Pathophysiological Significance of Neutrophilic Transfer RNA-Derived Small RNAs in Asymptomatic Moyamoya Disease

被引:7
作者
Li, Lingzhi [1 ]
Liu, Ping [1 ]
Wang, Rongliang [1 ,2 ]
Huang, Yuyou [1 ]
Luo, Jichang [3 ]
Jiao, Liqun [3 ]
Tao, Zhen [1 ,2 ]
Zheng, Yangmin [1 ]
Fan, Junfen [1 ,2 ]
Zhao, Haiping [1 ,2 ]
Han, Ziping [1 ]
Luo, Yumin [1 ,2 ,4 ]
机构
[1] Capital Med Univ, Dept Neurol, Inst Cerebrovasc Dis Res, Xuanwu Hosp, Beijing 100000, Peoples R China
[2] Beijing Key Lab Translat Med Cerebrovasc Dis, Beijing 100000, Peoples R China
[3] Capital Med Univ, Xuanwu Hosp, Dept Neurosurg, Beijing 100000, Peoples R China
[4] Beijing Inst Brain Disorders, Beijing 100000, Peoples R China
基金
中国国家自然科学基金;
关键词
asymptomatic moyamoya disease; inflammation; neutrophil; next-generation RNA sequencing; transfer RNA-derived small RNA; BRAIN; DAMAGE;
D O I
10.3390/cells10051086
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Understanding asymptomatic moyamoya disease (aMMD), for which treatment options are currently limited, is key to the development of therapeutic strategies that will slow down the progression of this disease, as well as facilitate the discovery of therapeutic targets for symptomatic MMD. Newly found transfer RNA-derived small RNAs (tsRNAs) perform potential regulatory functions in neovascularization, which is a well-known pathological manifestation of MMD. In this study, the neutrophilic tsRNA transcriptome in aMMD was profiled using next-generation RNA sequencing in five patients and five matched healthy subjects. A negative binominal generalized log-linear regression was used to identify differentially expressed (DE)-tsRNAs in aMMD. Gene Ontology and functional pathway analyses were used to identify biological pathways involved with the targeted genes of the DE-tsRNAs. Four tsRNAs were selected and validated using quantitative reverse transcription polymerase chain reaction. In total, 186 tsRNAs were DE between the two groups. Pathophysiological events, including immune response, angiogenesis, axon guidance, and metabolism adjustment, were enriched for the DE-tsRNAs. The expression levels of the four DE-tsRNAs were consistent with those in the neutrophilic transcriptome. These aberrantly expressed tsRNAs and their targeted pathophysiological processes provide a basis for potential future interventions for aMMD.
引用
收藏
页数:11
相关论文
共 29 条
[1]   Hypoxia-Induced Degenerative Protein Modifications Associated with Aging and Age-Associated Disorders [J].
Adav, Sunil S. ;
Sze, Siu Kwan .
AGING AND DISEASE, 2020, 11 (02) :341-364
[2]   Incidence, Prevalence, and Survival of Moyamoya Disease in Korea A Nationwide, Population-Based Study [J].
Ahn, Il Min ;
Park, Dong-Hyuk ;
Hann, Hoo Jae ;
Kim, Kyoung Hoon ;
Kim, Hyun Jung ;
Ahn, Hyeong Sik .
STROKE, 2014, 45 (04) :1090-1095
[3]   The Pathophysiology of Moyamoya Disease: An Update [J].
Bang, Oh Young ;
Fujimura, Miki ;
Kim, Seung-Ki .
JOURNAL OF STROKE, 2016, 18 (01) :12-20
[4]   Epidemiology of Moyamoya Disease in China: Single-Center, Population-Based Study [J].
Bao, Xiang-Yang ;
Wang, Qian-Nan ;
Zhang, Yong ;
Zhang, Qian ;
Li, De-Sheng ;
Yang, Wei-Zhong ;
Zhang, Zheng-Shan ;
Zong, Rui ;
Han, Cong ;
Duan, Lian .
WORLD NEUROSURGERY, 2019, 122 :E917-E923
[5]   Filtering of deep sequencing data reveals the existence of abundant Dicer-dependent small RNAs derived from tRNAs [J].
Cole, Christian ;
Sobala, Andrew ;
Lu, Cheng ;
Thatcher, Shawn R. ;
Bowman, Andrew ;
Brown, John W. S. ;
Green, Pamela J. ;
Barton, Geoffrey J. ;
Hutvagner, Gyorgy .
RNA, 2009, 15 (12) :2147-2160
[6]   tiRNAs as a novel biomarker for cell damage assessment in in vitro ischemia-reperfusion model in rat neuronal PC12 cells [J].
Elkordy, Alaa ;
Rashad, Sherif ;
Shehabeldeen, Heba ;
Mishima, Eikan ;
Niizuma, Kuniyasu ;
Abe, Takaaki ;
Tominaga, Teiji .
BRAIN RESEARCH, 2019, 1714 :8-17
[7]   Increased serum production of soluble CD163 and CXCL5 in patients with moyamoya disease: Involvement of intrinsic immune reaction in its pathogenesis [J].
Fujimura, Miki ;
Fujimura, Taku ;
Kakizaki, Aya ;
Sato-Maeda, Mika ;
Niizuma, Kuniyasu ;
Tomata, Yasutake ;
Aiba, Setsuya ;
Tominaga, Teiji .
BRAIN RESEARCH, 2018, 1679 :39-44
[8]   Metabolic Adjustments by LncRNAs in Peripheral Neutrophils Partly Account for the Complete Compensation of Asymptomatic MMD Patients [J].
Han, Ziping ;
Li, Lingzhi ;
Liu, Ping ;
Huang, Yuyou ;
Zhang, Sijia ;
Li, Guangwen ;
Li, Fangfang ;
Zhao, Haiping ;
Tao, Zhen ;
Wang, Rongliang ;
Ma, Qingfeng ;
Luo, Yumin .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2020, 19 (04) :306-317
[9]   Microstructural Damage in Normal-Appearing Brain Parenchyma and Neurocognitive Dysfunction in Adult Moyamoya Disease [J].
Hara, Shoko ;
Hori, Masaaki ;
Murata, Syo ;
Ueda, Ryo ;
Tanaka, Yoji ;
Inaji, Motoki ;
Maehara, Taketoshi ;
Aoki, Shigeki ;
Nariai, Tadashi .
STROKE, 2018, 49 (10) :2504-2507
[10]   Correlation between focal brain metabolism and higher brain function in patients with Moyamoya disease [J].
Hosoda, Chihiro ;
Nariai, Tadashi ;
Ishiwata, Kiichi ;
Ishii, Kenji ;
Matsushima, Yoshiharu ;
Ohno, Kikuo .
INTERNATIONAL JOURNAL OF STROKE, 2010, 5 (05) :367-373