• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

miRNA 对 BDNF 的调控:证据更新。

BDNF Modulation by microRNAs: An Update on the Evidence.

机构信息

Department of Restorative Dentistry, Araraquara School of Dentistry, São Paulo State University (UNESP), Araraquara 14801-385, SP, Brazil.

Department of Physiology and Biochemistry, Wroclaw University of Health and Sport Sciences, 51-612 Wrocław, Poland.

出版信息

Cells. 2024 May 20;13(10):880. doi: 10.3390/cells13100880.

DOI:10.3390/cells13100880
PMID:38786102
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11119608/
Abstract

MicroRNAs can interfere with protein function by suppressing their messenger RNA translation or the synthesis of its related factors. The function of brain-derived neurotrophic factor (BDNF) is essential to the proper formation and function of the nervous system and is seen to be regulated by many microRNAs. However, understanding how microRNAs influence BDNF actions within cells requires a wider comprehension of their integrative regulatory mechanisms. : In this literature review, we have synthesized the evidence of microRNA regulation on BDNF in cells and tissues, and provided an analytical discussion about direct and indirect mechanisms that appeared to be involved in BDNF regulation by microRNAs. : Searches were conducted on PubMed.gov using the terms "BDNF" AND "MicroRNA" and "brain-derived neurotrophic factor" AND "MicroRNA", updated on 1 September 2023. Papers without open access were requested from the authors. One hundred and seventy-one papers were included for review and discussion. Results and : The local regulation of BDNF by microRNAs involves a complex interaction between a series of microRNAs with target proteins that can either inhibit or enhance BDNF expression, at the core of cell metabolism. Therefore, understanding this homeostatic balance provides resources for the future development of vector-delivery-based therapies for the neuroprotective effects of BDNF.

摘要

微小 RNA 可以通过抑制其信使 RNA 翻译或相关因子的合成来干扰蛋白质功能。脑源性神经营养因子 (BDNF) 的功能对神经系统的正常形成和功能至关重要,并且被认为受到许多微小 RNA 的调节。然而,要了解微小 RNA 如何在细胞内影响 BDNF 的作用,需要更广泛地理解它们的综合调节机制。在这篇文献综述中,我们综合了微小 RNA 对细胞和组织中 BDNF 的调节作用的证据,并对直接和间接机制进行了分析讨论,这些机制似乎参与了微小 RNA 对 BDNF 的调节。在 PubMed.gov 上使用术语“BDNF”和“微小 RNA”以及“脑源性神经营养因子”和“微小 RNA”进行了搜索,并于 2023 年 9 月 1 日进行了更新。向作者请求了没有开放获取的论文。共纳入 171 篇论文进行综述和讨论。结果和讨论微小 RNA 对 BDNF 的局部调节涉及一系列微小 RNA 与靶蛋白之间的复杂相互作用,这些微小 RNA 可以抑制或增强 BDNF 的表达,这是细胞代谢的核心。因此,了解这种体内平衡为未来基于载体传递的 BDNF 神经保护作用的治疗方法的发展提供了资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff0/11119608/aa1d4a10ea7b/cells-13-00880-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff0/11119608/d5c6acfcbf31/cells-13-00880-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff0/11119608/aa1d4a10ea7b/cells-13-00880-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff0/11119608/d5c6acfcbf31/cells-13-00880-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ff0/11119608/aa1d4a10ea7b/cells-13-00880-g002.jpg

