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特发性声门下狭窄中激素受体表达的细胞区室定位。

Localizing Hormone Receptor Expression to Cellular Compartments in Idiopathic Subglottic Stenosis.

机构信息

Department of Otolaryngology-Head & Neck Surgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Department of Otolaryngology-Head & Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

出版信息

Laryngoscope. 2023 Dec;133(12):3506-3511. doi: 10.1002/lary.30856. Epub 2023 Jun 29.

Abstract

OBJECTIVES

Idiopathic subglottic stenosis (iSGS) is an unexplained progressive fibrosis of the upper airway. iSGS almost exclusively affects women; as a result, female hormones (estrogen and progesterone) have been proposed to participate in the pathogenesis of iSGS. Our aim was to localize cell-specific gene expression of estrogen receptors (ESR1 and ESR2) and progesterone receptor (PGR) using an established iSGS single-cell RNA sequencing (scRNAseq) cell atlas.

STUDY DESIGN

Ex vivo molecular study of airway scar and healthy mucosa from iSGS patients.

METHODS

An established scRNAseq atlas consisting of 25,974 individually sequenced cells from subglottic scar (n = 7) or matched unaffected mucosa (n = 3) in iSGS patients was interrogated for RNA expression of ESR1, ESR2, and PGR. Results were quantified and compared across cell subsets, then visualized using Uniform Manifold Approximation and Projection (UMAP). Confirmatory protein assessment of endocrine receptors in fibroblasts from iSGS patients (n = 5) was performed via flow cytometry.

RESULTS

The proximal airway mucosa in iSGS patients demonstrates differential expression of endocrine receptors (ESR1, ESR2, PGR). Within airway scar, endocrine receptors are primarily expressed by fibroblasts, immune cells, and endothelial cells. Fibroblasts show strong ESR1 and PGR expression, while immune cells possess RNA for both ESR1 and ESR2. Endothelial cells predominantly express ESR2. Epithelial cells in unaffected mucosa express all three receptors, which are all reduced in airway scar.

CONCLUSIONS

scRNAseq data localized endocrine receptor expression to specific cell subsets. These results provide the foundation for future work interrogating how hormone-dependent mechanisms promote, sustain, or participate in iSGS disease pathogenesis.

LEVEL OF EVIDENCE

NA; Basic science Laryngoscope, 133:3506-3511, 2023.

摘要

目的

特发性声门下狭窄(iSGS)是一种不明原因的上呼吸道进行性纤维化。iSGS 几乎仅影响女性;因此,有人提出女性激素(雌激素和孕激素)可能参与 iSGS 的发病机制。我们的目的是使用已建立的 iSGS 单细胞 RNA 测序(scRNAseq)细胞图谱定位雌激素受体(ESR1 和 ESR2)和孕激素受体(PGR)的细胞特异性基因表达。

研究设计

对 iSGS 患者气道瘢痕和健康黏膜的离体分子研究。

方法

对来自 iSGS 患者声门下瘢痕(n=7)或匹配的无病变黏膜(n=3)的 25974 个单独测序细胞的已建立 scRNAseq 图谱进行 ESR1、ESR2 和 PGR 的 RNA 表达检测。结果在细胞亚群之间进行量化和比较,然后使用一致流形逼近和投影(UMAP)进行可视化。通过流式细胞术对 iSGS 患者的成纤维细胞进行内分泌受体的确认性蛋白质评估(n=5)。

结果

iSGS 患者的近端气道黏膜表现出内分泌受体(ESR1、ESR2、PGR)的差异表达。在气道瘢痕中,内分泌受体主要由成纤维细胞、免疫细胞和内皮细胞表达。成纤维细胞表现出强烈的 ESR1 和 PGR 表达,而免疫细胞具有 ESR1 和 ESR2 的 RNA。内皮细胞主要表达 ESR2。无病变黏膜中的上皮细胞表达所有三种受体,而在气道瘢痕中均减少。

结论

scRNAseq 数据将内分泌受体表达定位到特定的细胞亚群。这些结果为未来研究激素依赖性机制如何促进、维持或参与 iSGS 疾病发病机制奠定了基础。

证据水平

无;基础科学喉镜,133:3506-3511,2023。

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