无血清质量和数量控制培养提高结缔组织疾病患者外周血单个核细胞的血管生成潜能

Journal of plastic and reconstructive surgery Pub Date : 2024-05-10 eCollection Date: 2024-10-27 DOI:10.53045/jprs.2022-0050
Satomi Furukawa, Rie Hirano, Ai Sugawara, Satoshi Fujimura, Rica Tanaka
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引用次数: 0

摘要

目的:结缔组织疾病患者内皮祖细胞数量和质量下降。这限制了单个核细胞治疗与结缔组织疾病相关的缺血性溃疡的疗效。为了克服这些问题,我们开发了一种无血清质量和数量控制培养方法,可能提高内皮祖细胞的功能并增加其数量。在这里,我们展示了质量和数量控制培养对结缔组织疾病患者单核细胞的影响。方法:分离C57BL/6JJmsSlc-lpr/lpr小鼠、结缔组织疾病患者和健康志愿者外周血单个核细胞。采用质控定量培养法培养单个核细胞,采用流式细胞术、内皮祖细胞培养法和内皮祖细胞集落形成法分析内皮祖细胞数量。流式细胞术也用于检测单个核细胞亚群。采用人脐静脉内皮细胞成管实验,观察培养的单核细胞的质、量控制功能。结果:系统性红斑狼疮小鼠内皮祖细胞数量明显减少,经质量和数量控制培养后,内皮祖细胞数量与对照组持平。在人体中,健康志愿者和结缔组织疾病患者经过质控和量控培养后,内皮祖细胞和M2巨噬细胞数量明显增加,促炎细胞数量明显减少。人脐静脉内皮细胞成管实验显示,结缔组织疾病患者培养的质量和数量控制的单个核细胞比质量和数量控制的健康对照组培养的单个核细胞有更高的血管生成潜力。结论:质控量培养法能有效恢复结缔组织病患者单核细胞的血管生成能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum-free Quality and Quantity Control Culture Improves the Angiogenic Potential of Peripheral Blood Mononuclear Cells Harvested from Patients with Connective Tissue Diseases.

Objectives: The number and quality of endothelial progenitor cells decrease in patients with connective tissue diseases. This limits the efficacy of mononuclear cell therapy for ischemic ulcers associated with connective tissue diseases. To overcome these problems, we developed a serum-free quality and quantity control culture method that potentially improves the function of endothelial progenitor cells and expands their numbers. Here, we show the effect of quality and quantity control culture on mononuclear cells from patients with connective tissue diseases.

Methods: Peripheral blood mononuclear cells were isolated from C57BL/6JJmsSlc-lpr/lpr mice with systemic lupus erythematosus, patients with connective tissue diseases, and healthy volunteers. Mononuclear cells were cultured using the quality and quantity control culture method, and the number of endothelial progenitor cells was analyzed using flow cytometry, an endothelial progenitor cell culture assay, and an endothelial progenitor cell colony-forming assay. Flow cytometry was also used to examine mononuclear cell subpopulations. A human umbilical vein endothelial cell tube-forming assay was used to examine the function of quality and quantity control cultured mononuclear cells.

Results: Mice with systemic lupus erythematosus showed a significantly lower number of endothelial progenitor cells, which increased to the same levels as those of the control mice after quality and quantity control culture. In humans, the numbers of endothelial progenitor cells and M2 macrophages were significantly increased and the number of proinflammatory cells was decreased after quality and quantity control culture in both healthy volunteers and patients with connective tissue diseases. The human umbilical vein endothelial cell tube formation assay showed higher angiogenic potential in quality and quantity control cultured mononuclear cells from patients with connective tissue diseases than that in quality and quantity control cultured mononuclear cells from healthy controls.

Conclusions: Our study suggests that the quality and quantity control culture method is effective in recovering the angiogenic ability of mononuclear cells from patients with connective tissue diseases.

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