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利拉鲁肽通过在体外抑制M1巨噬细胞极化和CXCL9释放来促进间充质干细胞的成骨分化。

Liraglutide promotes osteogenic differentiation of mesenchymal stem cells by inhibiting M1 macrophage polarization and CXCL9 release in vitro.

作者信息

He Yilin, Song Wenpeng, Deng Yinxin, Lin Xiao, Gao Zhenhua, Ma Pan

机构信息

Implant Department, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Tiantan Xili No.4, Dongcheng District, Beijing, 100050, China.

Department of Stomatology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.

出版信息

Mol Cell Endocrinol. 2025 Feb 1;597:112441. doi: 10.1016/j.mce.2024.112441. Epub 2024 Dec 18.

Abstract

As a GLP-1 receptor agonist widely used in treating type 2 diabetes, liraglutide shows potential applications in bone tissue engineering. This study investigated liraglutide's direct effects on rat bone marrow mesenchymal stem cells (BMSCs) osteogenic differentiation and its regulatory mechanism through macrophage polarization. Results showed that liraglutide significantly enhanced BMSC migration and osteogenic differentiation. Additionally, liraglutide markedly inhibited M1 macrophage polarization induced by LPS and IFN-γ, reducing inflammatory factors CXCL9 and TNF-α secretion, possibly by partially reversing M1 macrophage regulatory signals (AMPK and NF-κB pathways). Compared to M1 macrophage-conditioned medium (M1-CM), conditioned medium from liraglutide-treated macrophages showed stronger promotion of BMSC osteogenic differentiation, though this effect was reversed by CXCL9 addition. The study demonstrates that liraglutide enhances BMSC osteogenic capacity both directly and by inhibiting M1 macrophage polarization and CXCL9 secretion, offering a new therapeutic option for severe bone defects with inflammatory responses.

摘要

作为一种广泛用于治疗2型糖尿病的胰高血糖素样肽-1(GLP-1)受体激动剂,利拉鲁肽在骨组织工程中显示出潜在的应用价值。本研究调查了利拉鲁肽对大鼠骨髓间充质干细胞(BMSCs)成骨分化的直接影响及其通过巨噬细胞极化的调控机制。结果表明,利拉鲁肽显著增强了BMSCs的迁移和成骨分化。此外,利拉鲁肽明显抑制了由脂多糖(LPS)和干扰素-γ(IFN-γ)诱导的M1巨噬细胞极化,减少了炎性因子CXCL9和肿瘤坏死因子-α(TNF-α)的分泌,这可能是通过部分逆转M1巨噬细胞的调控信号(AMPK和核因子-κB(NF-κB)通路)实现的。与M1巨噬细胞条件培养基(M1-CM)相比,利拉鲁肽处理的巨噬细胞的条件培养基对BMSCs成骨分化的促进作用更强,不过添加CXCL9后这种作用被逆转。该研究表明,利拉鲁肽既能直接增强BMSCs的成骨能力,又能通过抑制M1巨噬细胞极化和CXCL9分泌来实现这一目的,为伴有炎症反应的严重骨缺损提供了一种新的治疗选择。

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