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miRNAs 可能参与肺移植后闭塞性细支气管炎:miR-21-5p 的作用。

miRNAs Potentially Involved in Post Lung Transplant-Obliterative Bronchiolitis: The Role of miR-21-5p.

机构信息

Research Laboratory of Lung Diseases, Section of Cell Biology, IRCCS Policlinico San Matteo Foundation, 27100 Pavia, Italy.

Department of Molecular Medicine, University of Pavia, 27100 Pavia, Italy.

出版信息

Cells. 2021 Mar 20;10(3):688. doi: 10.3390/cells10030688.

DOI:10.3390/cells10030688
PMID:33804639
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8003603/
Abstract

Epigenetic changes, including miRNAs deregulation, have been suggested to play a significant role in development of obliterative bronchiolitis (OB) in transplanted lungs. Many studies have tried to identify ideal candidate miRNAs and the downstream pathways implicated in the bronchiolar fibro-obliterative process. Several candidate miRNAs, previously indicated as possibly being associated with OB, were analyzed by combining the quantitative real time-polymerase chain reaction (qRT-PCR) and in situ hybridization (ISH) of lung tissues of OB affected patients. Disease and OB-lesion-specific expression of miR-21-5p was confirmed and by computational analysis we were able to identify the network of genes most probably associated miR-21-5p in the context of OB fibrogenesis. Among all potentially associated genes, STAT3 had a very high probability score. Immunohistochemistry showed that STAT3/miR-21-5p were co-over expressed in OB lesions, thus, suggesting miR-21-5p could regulate STAT3 expression. However, miR-21-5p inhibition in cultures of bronchiolitis obliterans syndrome (BOS) derived myofibroblasts did not significantly affect STAT3 mRNA and protein expression levels. This study demonstrates the specificity of miR-21-5p over-expression in OB lesions and contributes to existing knowledge on the miR-21-5p downstream pathway. Activation of STAT3 is associated with miR-21-5p upregulation, however, STAT-3 network activation is most likely complex and miR-21-5p is not the sole regulator of STAT3.

摘要

表观遗传改变,包括 miRNA 失调,已被认为在移植肺中的闭塞性细支气管炎 (OB) 的发展中发挥重要作用。许多研究试图确定理想的候选 miRNA 及其在细支气管纤维性闭塞过程中涉及的下游途径。通过结合定量实时聚合酶链反应 (qRT-PCR) 和 OB 受影响患者的肺组织原位杂交 (ISH),分析了先前表明可能与 OB 相关的几个候选 miRNA。确认了 miR-21-5p 的疾病和 OB 病变特异性表达,并通过计算分析,我们能够确定在 OB 纤维化背景下与 miR-21-5p 最相关的基因网络。在所有潜在相关基因中,STAT3 的概率评分非常高。免疫组织化学显示,STAT3/miR-21-5p 在 OB 病变中共同过表达,因此,提示 miR-21-5p 可能调节 STAT3 表达。然而,在源自闭塞性细支气管炎综合征 (BOS) 的肌成纤维细胞培养物中抑制 miR-21-5p 并没有显著影响 STAT3 mRNA 和蛋白表达水平。本研究证明了 miR-21-5p 在 OB 病变中的特异性过表达,并为 miR-21-5p 下游途径的现有知识做出了贡献。STAT3 的激活与 miR-21-5p 的上调相关,但是,STAT-3 网络的激活很可能是复杂的,miR-21-5p 不是 STAT3 的唯一调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/237dea127794/cells-10-00688-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/1ce580d62cac/cells-10-00688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/bfe9ca478426/cells-10-00688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/e8330c51b4b3/cells-10-00688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/e56724df35f1/cells-10-00688-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/077e227caa11/cells-10-00688-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/237dea127794/cells-10-00688-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/1ce580d62cac/cells-10-00688-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/bfe9ca478426/cells-10-00688-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/e8330c51b4b3/cells-10-00688-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/e56724df35f1/cells-10-00688-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/077e227caa11/cells-10-00688-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abd2/8003603/237dea127794/cells-10-00688-g006.jpg

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