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慢性中耳炎培养阳性患者自噬标志物表达降低。

Decreased expression of autophagy markers in culture-positive patients with chronic otitis media.

作者信息

Jung Junyang, Park Dong Choon, Kim Young Il, Lee Eun Hye, Park Myung Jin, Kim Sang Hoon, Yeo Seung Geun

机构信息

Department of Anatomy and Neurobiology, College of Medicine, Kyung Hee University, Seoul, Korea.

St. Vincent's Hospital, The Catholic University of Korea, Suwon, Korea.

出版信息

J Int Med Res. 2020 Jun;48(6):300060520936174. doi: 10.1177/0300060520936174.

DOI:10.1177/0300060520936174
PMID:32589484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7323285/
Abstract

OBJECTIVE

Abnormal autophagy plays a role in the pathogenesis of various diseases. This study aimed to evaluate associations between the clinical manifestations of chronic otitis media (COM) and expression of autophagy markers.

METHODS

Associations between presence of bacteria, otorrhea, and conductive and sensorineural hearing loss and levels of autophagy-related mRNAs were investigated in 47 patients with COM.

RESULTS

Autophagy-related mRNAs were detected in all inflammatory tissues of COM patients. LC3-II showed the highest level of expression, followed by Beclin-1, P13KC3, Rubicon, and mTOR. Beclin-1 mRNA levels were significantly lower in culture-positive than in culture-negative patients.

CONCLUSION

Autophagy is involved in the pathogenesis of COM. The finding that expression of autophagy markers, especially Beclin-1, was lower in culture-positive than in culture-negative patients suggested that these markers are closely associated with the clinical features of COM.

摘要

目的

异常自噬在多种疾病的发病机制中起作用。本研究旨在评估慢性中耳炎(COM)的临床表现与自噬标志物表达之间的关联。

方法

在47例COM患者中,研究细菌的存在、耳漏以及传导性和感音神经性听力损失与自噬相关mRNA水平之间的关联。

结果

在COM患者的所有炎症组织中均检测到自噬相关mRNA。LC3-II表达水平最高,其次是Beclin-1、P13KC3、Rubicon和mTOR。培养阳性患者的Beclin-1 mRNA水平显著低于培养阴性患者。

结论

自噬参与COM的发病机制。培养阳性患者的自噬标志物,尤其是Beclin-1的表达低于培养阴性患者,这一发现表明这些标志物与COM的临床特征密切相关。

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本文引用的文献

1
Lower Beclin-1 mRNA Levels in Pediatric Compared With Adult Patients With Otitis Media With Effusion.与成人分泌性中耳炎患者相比,小儿患者中Beclin-1 mRNA水平较低。
J Int Adv Otol. 2018 Apr;14(1):48-52. doi: 10.5152/iao.2018.4481.
2
Expression of aquaporins mRNAs in patients with otitis media.中耳炎患者水通道蛋白mRNA的表达
Acta Otolaryngol. 2018 Aug;138(8):701-707. doi: 10.1080/00016489.2018.1447685. Epub 2018 Apr 1.
3
A Review: Expression of Aquaporins in Otitis Media.综述:耳炎中水通道蛋白的表达。
Int J Mol Sci. 2017 Oct 17;18(10):2164. doi: 10.3390/ijms18102164.
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Mitochondrial Control of Innate Immunity and Inflammation.线粒体对固有免疫和炎症的调控
Immune Netw. 2017 Apr;17(2):77-88. doi: 10.4110/in.2017.17.2.77. Epub 2017 Apr 20.
5
Rubicon swaps autophagy for LAP.鲁比孔河将自噬切换为 LAP。
Nat Cell Biol. 2015 Jul;17(7):843-5. doi: 10.1038/ncb3197.
6
Autophagy in autoimmune disease.自身免疫性疾病中的自噬
J Mol Med (Berl). 2015 Jul;93(7):707-17. doi: 10.1007/s00109-015-1297-8. Epub 2015 Jun 10.
7
Essential role for autophagy in life span extension.自噬在寿命延长中起关键作用。
J Clin Invest. 2015 Jan;125(1):85-93. doi: 10.1172/JCI73946. Epub 2015 Jan 2.
8
mTOR: a pharmacologic target for autophagy regulation.mTOR:自噬调节的药理学靶点。
J Clin Invest. 2015 Jan;125(1):25-32. doi: 10.1172/JCI73939. Epub 2015 Jan 2.
9
Role of innate immunity in the pathogenesis of otitis media.天然免疫在中耳炎发病机制中的作用。
Int J Infect Dis. 2014 Dec;29:259-67. doi: 10.1016/j.ijid.2014.10.015. Epub 2014 Nov 5.
10
Autosis and autophagic cell death: the dark side of autophagy.自噬性细胞死亡与自噬性细胞凋亡:自噬的阴暗面
Cell Death Differ. 2015 Mar;22(3):367-76. doi: 10.1038/cdd.2014.143. Epub 2014 Sep 26.