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铁和锌金属离子对硅钒钙石生物陶瓷骨免疫调节的不同机制。

Distinct mechanisms of iron and zinc metal ions on osteo-immunomodulation of silicocarnotite bioceramics.

作者信息

Deng Fanyan, Han Xianzhuo, Ji Yingqi, Jin Ying, Shao Yiran, Zhang Jingju, Ning Congqin

机构信息

The Education Ministry Key Lab of Resource Chemistry and Shanghai Frontiers Science Center of Biomimetic Catalysis and Shanghai Engineering Research Center of Green Energy Chemical Engineering, Shanghai Normal University, Shanghai, China.

Department of Stomatology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, No.100 Haining Road, Shanghai 200080, PR China.

出版信息

Mater Today Bio. 2024 May 6;26:101086. doi: 10.1016/j.mtbio.2024.101086. eCollection 2024 Jun.

Abstract

The immunomodulatory of implants have drawn more and more attention these years. However, the immunomodulatory of different elements on the same biomaterials have been rarely investigated. In this work, two widely used biosafety elements, iron and zinc added silicocarnotite (Ca(PO)SiO, CPS) were applied to explore the routine of elements on immune response. The immune reactions over time of Fe-CPS and Zn-CPS were explored at genetic level and protein level, and the effects of their immune microenvironment with different time points on osteogenesis were also investigated in depth. The results confirmed that both Fe-CPS and Zn-CPS had favorable ability to secret anti-inflammatory cytokines. The immune microenvironment of Fe-CPS and Zn-CPS also could accelerate osteogenesis and osteogenic differentiation and . In terms of mechanism, RNA-seq analysis and Western-blot experiment revealed that PI3K-Akt signaling pathway and JAK-STAT signaling pathways were activated of Fe-CPS to promote macrophage polarization from M1 to M2, and its immune microenvironment induced osteogenic differentiation through the activation of Hippo signaling pathway. In comparison, Zn-CPS inhibited polarization of M1 macrophage via the up-regulation of Rap1 signaling pathway and complement and coagulation cascade pathway, while its osteogenic differentiation related pathway of immune environment was NF-κB signaling pathway.

摘要

近年来,植入物的免疫调节作用越来越受到关注。然而,同一生物材料上不同元素的免疫调节作用却鲜有研究。在这项工作中,应用了两种广泛使用的生物安全元素,即添加铁和锌的硅钙石(Ca(PO)SiO,CPS),以探索元素对免疫反应的影响规律。在基因水平和蛋白质水平上研究了Fe-CPS和Zn-CPS随时间的免疫反应,并深入研究了它们在不同时间点的免疫微环境对成骨的影响。结果证实,Fe-CPS和Zn-CPS都具有分泌抗炎细胞因子的良好能力。Fe-CPS和Zn-CPS的免疫微环境也能加速成骨和成骨分化。在机制方面,RNA-seq分析和Western-blot实验表明,Fe-CPS激活PI3K-Akt信号通路和JAK-STAT信号通路,促进巨噬细胞从M1向M2极化,其免疫微环境通过激活Hippo信号通路诱导成骨分化。相比之下,Zn-CPS通过上调Rap1信号通路以及补体和凝血级联途径抑制M1巨噬细胞的极化,而其免疫环境的成骨分化相关途径是NF-κB信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf13/11098954/53a36ae2365c/ga1.jpg

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