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作为一种替代高等生物的体内肺研究模型。

as an Alternative Model to Higher Organisms for In Vivo Lung Research.

机构信息

Division of Early Life Origins of Chronic Lung Diseases, Research Center Borstel-Leibniz Lung Center, Airway Research Center North (ARCN), German Center for Lung Research (DZL), 23845 Borstel, Germany.

Division of Molecular Physiology, Institute of Zoology, Christian-Albrechts University Kiel, Airway Research Center North (ARCN), German Center for Lung Research (DZL), 24118 Kiel, Germany.

出版信息

Int J Mol Sci. 2024 Sep 25;25(19):10324. doi: 10.3390/ijms251910324.

DOI:10.3390/ijms251910324
PMID:39408654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11476989/
Abstract

COPD and asthma are lung diseases that cause considerable burden to more than 800 million people worldwide. As both lung diseases are so far incurable, it is mandatory to understand the mechanisms underlying disease development and progression for developing novel therapeutic approaches. Exposures to environmental cues such as cigarette smoke in earliest life are known to increase disease risks in the individual's own future. To explore the pathomechanisms leading to later airway disease, mammalian models are instrumental. However, such in vivo experiments are time-consuming and burdensome for the animals, which applies in particular to transgenerational studies. Along this line, the fruit fly comes with several advantages for research in this field. The short lifespan facilitates transgenerational studies. A high number of evolutionary conserved signaling pathways, together with a large toolbox for tissue-specific gene modification, has the potential to identify novel target genes involved in disease development. A well-defined airway microbiome could help to untangle interactions between disease development and microbiome composition. In the following article, is therefore presented and discussed as an alternative in vivo model to investigate airway diseases that can complement and/or replace models in higher organisms.

摘要

COPD 和哮喘是两种肺部疾病,在全球范围内给超过 8 亿人带来了巨大的负担。由于这两种肺部疾病目前都无法治愈,因此必须了解疾病发展和进展的机制,以开发新的治疗方法。众所周知,生命早期接触香烟烟雾等环境线索会增加个体未来患疾病的风险。为了探索导致后期气道疾病的发病机制,哺乳动物模型是必不可少的。然而,此类体内实验对于动物来说既耗时又费力,特别是对于跨代研究而言。在这方面,果蝇在该领域的研究中有几个优势。其较短的寿命有利于跨代研究。大量进化上保守的信号通路,加上组织特异性基因修饰的大量工具包,有可能鉴定出参与疾病发展的新靶基因。明确的气道微生物组有助于理清疾病发展与微生物组组成之间的相互作用。因此,在接下来的文章中,果蝇被提出并讨论为一种替代的体内模型,用于研究气道疾病,可补充和/或替代高等生物中的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/9bf1016f5c2a/ijms-25-10324-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/cf79bafff357/ijms-25-10324-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/51fbdfc001b1/ijms-25-10324-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/70d7befdc0f4/ijms-25-10324-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/9bf1016f5c2a/ijms-25-10324-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/cf79bafff357/ijms-25-10324-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/51fbdfc001b1/ijms-25-10324-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/70d7befdc0f4/ijms-25-10324-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d19/11476989/9bf1016f5c2a/ijms-25-10324-g004.jpg

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Sci Rep. 2024 Jul 17;14(1):16567. doi: 10.1038/s41598-024-66752-0.
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Epigenetic inheritance of diet-induced and sperm-borne mitochondrial RNAs.饮食诱导和精子携带的线粒体 RNA 的表观遗传遗传。
Nature. 2024 Jun;630(8017):720-727. doi: 10.1038/s41586-024-07472-3. Epub 2024 Jun 5.
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Addiction. 2024 Aug;119(8):1493-1494. doi: 10.1111/add.16507. Epub 2024 Apr 23.
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Mouse Genome Informatics: an integrated knowledgebase system for the laboratory mouse.鼠类基因组信息学:用于实验鼠的综合知识库系统。
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Eur Respir J. 2024 Apr 4;63(4). doi: 10.1183/13993003.01397-2023. Print 2024 Apr.
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