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人牙囊细胞来源的条件培养基通过调节牙周膜干细胞的成骨分化、炎症反应及巨噬细胞极化来促进牙周再生。

Human dental follicle cell-derived conditioned media enhance periodontal regeneration by regulating the osteogenic differentiation and inflammation of periodontal ligament stem cells and macrophage polarization.

作者信息

Gao Yichen, He Xianyi, Deng Yuyao, Wang Xia, Shen Jie, Xu Wei, Cai Rui, Lan Xiaorong, Chen Junliang, He Yun

机构信息

Department of Oral and Maxillofacial Surgery, The Affiliated Stomatological Hospital, Southwest Medical University, Yunfenglu 10, Luzhou, 646000, China.

Luzhou Key Laboratory of Oral and Maxillofacial Reconstruction and Regeneration, Xianglinlu 1, Luzhou, 646000, China.

出版信息

Mol Cell Biochem. 2025 Apr 2. doi: 10.1007/s11010-025-05260-9.

Abstract

Dental follicle cells (DFCs) derived from the neural crest are promising seed cells for periodontal tissue engineering. This study aimed to investigate whether conditioned media (CM) from human DFCs could regenerate impaired periodontal tissue and the underlying mechanisms. hDFC-derived CM (hDFC-CM) were obtained via ultracentrifugation. In vitro, human periodontal ligament stem cells (hPDLSCs) were treated with hDFC-CM in normal and inflammatory microenvironments, and the cell proliferation, migration, and osteogenic potential were evaluated. We simulated the inflammatory environment with lipopolysaccharide and detected the expression of osteogenic and Wnt/β-catenin signaling pathway-related proteins. The effect of hDFC-CM on the inhibition of hPDLSC inflammation and macrophage polarization was examined. In vivo, the rat periodontitis model was treated with hDFC-CM. Tissue samples were collected after 4 weeks for micro-computed tomography and histological examination. The results of cell counting kit-8 and scratch experiments showed that hDFC-CM significantly enhanced the proliferation and migration capacities of hPDLSCs. hDFC-CM promoted the osteogenic differentiation of hPDLSCs by showing intense alkaline phosphatase and Alizarin Red staining and upregulated osteogenic protein and gene expression. Western blotting also verified that hDFC-CM promotes the osteogenic differentiation of hPDLSCs by regulating the Wnt/β-catenin pathway in an inflammatory environment. In addition, hDFC-CM inhibited hPDLSC inflammation and polarized macrophages from the M1 to M2 phenotype. In vivo, hDFC-CM effectively promoted periodontal tissue regeneration. hDFC-CM enhances periodontal regeneration by regulating the osteogenic differentiation and inflammation of periodontal ligament stem cells and macrophage polarization, which provided new biochemical cues for the treatment of periodontitis.

摘要

源自神经嵴的牙囊细胞(DFCs)是牙周组织工程中有前景的种子细胞。本研究旨在探讨人DFCs的条件培养基(CM)是否能再生受损的牙周组织及其潜在机制。通过超速离心获得hDFC衍生的CM(hDFC-CM)。在体外,将人牙周膜干细胞(hPDLSCs)在正常和炎症微环境中用hDFC-CM处理,并评估细胞增殖、迁移和成骨潜能。我们用脂多糖模拟炎症环境,检测成骨和Wnt/β-连环蛋白信号通路相关蛋白的表达。检测hDFC-CM对hPDLSC炎症抑制和巨噬细胞极化的影响。在体内,用hDFC-CM治疗大鼠牙周炎模型。4周后收集组织样本进行显微计算机断层扫描和组织学检查。细胞计数试剂盒-8和划痕实验结果表明,hDFC-CM显著增强了hPDLSCs的增殖和迁移能力。hDFC-CM通过强烈的碱性磷酸酶和茜素红染色以及上调成骨蛋白和基因表达,促进了hPDLSCs的成骨分化。蛋白质免疫印迹法也证实,hDFC-CM在炎症环境中通过调节Wnt/β-连环蛋白通路促进hPDLSCs的成骨分化。此外,hDFC-CM抑制hPDLSC炎症,并使巨噬细胞从M1型极化为M2型。在体内,hDFC-CM有效地促进了牙周组织再生。hDFC-CM通过调节牙周膜干细胞的成骨分化和炎症以及巨噬细胞极化来增强牙周再生,这为牙周炎的治疗提供了新的生化线索。

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