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巨噬细胞通过调节肌生成和血管生成对舌发育至关重要。

Macrophage is crucial for tongue development by regulating myogenesis and vascularization.

作者信息

Wang Ziyao, Wang Mengqiao, Liu Jiani, Zhao Delu, Wang Jixiao, Wei Fulan

机构信息

Department of Orthodontics, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Center for Oral Diseases, No.44-1 Wenhua Road West, Jinan, Shandong, 250012, China.

出版信息

BMC Oral Health. 2025 May 2;25(1):678. doi: 10.1186/s12903-025-06059-2.

Abstract

BACKGROUND

Abnormal tongue development is a craniofacial deformity that affects dental-maxillofacial esthetics and function. Recent evidence has identified macrophages as multi-functional immune cells crucial for heart and brain development. However, it is still unknown whether macrophages affect tongue development. Therefore, this study aims to assess the distribution, phenotype, and roles of macrophages in the developing tongue.

METHODS

In this study, immunohistochemical (IHC) and multiplex immunofluorescence (mIF) staining were conducted on C57BL/6 mice at embryonic day (E) 13.5, E14.5, E16.5, and E18.5 to analyze the distribution and phenotype of macrophages. Hematoxylin-Eosin (HE), IHC, IF, and mIF staining were also performed on embryonic CX3 CR1-CreERT2; Rosa-DTA conditional macrophage-depleted mice to investigate the effects on fetal tongue development and elucidate mechanisms from myogenesis, vascularization, and cell apoptosis. Statistical significance between the two groups was determined using unpaired two-tailed Student's t-tests. For comparisons involving three or more groups, one-way analysis of variance (ANOVA) followed by Tukey's multiple comparison tests was utilized. A significance level of P < 0.05 was set for statistical significance.

RESULTS

Macrophages were present in the developing tongue from E13.5 to E18.5, with a majority being of the M2 phenotype. Depletion of macrophages resulted in abnormal tongue morphology, decreased tongue height, width, and size, as well as reduced and disorganized muscle fibers. Depletion of macrophages also increased apoptosis. Vascular morphogenesis was impacted, with reductions in the luminal and vascular wall cross-sectional areas of the lingual artery. Vascular endothelial cells were reduced and disorganized with decreased expression of VEGFA and TGF-β1. Moreover, macrophages were located near vascular endothelial cells and secreted pro-angiogenic factors, suggesting their involvement in promoting vascularization.

CONCLUSIONS

Our findings indicate that macrophages play crucial roles in fetal tongue development by affecting myogenesis, cell apoptosis, and vascular growth.

摘要

背景

舌发育异常是一种影响牙颌面美学和功能的颅面畸形。最近的证据表明巨噬细胞是对心脏和大脑发育至关重要的多功能免疫细胞。然而,巨噬细胞是否影响舌发育仍不清楚。因此,本研究旨在评估巨噬细胞在发育中的舌中的分布、表型和作用。

方法

在本研究中,对胚胎期(E)13.5、E14.5、E16.5和E18.5的C57BL/6小鼠进行免疫组织化学(IHC)和多重免疫荧光(mIF)染色,以分析巨噬细胞的分布和表型。还对胚胎期CX3 CR1-CreERT2;Rosa-DTA条件性巨噬细胞耗竭小鼠进行苏木精-伊红(HE)、IHC、IF和mIF染色,以研究对胎儿舌发育的影响,并从肌发生、血管生成和细胞凋亡方面阐明机制。两组之间的统计学显著性采用非配对双尾学生t检验确定。对于涉及三组或更多组的比较,采用单因素方差分析(ANOVA),随后进行Tukey多重比较检验。设定P < 0.05的显著性水平作为统计学显著性标准。

结果

巨噬细胞在E13.5至E18.5的发育中的舌中存在,大多数为M2表型。巨噬细胞的耗竭导致舌形态异常,舌高度、宽度和大小减小,以及肌纤维减少和紊乱。巨噬细胞的耗竭还增加了细胞凋亡。血管形态发生受到影响,舌动脉的管腔和血管壁横截面积减小。血管内皮细胞减少且紊乱,VEGFA和TGF-β1的表达降低。此外,巨噬细胞位于血管内皮细胞附近并分泌促血管生成因子,表明它们参与促进血管生成。

结论

我们的研究结果表明,巨噬细胞通过影响肌发生、细胞凋亡和血管生长在胎儿舌发育中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72e6/12049047/c1c0298d0e30/12903_2025_6059_Fig1_HTML.jpg

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