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in vitro .

作者信息

Li Jiehan, Jin Christopher, Gustafsson Stefan, Rao Abhiram, Wabitsch Martin, Park Chong Y, Quertermous Thomas, Bielczyk-Maczynska Ewa, Knowles Joshua W

机构信息

Division of Cardiovascular Medicine, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.

Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, CA, 94305, USA.

出版信息

bioRxiv. 2023 Mar 29:2023.03.27.534456. doi: 10.1101/2023.03.27.534456.

Abstract

Adipogenesis is a process in which fat-specific progenitor cells (preadipocytes) differentiate into adipocytes that carry out the key metabolic functions of the adipose tissue, including glucose uptake, energy storage, and adipokine secretion. Several cell lines are routinely used to study the molecular regulation of adipogenesis, in particular the immortalized mouse 3T3-L1 line and the primary human Simpson-Golabi-Behmel syndrome (SGBS) line. However, the cell-to-cell variability of transcriptional changes prior to and during adipogenesis in these models is not well understood. Here, we present a single-cell RNA-Sequencing (scRNA-Seq) dataset collected before and during adipogenic differentiation of 3T3-L1 and SGBS cells. To minimize the effects of experimental variation, we mixed 3T3-L1 and SGBS cells and used computational analysis to demultiplex transcriptomes of mouse and human cells. In both models, adipogenesis results in the appearance of three cell clusters, corresponding to preadipocytes, early and mature adipocytes. These data provide a groundwork for comparative studies on human and mouse adipogenesis, as well as on cell-to-cell variability in gene expression during this process.

摘要

脂肪生成是一个过程,在此过程中,脂肪特异性祖细胞(前脂肪细胞)分化为脂肪细胞,这些脂肪细胞执行脂肪组织的关键代谢功能,包括葡萄糖摄取、能量储存和脂肪因子分泌。几种细胞系经常用于研究脂肪生成的分子调控,特别是永生化小鼠3T3-L1细胞系和原代人辛普森-戈拉比-贝梅尔综合征(SGBS)细胞系。然而,在这些模型中,脂肪生成之前和期间转录变化的细胞间变异性尚未得到很好的理解。在这里,我们展示了一个在3T3-L1和SGBS细胞脂肪生成分化之前和期间收集的单细胞RNA测序(scRNA-Seq)数据集。为了尽量减少实验变异的影响,我们将3T3-L1和SGBS细胞混合,并使用计算分析对小鼠和人类细胞的转录组进行解复用。在这两种模型中,脂肪生成都会导致出现三个细胞簇,分别对应前脂肪细胞、早期和成熟脂肪细胞。这些数据为人类和小鼠脂肪生成的比较研究以及该过程中基因表达的细胞间变异性研究提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/649e/10081256/913ba6c32c74/nihpp-2023.03.27.534456v1-f0001.jpg

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