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转录谱分析揭示了特发性声门下气管狭窄的纤维化特征。

Transcriptional profiling sheds light on the fibrotic aspects of idiopathic subglottic tracheal stenosis.

作者信息

Direder Martin, Laggner Maria, Copic Dragan, Klas Katharina, Bormann Daniel, Schweiger Thomas, Hoetzenecker Konrad, Aigner Clemens, Ankersmit Hendrik Jan, Mildner Michael

机构信息

Laboratory for Cardiac and Thoracic Diagnosis, Regeneration and Applied Immunology, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.

Aposcience AG, Vienna, Austria.

出版信息

Front Cell Dev Biol. 2024 Jul 12;12:1380902. doi: 10.3389/fcell.2024.1380902. eCollection 2024.

Abstract

Idiopathic subglottic stenosis (ISGS) is a rare fibrotic disease of the upper trachea with an unknown pathomechanism. It typically affects adult Caucasian female patients, leading to severe airway constrictions caused by progressive scar formation and inflammation with clinical symptoms of dyspnoea, stridor and potential changes to the voice. Endoscopic treatment frequently leads to recurrence, whereas surgical resection and reconstruction provides excellent long-term functional outcome. This study aimed to identify so far unrecognized pathologic aspects of ISGS using single cell RNA sequencing. Our scRNAseq analysis uncovered the cellular composition of the subglottic scar tissue, including the presence of a pathologic, profibrotic fibroblast subtype and the presence of Schwann cells in a profibrotic state. In addition, a pathology-associated increase of plasma cells was identified. Using extended bioinformatics analyses, we decoded pathology-associated changes of factors of the extracellular matrix. Our data identified ongoing fibrotic processes in ISGS and provide novel insights on the contribution of fibroblasts, Schwann cells and plasma cells to the pathogenesis of ISGS. This knowledge could impact the development of novel approaches for diagnosis and therapy of ISGS.

摘要

特发性声门下狭窄(ISGS)是一种罕见的上呼吸道纤维化疾病,其发病机制不明。它通常影响成年白人女性患者,导致由进行性瘢痕形成和炎症引起的严重气道狭窄,伴有呼吸困难、喘鸣等临床症状以及声音的潜在变化。内镜治疗常导致复发,而手术切除和重建可提供良好的长期功能预后。本研究旨在通过单细胞RNA测序确定ISGS迄今未被认识的病理学特征。我们的单细胞RNA测序分析揭示了声门下瘢痕组织的细胞组成,包括一种病理性、促纤维化的成纤维细胞亚型的存在以及处于促纤维化状态的施万细胞的存在。此外,还确定了与病理相关的浆细胞增加。通过扩展的生物信息学分析,我们解码了细胞外基质因子与病理相关的变化。我们的数据确定了ISGS中持续存在的纤维化过程,并为成纤维细胞、施万细胞和浆细胞在ISGS发病机制中的作用提供了新的见解。这些知识可能会影响ISGS诊断和治疗新方法的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d68/11272577/b46b2ef42e1c/fcell-12-1380902-g001.jpg

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