相似文献

1
BDNF Modulation by microRNAs: An Update on the Evidence.miRNA 对 BDNF 的调控:证据更新。
Cells. 2024 May 20;13(10):880. doi: 10.3390/cells13100880.
2
A MicroRNA-BDNF Negative Feedback Signaling Loop in Brain: Implications for Alzheimer's Disease.大脑中的一个微小RNA-脑源性神经营养因子负反馈信号回路:对阿尔茨海默病的影响
Microrna. 2015;4(2):101-8. doi: 10.2174/2211536604666150813152620.
3
MicroRNA-322 Cluster Promotes Tau Phosphorylation via Targeting Brain-Derived Neurotrophic Factor.miRNA-322 簇通过靶向脑源性神经营养因子促进 Tau 磷酸化。
Neurochem Res. 2018 Mar;43(3):736-744. doi: 10.1007/s11064-018-2475-1. Epub 2018 Feb 20.
4
Dexmedetomidine had neuroprotective effects on hippocampal neuronal cells via targeting lncRNA SHNG16 mediated microRNA-10b-5p/BDNF axis.右美托咪定通过靶向 lncRNA SHNG16 介导的 microRNA-10b-5p/BDNF 轴对海马神经元细胞发挥神经保护作用。
Mol Cell Biochem. 2020 Jun;469(1-2):41-51. doi: 10.1007/s11010-020-03726-6. Epub 2020 Apr 22.
5
Regulation of Schwann cell proliferation and migration by miR-1 targeting brain-derived neurotrophic factor after peripheral nerve injury.miR-1 靶向脑源性神经营养因子调控周围神经损伤后许旺细胞的增殖和迁移。
Sci Rep. 2016 Jul 6;6:29121. doi: 10.1038/srep29121.
6
Transcript specificity in BDNF-regulated protein synthesis.BDNF 调节的蛋白质合成中的转录特异性。
Neuropharmacology. 2014 Jan;76 Pt C(0 0):657-63. doi: 10.1016/j.neuropharm.2013.05.004. Epub 2013 May 22.
7
Differential expression of microRNAs in TM3 Leydig cells of mice treated with brain-derived neurotrophic factor.脑源性神经营养因子处理的小鼠TM3睾丸间质细胞中微小RNA的差异表达
Cell Biochem Funct. 2017 Oct;35(7):364-371. doi: 10.1002/cbf.3283. Epub 2017 Oct 2.
8
Novel BDNF-regulatory microRNAs in neurodegenerative disorders pathogenesis: An in silico study.新型 BDNF 调节 microRNAs 在神经退行性疾病发病机制中的作用:一项计算机研究。
Comput Biol Chem. 2019 Dec;83:107153. doi: 10.1016/j.compbiolchem.2019.107153. Epub 2019 Nov 2.
9
MicroRNA-103 suppresses glioma cell proliferation and invasion by targeting the brain-derived neurotrophic factor.微小 RNA-103 通过靶向脑源性神经营养因子抑制神经胶质瘤细胞的增殖和侵袭。
Mol Med Rep. 2018 Mar;17(3):4083-4089. doi: 10.3892/mmr.2017.8282. Epub 2017 Dec 15.
10
Glucocorticoid attenuates brain-derived neurotrophic factor-dependent upregulation of glutamate receptors via the suppression of microRNA-132 expression.糖皮质激素通过抑制 microRNA-132 的表达来减弱脑源性神经营养因子依赖性的谷氨酸受体上调。
Neuroscience. 2010 Feb 17;165(4):1301-11. doi: 10.1016/j.neuroscience.2009.11.057. Epub 2009 Dec 1.

引用本文的文献

1
Combined Effects of Metformin, Quercetin, and Fractionated Gamma Irradiation on MiR-107-Mediated Brain Injury in HFD/STZ-Induced Diabetic Rats.二甲双胍、槲皮素和分次伽马辐射对高脂饮食/链脲佐菌素诱导的糖尿病大鼠中miR-107介导的脑损伤的联合作用
Dose Response. 2025 Aug 11;23(3):15593258251367627. doi: 10.1177/15593258251367627. eCollection 2025 Jul-Sep.
2
BDNF/proBDNF Interplay in the Mediation of Neuronal Apoptotic Mechanisms in Neurodegenerative Diseases.脑源性神经营养因子/前体脑源性神经营养因子在神经退行性疾病神经元凋亡机制介导中的相互作用
Int J Mol Sci. 2025 May 21;26(10):4926. doi: 10.3390/ijms26104926.
3
Structural and functional changes in the hippocampus induced by environmental exposures.

