| Literature DB >> 35414038 |
Mei Zhou1, Yuexin Zhu2,3, Zeyi Zhou4, Feiran Qi2,3, Shuai Zheng2,3, Shijuan Gao2,3, Yulin Li2,3, Yan Liu5,6, Jie Du7,8,9.
Abstract
Fibrillin 1 (Fbn1) mutation causes Marfan syndrome (MFS) with thoracic aortic aneurysm (TAA) as the main complication. The mechanisms for extracellular matrix (ECM) homeostasis disruption in MFS TAA are unclear. Here, we found ECM-related gene secreted phosphoprotein 1 (Spp1) increased in Fbn1C1041G/+ mice using transcriptome sequencing and a distinct fibroblast subcluster with Spp1 as the strongest marker was identified with analysis of the MFS mouse aortic single-cell sequencing dataset. Immunostaining confirmed elevated Spp1 in adventitial fibroblasts, and Spp1 might regulate fibroblast and smooth muscle cell (SMC) communication primarily through Itga8/Itgb1. Then, we observed Spp1 reduced contractile genes Acta2 and Tagln expression in SMCs and increased collagen expression in fibroblasts, which might contribute to TAA development. Finally, we also found elevated SPP1 plasma level was associated with an increased risk of TAA in patients. Therefore, SPP1 may serve as a biomarker and therapeutic target for TAA.Entities:
Keywords: Aortic aneurysm; Extracellular matrix; Fibroblast; Marfan syndrome; Secreted phosphoprotein 1
Year: 2022 PMID: 35414038 DOI: 10.1007/s12265-022-10239-8
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 4.132