LIPE-related lipodystrophic syndrome: clinical features and disease modeling using adipose stem cells

脂肪营养不良 脂肪组织 脂肪细胞 内科学 生物 内分泌学 脂解 病理 胰岛素抵抗 医学 糖尿病 遗传学 病毒载量 病毒 抗逆转录病毒疗法
作者
Camille Sollier,Émilie Capel,C. Aguilhon,Vasily Smirnov,Martine Auclair,Claire Douillard,Miriam Ladsous,Sabine Defoort‐Dhellemmes,Jennifer Gorwood,Laura Braud,Roberto Motterlini,Camille Vatier,Olivier Lascols,Éric Renard,Corinne Vigouroux,Isabelle Jéru
出处
期刊:European journal of endocrinology [Bioscientifica]
卷期号:184 (1): 155-168 被引量:25
标识
DOI:10.1530/eje-20-1013
摘要

The term Multiple Symmetric Lipomatosis (MSL) describes a heterogeneous group of rare monogenic disorders and multifactorial conditions, characterized by upper-body adipose masses. Biallelic variants in LIPE encoding hormone-sensitive lipase (HSL), a key lipolytic enzyme, were implicated in three families worldwide. We aimed to further delineate LIPE-related clinical features and pathophysiological determinants.A gene panel was used to identify pathogenic variants. The disease features were reviewed at the French lipodystrophy reference center. The immunohistological, ultrastructural, and protein expression characteristics of lipomatous tissue were determined in surgical samples from one patient. The functional impact of variants was investigated by developing a model of adipose stem cells (ASCs) isolated from lipomatous tissue.We identified new biallelic LIPE null variants in three unrelated patients referred for MSL and/or partial lipodystrophy. The hallmarks of the disease, appearing in adulthood, included lower-limb lipoatrophy, upper-body and abdominal pseudo-lipomatous masses, diabetes and/or insulin resistance, hypertriglyceridemia, liver steatosis, high blood pressure, and neuromuscular manifestations. Ophthalmological investigations revealed numerous auto-fluorescent drusen-like retinal deposits in all patients. Lipomatous tissue and patient ASCs showed loss of HSL and decreased expression of adipogenic and mature adipocyte markers. LIPE-mutated ASCs displayed impaired adipocyte differentiation, decreased insulin response, defective lipolysis, and mitochondrial dysfunction.Biallelic LIPE null variants result in a multisystemic disease requiring multidisciplinary care. Loss of HSL expression impairs adipocyte differentiation, consistent with the lipodystrophy/MSL phenotype and associated metabolic complications. Detailed ophthalmological examination could reveal retinal damage, further pointing to the nervous tissue as an important disease target.
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