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富含多不饱和脂肪酸的刺激的鼠巨噬细胞和人内皮细胞系的转录组和 miRNA 数据。

Transcriptom and miRNA data of PUFA-enriched stimulated murine macrophage and human endothelial cell lines.

机构信息

University Clinic and Outpatient Clinic for Anaesthesiology and Operative Intensive Care, University Medicine Halle (Saale), 06112, Halle (Saale), Germany.

出版信息

Sci Data. 2023 Jun 10;10(1):375. doi: 10.1038/s41597-023-02288-8.

Abstract

Inflammation is associated with the adaptation of macrophages and endothelial cells, and the dysregulation of these differentiation processes has been directly linked to both acute and chronic disease states. As cells in constant contact with blood, macrophages and endothelial cells are also under the direct influence of immunomodulatory dietary components such as polyunsaturated fatty acids (PUFA). RNA sequencing analyses allow us to understand the global changes in gene expression occurring during cell differentiation, including both transcriptional (transcriptome) and post-transcriptional (miRNAs) levels. We generated a comprehensive RNA sequencing dataset of parallel transcriptome and miRNA profiles of PUFA-enriched and pro-inflammatory stimulated macrophages and endothelial cells aiming to uncover the underlying molecular mechanisms. PUFA concentrations and duration of supplementation were based on dietary ranges, allowing for metabolism and plasma membrane uptake of fatty acids. The dataset may serve as a resource to study transcriptional and post-transcriptional changes associated with macrophage polarisation and endothelial dysfunction in inflammatory settings and their modulation by omega-3 and omega-6 fatty acids.

摘要

炎症与巨噬细胞和内皮细胞的适应有关,这些分化过程的失调与急性和慢性疾病状态直接相关。作为与血液持续接触的细胞,巨噬细胞和内皮细胞也受到免疫调节膳食成分(如多不饱和脂肪酸(PUFA))的直接影响。RNA 测序分析使我们能够了解细胞分化过程中发生的基因表达的全局变化,包括转录(转录组)和转录后(miRNA)水平。我们生成了一个综合的 RNA 测序数据集,包括富含多不饱和脂肪酸和促炎刺激的巨噬细胞和内皮细胞的平行转录组和 miRNA 图谱,旨在揭示潜在的分子机制。PUFA 浓度和补充时间基于饮食范围,允许脂肪酸的代谢和质膜摄取。该数据集可作为研究与炎症环境中巨噬细胞极化和内皮功能障碍相关的转录和转录后变化及其由 omega-3 和 omega-6 脂肪酸调节的资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d162/10257660/8aaf680a641c/41597_2023_2288_Fig1_HTML.jpg

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