Institute of Medical Genetics, Center of Pathobiochemistry and Genetics.
Department of Dermatology, and.
Am J Respir Crit Care Med. 2024 May 1;209(9):1152-1164. doi: 10.1164/rccm.202307-1273OC.
Chronic sarcoidosis is a complex granulomatous disease with limited treatment options that can progress over time. Understanding the molecular pathways contributing to disease would aid in new therapeutic development. To understand whether macrophages from patients with nonresolving chronic sarcoidosis are predisposed to macrophage aggregation and granuloma formation and whether modulation of the underlying molecular pathways influence sarcoidosis granuloma formation. Macrophages were cultivated from isolated peripheral blood CD14 monocytes and evaluated for spontaneous aggregation. Transcriptomics analyses and phenotypic and drug inhibitory experiments were performed on these monocyte-derived macrophages. Human skin biopsies from patients with sarcoidosis and a myeloid -specific sarcoidosis mouse model were analyzed for validatory experiments. Monocyte-derived macrophages from patients with chronic sarcoidosis spontaneously formed extensive granulomas compared with healthy control participants. Transcriptomic analyses separated healthy and sarcoidosis macrophages and identified an enrichment in lipid metabolic processes. patient granulomas, sarcoidosis mouse model granulomas, and those directly analyzed from lesional patient skin expressed an aberrant lipid metabolism profile and contained increased neutral lipids. Conversely, a combination of statins and cholesterol-reducing agents reduced granuloma formation both and in a sarcoidosis mouse model. Together, our findings show that altered lipid metabolism in sarcoidosis macrophages is associated with its predisposition to granuloma formation and suggest cholesterol-reducing therapies as a treatment option in patients.
慢性肉状瘤病是一种复杂的肉芽肿性疾病,治疗选择有限,且病情可能随时间进展。了解导致疾病的分子途径有助于开发新的治疗方法。为了了解非缓解性慢性肉状瘤病患者的巨噬细胞是否容易发生巨噬细胞聚集和肉芽肿形成,以及调节潜在的分子途径是否会影响肉状瘤肉芽肿的形成。从分离的外周血 CD14 单核细胞中培养巨噬细胞,并评估其自发聚集的情况。对这些单核细胞衍生的巨噬细胞进行转录组分析以及表型和药物抑制实验。分析来自肉状瘤病患者的人类皮肤活检和骨髓特异性肉状瘤病小鼠模型以进行验证实验。与健康对照组相比,来自慢性肉状瘤病患者的单核细胞衍生巨噬细胞自发形成广泛的肉芽肿。转录组分析将健康和肉状瘤病巨噬细胞分开,并确定脂质代谢过程的富集。患者的肉芽肿、肉状瘤病小鼠模型的肉芽肿以及直接从病变患者皮肤分析的肉芽肿均表现出异常的脂质代谢谱,并含有增加的中性脂质。相反,他汀类药物和胆固醇降低剂的组合均减少了肉状瘤病小鼠模型中的肉芽肿形成。总之,我们的发现表明,肉状瘤病巨噬细胞中脂质代谢的改变与其易发生肉芽肿形成有关,并提示胆固醇降低疗法可作为患者的一种治疗选择。