National Medical Research Center of Hematology, Ministry of Health of the Russian Federation, Moscow, Russia.
Bull Exp Biol Med. 2022 Mar;172(5):637-641. doi: 10.1007/s10517-022-05453-y. Epub 2022 Mar 30.
The properties of bone marrow-derived multipotent mesenchymal stromal cells (MSC) of patients with aplastic anemia at the onset of the disease are studied insufficiently. The aim of this work was to test the ability of MSC from patients with aplastic anemia to maintain hematopoietic precursors and to analyze the expression of genes associated with hematopoiesis and immune response. The ability of MSC to maintain hematopoietic precursors was determined by counting cobblestone area-forming cells; gene expression was analyzed by quantitative PCR. It was shown that MSC of patients with aplastic anemia preserve their ability to maintain hematopoietic precursors. Pronounced changes in the expression of the VEGFA and ANGPT1 genes were found. MSC from aplastic anemia patients with PNH clone significantly differ from those from aplastic anemia patients without PNH clone in terms of the expression of the SDF1, IL1R, and VEGFA genes. Changes in gene expression can be associated with the pathogenesis of the disease.
再生障碍性贫血患者发病时骨髓来源的多能间充质基质细胞(MSC)的特性研究不足。本工作的目的是检测再生障碍性贫血患者 MSC 维持造血前体细胞的能力,并分析与造血和免疫反应相关的基因表达。通过计数鹅卵石区形成细胞来确定 MSC 维持造血前体细胞的能力;通过定量 PCR 分析基因表达。结果表明,再生障碍性贫血患者的 MSC 保持维持造血前体细胞的能力。发现 VEGFA 和 ANGPT1 基因的表达明显改变。伴有 PNH 克隆的再生障碍性贫血患者的 MSC 在 SDF1、IL1R 和 VEGFA 基因的表达方面与不伴有 PNH 克隆的再生障碍性贫血患者的 MSC 显著不同。基因表达的变化可能与疾病的发病机制有关。