Department of Biosciences and Nutrition, Karolinska Institutet, 14183, Huddinge, Sweden.
Department of Clinical Science, Intervention and Technology, Division of Renal Medicine, Karolinska Institutet, 14186, Stockholm, Sweden.
Sci Rep. 2017 Jun 30;7(1):4405. doi: 10.1038/s41598-017-04492-0.
Accumulation of progerin is believed to underlie the pathophysiology of Hutchinson-Gilford progeria syndrome, a disease characterized by clinical features suggestive of premature aging, including loss of subcutaneous white adipose tissue (sWAT). Although progerin has been found in cells and tissues from apparently healthy individuals, its significance has been debated given its low expression levels and rare occurrence. Here we demonstrate that sustained progerin expression in a small fraction of preadipocytes and adipocytes of mouse sWAT (between 4.4% and 6.7% of the sWAT cells) results in significant tissue pathology over time, including fibrosis and lipoatrophy. Analysis of sWAT from mice of various ages showed senescence, persistent DNA damage and cell death that preceded macrophage infiltration, and systemic inflammation. Our findings suggest that continuous progerin expression in a small cell fraction of a tissue contributes to aging-associated diseases, the adipose tissue being particularly sensitive.
早衰症是一种以临床特征提示早衰为特征的疾病,目前认为其病理生理学基础是核纤层蛋白病的积累。核纤层蛋白病是由核纤层蛋白基因突变引起的一组罕见的常染色体显性遗传病。尽管已经在来自明显健康个体的细胞和组织中发现了核纤层蛋白病,但由于其低表达水平和罕见发生,其意义一直存在争议。在这里,我们证明在小鼠的皮下白色脂肪组织(sWAT)中的一小部分前脂肪细胞和脂肪细胞中持续表达核纤层蛋白病(占 sWAT 细胞的 4.4%至 6.7%)会导致随着时间的推移出现明显的组织病理学改变,包括纤维化和脂肪萎缩。对来自不同年龄的小鼠的 sWAT 进行分析表明,衰老、持续的 DNA 损伤和细胞死亡先于巨噬细胞浸润和全身炎症。我们的研究结果表明,组织中一小部分细胞持续表达核纤层蛋白病会导致与衰老相关的疾病,脂肪组织尤其敏感。