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磷酸钙微球的免疫调节作用:粒径对巨噬细胞极化和分泌模式的影响

Immunomodulatory effects of calcium phosphate microspheres: influences of particle size on macrophage polarization and secretion patterns.

作者信息

Wan Qiwen, Tian Luoqiang, Wang Menglu, Chen Fuying, Li Xiangfeng, Xiao Yumei, Chen Xuening, Zhang Xingdong

机构信息

National Engineering Research Center for Biomaterials, College of Biomedical Engineering, Sichuan University, Chengdu, 610064, China.

Research Center for Material Genome Engineering, Sichuan University, Chengdu, 610064, China.

出版信息

J Mater Chem B. 2025 Jan 2;13(2):549-561. doi: 10.1039/d4tb02249a.

Abstract

This study investigated the immunomodulatory effects of calcium phosphate (CaP) microspheres, focusing on how particle size influenced macrophage polarization and cytokine secretion patterns. SEM analysis revealed that HA microspheres predominantly exhibited a spherical shape with distinct sizes and sub-micro-sized pores. The average particle sizes for the S1, S2, and S3 groups were 17.36 μm, 27.59 μm, and 47.14 μm, respectively. experiments demonstrated that small-sized S1 microspheres were more readily phagocytosed by macrophages, leading to a pro-inflammatory M1 phenotype characterized by increased gene expression of iNos and inflammatory cytokines (IL-1β, IL-6, TNF-α), and a higher proportion of CCR7 M1 macrophages. In contrast, the larger S2 and S3 microspheres favored an anti-inflammatory M2 phenotype, with higher expression of Arg and anti-inflammatory cytokines (IL-10), and greater proportions of CD206 M2 macrophages. Additionally, HA microspheres were injected into mouse quadriceps muscles, revealing significant differences in immune cell infiltration and tissue response. The S1 microspheres induced a prolonged and more severe inflammatory response, while the S2 and S3 microspheres were embedded in cell-rich tissue with minimal inflammation or fibrosis. It indicated the potential of larger microspheres (S2 and S3) to create a more favorable immune microenvironment that supported faster and more effective tissue healing. These findings underscore the importance of optimizing microsphere size to achieve desired immunomodulatory effects, thereby enhancing their clinical efficacy.

摘要

本研究调查了磷酸钙(CaP)微球的免疫调节作用,重点关注粒径如何影响巨噬细胞极化和细胞因子分泌模式。扫描电子显微镜(SEM)分析显示,羟基磷灰石(HA)微球主要呈球形,具有不同的尺寸和亚微米级孔隙。S1、S2和S3组的平均粒径分别为17.36μm、27.59μm和47.14μm。实验表明,小尺寸的S1微球更容易被巨噬细胞吞噬,导致促炎M1表型,其特征是诱导型一氧化氮合酶(iNos)和炎性细胞因子(白细胞介素-1β、白细胞介素-6、肿瘤坏死因子-α)的基因表达增加,以及CCR7 M1巨噬细胞比例更高。相比之下,较大的S2和S3微球有利于抗炎M2表型,具有更高的精氨酸酶(Arg)和抗炎细胞因子(白细胞介素-10)表达,以及更高比例的CD206 M2巨噬细胞。此外,将HA微球注射到小鼠股四头肌中,发现免疫细胞浸润和组织反应存在显著差异。S1微球诱导了持续时间更长、更严重的炎症反应,而S2和S3微球则嵌入富含细胞的组织中,炎症或纤维化程度最小。这表明较大的微球(S2和S3)有可能创造一个更有利的免疫微环境,支持更快、更有效的组织愈合。这些发现强调了优化微球尺寸以实现所需免疫调节作用从而提高其临床疗效的重要性。

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