Department of Plastic, Aesthetic and Reconstructive Microsurgery/Hand Surgery, Hospital Ernst von Bergmann, Potsdam, Germany.
Department of Adipocyte Development and Nutrition, German Institute of Human Nutrition (DIfE) Potsdam-Rehbrücke, Nuthetal, Germany.
Front Immunol. 2023 Jul 28;14:1223264. doi: 10.3389/fimmu.2023.1223264. eCollection 2023.
Lipedema is a painful subcutaneous adipose tissue (SAT) disease characterized by adipocyte hypertrophy, immune cell recruitment, and fibrosis in the affected areas. These features are thought to contribute to the development and progression of the condition. However, the relationship between lipedema disease stage and the associated adipose tissue changes has not been determined so far.
SAT biopsies of 32 lipedema patients, ranging across the pathological stages I to III, and 14 BMI- and age-matched controls were harvested from lipedema-affected thighs and non-symptomatic lower abdominal regions. Histological and immunohistochemical (IHC) staining and expression analysis of markers for adipogenesis, immunomodulation, and fibrosis were performed on the tissue biopsies.
Lipedema patients showed increased adipocyte areas and a stage-dependent shift towards larger cell sizes in the thighs. Lipedema SAT was linked with increased interstitial collagen accumulation in the thighs, but not the lower abdominal region when compared to controls. There was a trend toward progressive SAT fibrosis of the affected thighs with increasing lipedema stage. Elevated gene expression levels of macrophage markers were found for thigh SAT biopsies, but not in the abdominal region. IHC staining of lipedema thigh biopsies confirmed a transiently elevated macrophage polarization towards an M2-like (anti-inflammatory) phenotype.
In summary, lipedema SAT is associated with stage-dependent adipocyte hypertrophy, stage-progressive interstitial fibrosis and elevated proportion of M2-like macrophages. The character of the inflammatory response differs from primary obesity and may possess an essential role in the development of lipedema.
脂肪营养不良是一种疼痛的皮下脂肪组织(SAT)疾病,其特征是脂肪细胞肥大、免疫细胞募集和受影响区域的纤维化。这些特征被认为是导致疾病发展和进展的原因。然而,脂肪营养不良疾病阶段与相关脂肪组织变化之间的关系尚未确定。
从脂肪营养不良患者的大腿受影响区域和非症状性下腹部区域采集了 32 名脂肪营养不良患者和 14 名 BMI 和年龄匹配的对照者的 SAT 活检。对组织活检进行了组织学和免疫组织化学(IHC)染色以及脂肪生成、免疫调节和纤维化标志物的表达分析。
脂肪营养不良患者的大腿脂肪细胞面积增加,并且细胞大小随着疾病阶段的进展而增大。与对照组相比,脂肪营养不良患者的大腿 SAT 与间质胶原积累增加有关,但在下腹部区域则没有。随着脂肪营养不良阶段的增加,受影响的大腿 SAT 纤维化呈渐进趋势。大腿 SAT 活检的巨噬细胞标志物基因表达水平升高,但在腹部区域则没有。脂肪营养不良大腿活检的 IHC 染色证实,巨噬细胞向 M2 样(抗炎)表型的极化呈一过性升高。
总之,脂肪营养不良 SAT 与疾病阶段相关的脂肪细胞肥大、阶段进展性间质纤维化和升高的 M2 样巨噬细胞比例有关。炎症反应的特征与原发性肥胖不同,可能在脂肪营养不良的发展中具有重要作用。