本文引用的文献

1
Clinical Insights into MicroRNAs in Depression: Bridging Molecular Discoveries and Therapeutic Potential.抑郁症中 microRNAs 的临床观察:弥合分子发现与治疗潜能。
Int J Mol Sci. 2024 Mar 1;25(5):2866. doi: 10.3390/ijms25052866.
2
Non-coding RNAs and neuroinflammation: implications for neurological disorders.非编码RNA与神经炎症:对神经系统疾病的影响
Exp Biol Med (Maywood). 2024 Feb 28;249:10120. doi: 10.3389/ebm.2024.10120. eCollection 2024.
3
Role and regulatory mechanism of microRNA mediated neuroinflammation in neuronal system diseases.
环境暴露引起的海马体结构和功能变化。
Neurosciences (Riyadh). 2025 Jan;30(1):5-19. doi: 10.17712/nsj.2025.1.20240052.
微小 RNA 介导的神经炎症在神经元系统疾病中的作用和调控机制。
Front Immunol. 2023 Aug 11;14:1238930. doi: 10.3389/fimmu.2023.1238930. eCollection 2023.
4
MeCP2 Is an Epigenetic Factor That Links DNA Methylation with Brain Metabolism.MeCP2 是一种将 DNA 甲基化与大脑代谢联系起来的表观遗传因子。
Int J Mol Sci. 2023 Feb 20;24(4):4218. doi: 10.3390/ijms24044218.
5
The Val66Met Polymorphism is a Relevant, But not Determinant, Risk Factor in the Etiology of Neuropsychiatric Disorders - Current Advances in Human Studies: A Systematic Review.缬氨酸66蛋氨酸多态性是神经精神疾病病因学中的一个相关但非决定性的危险因素——人类研究的当前进展:一项系统综述。
Brain Plast. 2022 Dec 20;8(2):133-142. doi: 10.3233/BPL-210132. eCollection 2022.
6
Untranslated regions of brain-derived neurotrophic factor mRNA control its translatability and subcellular localization.脑源性神经营养因子 mRNA 的未翻译区控制其翻译能力和亚细胞定位。
J Biol Chem. 2023 Feb;299(2):102897. doi: 10.1016/j.jbc.2023.102897. Epub 2023 Jan 11.
7
Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours.原肌球蛋白受体激酶 B(TrkB)信号:神经源性肿瘤的靶向治疗。
J Pathol Clin Res. 2023 Mar;9(2):89-99. doi: 10.1002/cjp2.307. Epub 2022 Dec 19.
8
Assessing the expression of two post-transcriptional BDNF regulators, TTP and miR-16 in the peripheral blood of patients with Schizophrenia.评估精神分裂症患者外周血中两个转录后 BDNF 调节剂(TTP 和 miR-16)的表达。
BMC Psychiatry. 2022 Dec 8;22(1):771. doi: 10.1186/s12888-022-04442-9.
9
A key role of miR-132-5p in the prefrontal cortex for persistent prophylactic actions of (R)-ketamine in mice.miR-132-5p 在前额叶皮层中对(R)-氯胺酮在小鼠中持续预防作用的关键作用。
Transl Psychiatry. 2022 Sep 28;12(1):417. doi: 10.1038/s41398-022-02192-6.
10
Dexmedetomidine pretreatment alleviates ropivacaine-induced neurotoxicity via the miR-10b-5p/BDNF axis.右美托咪定预处理通过 miR-10b-5p/BDNF 轴减轻罗哌卡因诱导的神经毒性。
BMC Anesthesiol. 2022 Sep 26;22(1):304. doi: 10.1186/s12871-022-01810-6.