Inflammation and Fibrosis in Progeria: Organ-Specific Responses in an HGPS Mouse Model

• Published in: International journal of molecular sciences 2024-08, Vol.25 (17), p.9323
• Main Authors: Krüger, Peter, Schroll, Moritz, Fenzl, Felix, Lederer, Eva-Maria, Hartinger, Ramona, Arnold, Rouven, Cagla Togan, Deniz, Guo, Runjia, Liu, Shiyu, Petry, Andreas, Görlach, Agnes, Djabali, Karima
• Format: Article
• Language: English
• Subjects: Aging; Amino acids; Animals; Cardiovascular disease; Collagen; Coronary vessels; Cytokines; Disease Models, Animal; DNA damage; Fibroblasts; Fibrosis; Genotype & phenotype; Hutchinson–Gilford Progeria Syndrome; Hypoglycemia; Inflammation; Inflammation - metabolism; Inflammation - pathology; Investigations; Laboratories; lamin A; Lamin Type A - genetics; Lamin Type A - metabolism; Lung - metabolism; Lung - pathology; Mice; Musculoskeletal system; Organ Specificity; Pathology; Progeria - genetics; Progeria - metabolism; Progeria - pathology; progerin; Smooth muscle; Spleen; Thymus gland
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25179323

Hutchinson-Gilford Progeria Syndrome (HGPS) is an extremely rare genetic disorder that causes accelerated aging, due to a pathogenic variant in the LMNA gene. This pathogenic results in the production of progerin, a defective protein that disrupts the nuclear lamina's structure. In our study, we conducted a histopathological analysis of various organs in the Lmna mouse model, which is commonly used to study HGPS. The objective of this study was to show that progerin accumulation drives systemic but organ-specific tissue damage and accelerated aging phenotypes. Our findings show significant fibrosis, inflammation, and dysfunction in multiple organ systems, including the skin, cardiovascular system, muscles, lungs, liver, kidneys, spleen, thymus, and heart. Specifically, we observed severe vascular fibrosis, reduced muscle regeneration, lung tissue remodeling, depletion of fat in the liver, and disruptions in immune structures. These results underscore the systemic nature of the disease and suggest that chronic inflammation and fibrosis play crucial roles in the accelerated aging seen in HGPS. Additionally, our study highlights that each organ responds differently to the toxic effects of progerin, indicating that there are distinct mechanisms of tissue-specific damage.