation and subsequent downregulation of GATA1 after CCL3 treatment. Furthermore, knockdown of CCL3 attenuated leukemic progression and alleviated anemia. Therefore, our results demonstrate that elevated CCL3 in the leukemic environment suppresses erythropoiesis via CCR1-p38 activation, suggesting a novel mechanism for the erythroid defects observed in leukemia.

摘要

白血病常导致严重贫血,这可能显著增加患者的死亡率和发病率。然而,白血病中红细胞生成缺陷的机制尚未完全阐明。在本研究中,我们证明免疫功能正常的急性髓系白血病(AML)小鼠模型中,红细胞生成不足是由于巨核细胞-红系祖细胞增殖减少和红细胞前体细胞凋亡增加所致。集落形成细胞分析表明,白血病骨髓(BM)血浆抑制红细胞集落形成,而对其他类型的集落没有抑制作用。细胞因子阵列分析表明,趋化因子 CCL3 在 AML 小鼠和患者的血浆中升高。CCL3 抑制造血干细胞、共同髓系祖细胞,特别是巨核细胞-红系祖细胞的红细胞分化。在 CCL3 或白血病 BM 血浆存在的情况下,CCR1 拮抗剂的给药部分恢复了红细胞集落的产量。在机制上,我们观察到 CCL3 处理后 p38 磷酸化增加,随后 GATA1 下调。此外,CCL3 的敲低减轻了白血病的进展并缓解了贫血。因此,我们的结果表明,白血病环境中升高的 CCL3 通过 CCR1-p38 激活抑制红细胞生成,提示了白血病中观察到的红细胞缺陷的新机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验