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脂肪性水肿:一种由M2极化巨噬细胞引发的疾病?

Lipedema: A Disease Triggered by M2 Polarized Macrophages?

作者信息

Grewal Thomas, Kempa Sally, Buechler Christa

机构信息

School of Pharmacy, Faculty of Medicine and Health, University of Sydney, Sydney, NSW 2006, Australia.

Department of Plastic, Hand, and Reconstructive Surgery, University Hospital Regensburg, 93053 Regensburg, Germany.

出版信息

Biomedicines. 2025 Feb 23;13(3):561. doi: 10.3390/biomedicines13030561.

Abstract

: Lipedema is a progressive disease that results in the bilateral and symmetrical accumulation of subcutaneous fat in the legs and/or arms, affecting almost exclusively women. : A comprehensive review of the peer-reviewed literature was conducted between November 2024 and February 2025. : The pathophysiology of lipedema is complex and, especially in the early stages, shows similarities to obesity, involving adipocytes, adipose tissue-resident macrophages, and endothelial cells. In lipedema, systemic levels and the adipocyte expression of the classical adipokines adiponectin and leptin appear normal, while it remains unclear if markers of inflammation and oxidative stress are increased. Macrophages in the adipose tissue of patients have an anti-inflammatory M2 phenotype and express high levels of the scavenger receptor CD163. These cells affect adipogenesis and seem to have a central role in adipose tissue accumulation. Increased lymphatic and blood vessel permeability are comorbidities of lipedema that occur in early disease states and may contribute to disease progression. : This review summarizes our current understanding of the pathophysiology of lipedema with a focus on the role of stromal vascular localized M2 macrophages.

摘要

脂肪性水肿是一种进行性疾病,导致腿部和/或手臂双侧对称地堆积皮下脂肪,几乎只影响女性。2024年11月至2025年2月对同行评议文献进行了全面综述。脂肪性水肿的病理生理学很复杂,尤其是在早期,与肥胖有相似之处,涉及脂肪细胞、驻留于脂肪组织的巨噬细胞和内皮细胞。在脂肪性水肿中,经典脂肪因子脂联素和瘦素的全身水平及脂肪细胞表达似乎正常,而炎症和氧化应激标志物是否升高尚不清楚。患者脂肪组织中的巨噬细胞具有抗炎M2表型,并高表达清道夫受体CD163。这些细胞影响脂肪生成,似乎在脂肪组织堆积中起核心作用。淋巴管和血管通透性增加是脂肪性水肿的合并症,发生于疾病早期,可能促进疾病进展。本综述总结了我们目前对脂肪性水肿病理生理学的理解,重点关注基质血管局部M2巨噬细胞的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f59/11940465/927ab77d95ab/biomedicines-13-00561-g001.jpg

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