体外庆大霉素暴露改变耳蜗螺旋韧带周细胞小泡蛋白谱。

IF 2.1 3区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Proteome Science Pub Date : 2018-03-16 eCollection Date: 2018-01-01 DOI:10.1186/s12953-018-0132-x
Elisa Ghelfi, Yohann Grondin, Emil J Millet, Adam Bartos, Magda Bortoni, Clara Oliveira Gomes Dos Santos, Humberto J Trevino-Villarreal, Rosalinda Sepulveda, Rick Rogers
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引用次数: 4

摘要

背景:氨基糖苷类抗生素庆大霉素是一种耳毒性药物,已被实验用于研究噪声引起的耳蜗损伤。我们研究了庆大霉素治疗和未治疗的螺旋韧带(SL)周细胞(内耳微血管血迷宫屏障中的特化细胞)中与小泡相关的蛋白质谱的变化。来自各种微血管床的周细胞表达小泡、富含蛋白质和胆固醇的微结构域,这些微结构域可以进行内吞作用和胞吞作用,将小分子运输进出细胞。在运输专门化的小泡中,不同的蛋白质谱可能引起影响血迷宫屏障完整性的病理变化,最终导致听力损失。方法:从处理和未处理的细胞中分离小囊泡,通过不连续梯度的裂解物进行超离心。质谱(LC-MS/MS)分析鉴定了两组蛋白。然后将未经处理的SL周细胞分离的小泡蛋白与庆大霉素处理24小时的SL周细胞分离的小泡蛋白进行比较。使用生物信息学工具分析数据。结果:庆大霉素处理细胞的小窝蛋白组显示,在庆大霉素处理期间,与小窝相关的蛋白占总蛋白的40%,而在未处理的细胞中,正常与小窝相关的蛋白有15%被抑制。数据的生物信息学分析显示,庆大霉素处理细胞中参与遗传信息处理的蛋白质表达减少,而参与代谢、囊泡运输和信号转导的蛋白质表达增加。几种Rab GTPases蛋白,普遍存在的转运蛋白,独特地与小泡分离,并在庆大霉素处理的细胞中显著富集。结论:我们报道了庆大霉素暴露改变SL周细胞小泡的蛋白谱。我们发现了一组在处理过程中独特地与小泡分离的蛋白质,主要参与代谢和生物合成途径、运输途径和遗传信息处理。最后,我们首次展示了与小窝SL周细胞相关的蛋白质与非综合征性听力损失有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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In vitro gentamicin exposure alters caveolae protein profile in cochlear spiral ligament pericytes.

Background: The aminoglycoside antibiotic gentamicin is an ototoxic drug and has been used experimentally to investigate cochlear damage induced by noise.We have investigated the changes in the protein profile associated with caveolae in gentamicin treated and untreated spiral ligament (SL) pericytes, specialized cells in the blood labyrinth barrier of the inner ear microvasculature. Pericytes from various microvascular beds express caveolae, protein and cholesterol rich microdomains, which can undergo endocytosis and transcytosis to transport small molecules in and out the cells. A different protein profile in transport-specialized caveolae may induce pathological changes affecting the integrity of the blood labyrinth barrier and ultimately contributing to hearing loss.

Method: Caveolae isolation from treated and untreated cells is achieved through ultracentrifugation of the lysates in discontinuous gradients. Mass spectrometry (LC-MS/MS) analysis identifies the proteins in the two groups. Proteins segregating with caveolae isolated from untreated SL pericytes are then compared to caveolae isolated from SL pericytes treated with the gentamicin for 24 h. Data are analyzed using bioinformatic tools.

Results: The caveolae proteome in gentamicin treated cells shows that 40% of total proteins are uniquely associated with caveolae during the treatment, and 15% of the proteins normally associated with caveolae in untreated cell are suppressed. Bioinformatic analysis of the data shows a decreased expression of proteins involved in genetic information processing, and an increase in proteins involved in metabolism, vesicular transport and signal transduction in gentamicin treated cells. Several Rab GTPases proteins, ubiquitous transporters, uniquely segregate with caveolae and are significantly enriched in gentamicin treated cells.

Conclusion: We report that gentamicin exposure modifies protein profile of caveolae from SL pericytes. We identified a pool of proteins which are uniquely segregating with caveolae during the treatment, mainly participating in metabolic and biosynthetic pathways, in transport pathways and in genetic information processing. Finally, we show for the first time proteins associated with caveolae SL pericytes linked to nonsyndromic hearing loss.

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来源期刊
Proteome Science
Proteome Science 生物-生化研究方法
CiteScore
2.90
自引率
0.00%
发文量
17
审稿时长
4.5 months
期刊介绍: Proteome Science is an open access journal publishing research in the area of systems studies. Proteome Science considers manuscripts based on all aspects of functional and structural proteomics, genomics, metabolomics, systems analysis and metabiome analysis. It encourages the submissions of studies that use large-scale or systems analysis of biomolecules in a cellular, organismal and/or environmental context. Studies that describe novel biological or clinical insights as well as methods-focused studies that describe novel methods for the large-scale study of any and all biomolecules in cells and tissues, such as mass spectrometry, protein and nucleic acid microarrays, genomics, next-generation sequencing and computational algorithms and methods are all within the scope of Proteome Science, as are electron topography, structural methods, proteogenomics, chemical proteomics, stem cell proteomics, organelle proteomics, plant and microbial proteomics. In spite of its name, Proteome Science considers all aspects of large-scale and systems studies because ultimately any mechanism that results in genomic and metabolomic changes will affect or be affected by the proteome. To reflect this intrinsic relationship of biological systems, Proteome Science will consider all such articles.
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