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肺泡Ⅱ型上皮细胞纯化后 microRNA 的表达谱。

microRNA Expression Profile of Purified Alveolar Epithelial Type II Cells.

机构信息

Institute for Lung Biology and Disease, Ludwig-Maximilians University Hospital Munich, Asklepios Clinic Gauting and Helmholtz Zentrum München, Comprehensive Pneumology Center Munich, Max-Lebsche-Platz 31, 81377 Munich, Germany.

Helmholtz Zentrum München, Department Strategy, Programs, Resources, Helmholtz Zentrum München German Research Center for Environmental Health, Ingolstädter Landstraße 1, 85764 Neuherberg, Germany.

出版信息

Genes (Basel). 2022 Aug 10;13(8):1420. doi: 10.3390/genes13081420.

Abstract

Alveolar type II (ATII) cells are essential for the maintenance of the alveolar homeostasis. However, knowledge of the expression of the miRNAs and miRNA-regulated networks which control homeostasis and coordinate diverse functions of murine ATII cells is limited. Therefore, we asked how miRNAs expressed in ATII cells might contribute to the regulation of signaling pathways. We purified "untouched by antibodies" ATII cells using a flow cytometric sorting method with a highly autofluorescent population of lung cells. TaqMan miRNA low-density arrays were performed on sorted cells and intersected with miRNA profiles of ATII cells isolated according to a previously published protocol. Of 293 miRNAs expressed in both ATII preparations, 111 showed equal abundances. The target mRNAs of bona fide ATII miRNAs were used for pathway enrichment analysis. This analysis identified nine signaling pathways with known functions in fibrosis and/or epithelial-to-mesenchymal transition (EMT). In particular, a subset of 19 miRNAs was found to target 21 components of the TGF-β signaling pathway. Three of these miRNAs (miR-16-5p, -17-5p and -30c-5p) were down-modulated by TGF-β1 stimulation in human A549 cells, and concomitant up-regulation of associated mRNA targets (BMPR2, JUN, RUNX2) was observed. These results suggest an important role for miRNAs in maintaining the homeostasis of the TGF-β signaling pathway in ATII cells under physiological conditions.

摘要

肺泡 II 型 (ATII) 细胞对于维持肺泡内环境稳定至关重要。然而,控制内环境稳定和协调鼠类 ATII 细胞多种功能的 miRNA 及其调控网络的表达情况知之甚少。因此,我们想知道 ATII 细胞中表达的 miRNA 如何参与调控信号通路。我们使用一种带有高度自发荧光的肺细胞流式细胞分选方法,对“未被抗体触及”的 ATII 细胞进行纯化。对分选细胞进行 TaqMan miRNA 低密度芯片分析,并与根据先前发表的方案分离的 ATII 细胞的 miRNA 图谱进行交集。在这两种 ATII 细胞制备物中表达的 293 种 miRNA 中,有 111 种的丰度相等。真 ATII miRNA 的靶 mRNA 用于通路富集分析。该分析确定了纤维化和/或上皮间质转化 (EMT) 中具有已知功能的九条信号通路。特别是,发现一组 19 种 miRNA 可靶向 TGF-β 信号通路的 21 个成分。这三种 miRNA(miR-16-5p、-17-5p 和 -30c-5p)在人 A549 细胞中受到 TGF-β1 刺激的下调,同时观察到相关 mRNA 靶标的上调(BMPR2、JUN、RUNX2)。这些结果表明 miRNA 在维持生理条件下 ATII 细胞 TGF-β 信号通路内环境稳定方面发挥着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2ce/9407429/89a424eebb6a/genes-13-01420-g001.jpg

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