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衰老小鼠嗅球中 mRNAs 和长链非编码 RNA 的表达谱分析。

Expression Profiling of mRNAs and Long Non-Coding RNAs in Aged Mouse Olfactory Bulb.

机构信息

Department of Otolaryngology, Head and Neck Surgery, Beijing TongRen Hospital, Capital Medical University, Beijing, 100730, China.

Beijing Key Laboratory of Nasal Diseases, Beijing Institute of Otolaryngology, Beijing, 100005, China.

出版信息

Sci Rep. 2017 May 18;7(1):2079. doi: 10.1038/s41598-017-02329-4.

Abstract

Age-related decline in olfactory function affects the quality of life in elderly people and also potentially represents an early clinical symptom of neurodegenerative disorder. Olfactory bulb (OB) plays a central role in olfactory information transmitting and signal processing. The mechanisms underlying this impairment remain unclear. In the current study, microarray was used to investigate differentially expressed protein coding genes (PCGs) and long non-coding RNAs (lncRNAs) in OBs from three groups of mice of different ages (2 months-old young adults, 6 months-old mature adults and 20 months-old aged adults), for their potential roles in olfactory impairment. Gene Ontology and pathway analysis results showed that the differentially expressed PCGs in the OBs from aged mice were mainly associated with signal transduction, regulation of gene expression and cellular microenvironment. Similarly, gene set enrichment analysis identified two differentially and inversely expressed lncRNAs (NONMMUT004524 and NONMMUT000384), both of which were significantly associated with neuroactive ligand-receptor interaction pathway in the OBs of aged mice. These findings suggest that a decline of olfactory function in aged mice may be linked to differential expression of specific lncRNAs and their potentially adverse effects on the neuroactive ligand-receptor interaction pathway in the OB.

摘要

年龄相关的嗅觉功能下降影响老年人的生活质量,也可能代表神经退行性疾病的早期临床症状。嗅球(OB)在嗅觉信息传递和信号处理中起核心作用。其损伤的机制尚不清楚。在本研究中,我们使用微阵列技术研究了来自三组不同年龄(2 个月大的年轻人、6 个月大的成年人和 20 个月大的老年人)小鼠的 OB 中差异表达的蛋白编码基因(PCGs)和长非编码 RNA(lncRNAs),以探讨它们在嗅觉损伤中的潜在作用。GO 和通路分析结果表明,老年小鼠 OB 中差异表达的 PCGs 主要与信号转导、基因表达调控和细胞微环境有关。同样,基因集富集分析鉴定了两个差异和反向表达的 lncRNAs(NONMMUT004524 和 NONMMUT000384),它们在老年小鼠 OB 中均与神经活性配体-受体相互作用通路显著相关。这些发现表明,老年小鼠嗅觉功能下降可能与特定 lncRNAs 的差异表达及其对 OB 中神经活性配体-受体相互作用通路的潜在不利影响有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f76/5437011/684554d2a58a/41598_2017_2329_Fig1_HTML.jpg

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