Department of Pediatrics, Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Mol Med. 2024 Jan 9;30(1):6. doi: 10.1186/s10020-023-00770-y.
Bronchopulmonary dysplasia (BPD) is a common chronic lung disease in preterm infants, characterised by compromised alveolar development and pulmonary vascular abnormalities. Emerging evidence suggests that regulatory T cells (Tregs) may confer protective effects on the vasculature. Knockdown of their transcription factor, interferon regulatory factor 4 (IRF4), has been shown to promote vascular endothelial hyperplasia. However, the involvement of Tregs and IRF4 in the BPD pathogenesis remains unclear. This study aimed to investigate the regulation of Tregs by IRF4 and elucidate its potential role in pulmonary vasculature development in a BPD mouse model.
The BPD model was established using 85% hyperoxia exposure, with air exposure as the normal control. Lung tissues were collected after 7 or 14 days of air or hyperoxia exposure, respectively. Haematoxylin-eosin staining was performed to assess lung tissue pathology. Immunohistochemistry was used to measure platelet endothelial cell adhesion molecule-1 (PECAM-1) level, flow cytometry to quantify Treg numbers, and Western blot to assess vascular endothelial growth factor (VEGFA), angiopoietin-1 (Ang-1), forkhead box protein P3 (FOXP3), and IRF4 protein levels. We also examined the co-expression of IRF4 and FOXP3 proteins using immunoprecipitation and immunofluorescence double staining. Furthermore, we employed CRISPR/Cas9 technology to knock down the IRF4 gene and observed changes in the aforementioned indicators to validate its effect on pulmonary vasculature development in mice.
Elevated IRF4 levels in BPD model mice led to FOXP3 downregulation, reduced Treg numbers, and impaired pulmonary vascular development. Knockdown of IRF4 resulted in improved pulmonary vascular development and upregulated FOXP3 level.
IRF4 may affect the protective role of Tregs in the proliferation of pulmonary vascular endothelial cells and pulmonary vascular development in BPD model mice by inhibiting the FOXP3 level.
支气管肺发育不良(BPD)是早产儿常见的慢性肺部疾病,其特征是肺泡发育受损和肺血管异常。新出现的证据表明调节性 T 细胞(Tregs)可能对血管具有保护作用。其转录因子干扰素调节因子 4(IRF4)的敲低已被证明可促进血管内皮细胞增生。然而,Tregs 和 IRF4 在 BPD 发病机制中的参与仍不清楚。本研究旨在研究 IRF4 对 Tregs 的调节作用,并阐明其在 BPD 小鼠模型中肺血管发育中的潜在作用。
使用 85%的高氧暴露建立 BPD 模型,空气暴露作为正常对照。分别在空气或高氧暴露 7 或 14 天后收集肺组织。进行苏木精-伊红染色以评估肺组织病理学。免疫组织化学用于测量血小板内皮细胞黏附分子-1(PECAM-1)水平,流式细胞术用于定量 Treg 数量,Western blot 用于评估血管内皮生长因子(VEGFA)、血管生成素-1(Ang-1)、叉头框蛋白 P3(FOXP3)和 IRF4 蛋白水平。我们还使用免疫沉淀和免疫荧光双重染色检查了 IRF4 和 FOXP3 蛋白的共表达。此外,我们采用 CRISPR/Cas9 技术敲低 IRF4 基因,并观察到上述指标的变化,以验证其对小鼠肺血管发育的影响。
BPD 模型小鼠中 IRF4 水平升高导致 FOXP3 下调、Treg 数量减少和肺血管发育受损。IRF4 敲低导致肺血管发育改善和 FOXP3 水平上调。
IRF4 可能通过抑制 FOXP3 水平影响 Tregs 在 BPD 模型小鼠肺血管内皮细胞增殖和肺血管发育中的保护作用。