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软骨形成的时间转录组特征。

The temporal transcriptomic signature of cartilage formation.

机构信息

Department of Anatomy, Histology and Embryology, Faculty of Medicine, University of Debrecen, Debrecen, H-4032, Hungary.

Genomic Medicine and Bioinformatic Core Facility, Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Debrecen, Debrecen H-4032, Hungary.

出版信息

Nucleic Acids Res. 2023 May 8;51(8):3590-3617. doi: 10.1093/nar/gkad210.

Abstract

Chondrogenesis is a multistep process, in which cartilage progenitor cells generate a tissue with distinct structural and functional properties. Although several approaches to cartilage regeneration rely on the differentiation of implanted progenitor cells, the temporal transcriptomic landscape of in vitro chondrogenesis in different models has not been reported. Using RNA sequencing, we examined differences in gene expression patterns during cartilage formation in micromass cultures of embryonic limb bud-derived progenitors. Principal component and trajectory analyses revealed a progressively different and distinct transcriptome during chondrogenesis. Differentially expressed genes (DEGs), based on pairwise comparisons of samples from consecutive days were classified into clusters and analysed. We confirmed the involvement of the top DEGs in chondrogenic differentiation using pathway analysis and identified several chondrogenesis-associated transcription factors and collagen subtypes that were not previously linked to cartilage formation. Transient gene silencing of ATOH8 or EBF1 on day 0 attenuated chondrogenesis by deregulating the expression of key osteochondrogenic marker genes in micromass cultures. These results provide detailed insight into the molecular mechanism of chondrogenesis in primary micromass cultures and present a comprehensive dataset of the temporal transcriptomic landscape of chondrogenesis, which may serve as a platform for new molecular approaches in cartilage tissue engineering.

摘要

软骨发生是一个多步骤的过程,在此过程中软骨祖细胞产生具有独特结构和功能特性的组织。尽管几种软骨再生方法依赖于植入祖细胞的分化,但不同模型中体外软骨发生的时间转录组图谱尚未报道。我们使用 RNA 测序,研究了胚胎肢芽衍生祖细胞微团培养中软骨形成过程中基因表达模式的差异。主成分和轨迹分析显示,在软骨发生过程中,转录组逐渐不同且独特。基于连续几天样本的两两比较,对差异表达基因 (DEGs) 进行分类和分析。我们使用通路分析证实了 top DEGs 在软骨分化中的参与,并鉴定了几个以前与软骨形成无关的软骨发生相关转录因子和胶原亚型。在第 0 天对 ATOH8 或 EBF1 进行瞬时基因沉默,通过调节微团培养中关键成骨软骨标记基因的表达,减弱了软骨发生。这些结果提供了对原代微团培养中软骨发生分子机制的详细了解,并提供了软骨发生时间转录组图谱的综合数据集,可作为软骨组织工程中新型分子方法的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae85/10164575/357c92b4921f/gkad210figgra1.jpg

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