β-aminopropionitrile Induces Distinct Pathologies in the Ascending and Descending Thoracic Aortic Regions of Mice

赖氨酰氧化酶 胸主动脉 病理 弹性纤维 管腔(解剖学) 解剖 升主动脉 免疫染色 弹性蛋白 医学 降主动脉 主动脉 内科学 生物 免疫组织化学 细胞外基质 细胞生物学
作者
Michael Franklin,Hisashi Sawada,Sohei Ito,Deborah A. Howatt,Naofumi Amioka,Ching-Ling Liang,Nancy Zhang,David B Graf,Jessica J. Moorleghen,Yuriko Katsumata,Hong Lü,Alan Daugherty
出处
期刊: [Cold Spring Harbor Laboratory]
被引量:1
标识
DOI:10.1101/2023.10.22.563474
摘要

ABSTRACT BACKGROUND β-aminopropionitrile (BAPN) is a pharmacological inhibitor of lysyl oxidase and lysyl oxidase-like proteins. Administration of BAPN promotes aortopathies, although there is a paucity of data on experimental conditions to generate pathology. The objective of this study was to define experimental parameters and determine whether equivalent or variable aortopathies were generated throughout the aortic tree during BAPN administration in mice. METHODS BAPN was administered in drinking water for a period ranging from 1 to 12 weeks. The impacts of BAPN were first assessed with regard to dose, strain, age, and sex. BAPN-induced aortic pathological characterization was conducted using histology and immunostaining. To investigate the mechanistic basis of regional heterogeneity, ascending and descending thoracic aortas were harvested after one week of BAPN administration before the appearance of overt pathology. RESULTS BAPN-induced aortic rupture predominantly occurred or originated in the descending thoracic aorta in young C57BL/6J or N mice. No apparent differences were found between male and female mice. For mice surviving 12 weeks of BAPN administration, profound dilatation was consistently observed in the ascending region, while there were more heterogeneous changes in the descending thoracic region. Pathological features were distinct between the ascending and descending thoracic regions. Aortic pathology in the ascending region was characterized by luminal dilatation and elastic fiber disruption throughout the media. The descending thoracic region frequently had dissections with false lumen formation, collagen deposition, and remodeling of the wall surrounding the false lumen. Cells surrounding the false lumen were predominantly positive for α-smooth muscle actin. One week of BAPN administration compromised contractile properties in both regions equivalently, and RNA sequencing did not show obvious differences between the two aortic regions in smooth muscle cell markers, cell proliferation markers, and extracellular components. CONCLUSIONS BAPN-induced pathologies show distinct, heterogeneous features within and between ascending and descending aortic regions in mice.
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