Laboratory of Stem Cells and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China.
Laboratory of Stem Cells and Tissue Engineering, Department of Histology and Embryology, Chongqing Medical University, Chongqing 400016, China.
Int Immunopharmacol. 2024 Dec 5;142(Pt A):113061. doi: 10.1016/j.intimp.2024.113061. Epub 2024 Sep 12.
Chronic anemia, especially chemotherapy-induced anemia, is a common and intractable symptom. Puzzlingly, the conventional anemic treatment may lead to various side effects, and the mechanism of stress anemia remains unclear.
Here, peripheral blood, histopathological and transmission electron microscopical examination, colony forming test, flow cytometry, and qRT-PCR assay were used to investigate the effects of Angelia sinensis polysaccharide (ASP), one main active ingredient of Chinese herb medicine Angelica sinensis, on ameliorating 5-fluorouracil (5-FU)-induced stress anemia.
We found that intraperitoneal injection to a C57BL/6J mouse ASP 100 mg/kg per day for consecutive 10 days or 14 days, remarkably accelerated the recovery of RBC, hemoglobin, and hematocrit in blood. ASP alleviated 5-FU-caused impairment of bone marrow cell and BFU-E enumeration. Meanwhile, ASP antagonized 5-FU promoting extramedullary erythropoiesis in the spleen, inducing splenomegaly due to stress erythroblastic islands, and occurrence of megakaryocytes and hematopoietic precursors in splenic colonies. ASP increased splenic stress BFU-E enumeration, driving BFU-E differentiation towards Pro-E and end-stage erythroblasts. Furthermore, ASP increased the number of F4/80VCAM-1 splenic erythroblastic island central macrophages, upregulating genetic expression of EPOR, Emp, VCAM-1, Hmox-1, Trf, TfR1, Fpn1, Spi-C, DNase2a, Tim4, MertK, and Klf1 in splenocytes.
Our findings indicate that the possible mechanism of chemotherapy-induced anemia is related to stress erythroid maturation arrest. Whereas, ASP may promote stress erythroid differentiation via elevated EPO sensitivity in extramedullary hematopoietic organs and enhanced macrophage-mediated adhesion, iron homeostasis and transfer, and nuclear engulfment, which may represent a promising therapeutic strategy.
慢性贫血,特别是化疗引起的贫血,是一种常见且棘手的症状。令人困惑的是,传统的贫血治疗方法可能会导致各种副作用,而应激性贫血的发病机制尚不清楚。
本研究采用外周血、组织病理学和透射电镜检查、集落形成试验、流式细胞术和 qRT-PCR 检测等方法,研究了中药当归主要活性成分当归多糖(ASP)对改善 5-氟尿嘧啶(5-FU)诱导的应激性贫血的作用。
我们发现,连续 10 天或 14 天腹腔注射 C57BL/6J 小鼠 100mg/kg ASP,可显著加快 RBC、血红蛋白和血细胞比容的恢复。ASP 减轻了 5-FU 引起的骨髓细胞损伤和 BFU-E 计数减少。同时,ASP 拮抗了 5-FU 促进脾内骨髓外红细胞生成,导致脾肿大和因应激性红细胞岛而出现巨核细胞和造血前体细胞。ASP 增加了脾内应激性 BFU-E 计数,促进 BFU-E 向 Pro-E 和终末红细胞分化。此外,ASP 增加了 F4/80VCAM-1 脾红细胞岛中央巨噬细胞的数量,上调了脾细胞中 EPOR、Emp、VCAM-1、Hmox-1、Trf、TfR1、Fpn1、Spi-C、DNase2a、Tim4、MertK 和 Klf1 的基因表达。
本研究结果表明,化疗引起的贫血的可能机制与应激性红细胞成熟阻滞有关。而 ASP 可能通过提高骨髓外造血器官中 EPO 的敏感性,增强巨噬细胞介导的黏附、铁稳态和转运以及核吞噬作用,促进应激性红细胞分化,这可能代表一种有前途的治疗策略。