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解析非酒精性脂肪性肝病调控基因组的细胞类型特异性研究

Cell-Type Resolved Insights into the Cis-Regulatory Genome of NAFLD.

机构信息

Department of Biochemistry and Molecular Biology, University of Southern Denmark, DK-5230 Odense, Denmark.

出版信息

Cells. 2022 Mar 3;11(5):870. doi: 10.3390/cells11050870.

DOI:10.3390/cells11050870
PMID:35269495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8909044/
Abstract

The prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing rapidly, and unmet treatment can result in the development of hepatitis, fibrosis, and liver failure. There are difficulties involved in diagnosing NAFLD early and for this reason there are challenges involved in its treatment. Furthermore, no drugs are currently approved to alleviate complications, a fact which highlights the need for further insight into disease mechanisms. NAFLD pathogenesis is associated with complex cellular changes, including hepatocyte steatosis, immune cell infiltration, endothelial dysfunction, hepatic stellate cell activation, and epithelial ductular reaction. Many of these cellular changes are controlled by dramatic changes in gene expression orchestrated by the cis-regulatory genome and associated transcription factors. Thus, to understand disease mechanisms, we need extensive insights into the gene regulatory mechanisms associated with tissue remodeling. Mapping cis-regulatory regions genome-wide is a step towards this objective and several current and emerging technologies allow detection of accessible chromatin and specific histone modifications in enriched cell populations of the liver, as well as in single cells. Here, we discuss recent insights into the cis-regulatory genome in NAFLD both at the organ-level and in specific cell populations of the liver. Moreover, we highlight emerging technologies that enable single-cell resolved analysis of the cis-regulatory genome of the liver.

摘要

非酒精性脂肪性肝病 (NAFLD) 的患病率正在迅速上升,如果得不到治疗,可能会发展为肝炎、纤维化和肝衰竭。早期诊断 NAFLD 存在困难,因此其治疗也存在挑战。此外,目前尚无药物可缓解其并发症,这一事实突显了深入了解疾病机制的必要性。NAFLD 的发病机制与复杂的细胞变化有关,包括肝细胞脂肪变性、免疫细胞浸润、内皮功能障碍、肝星状细胞激活和上皮小管反应。这些细胞变化中的许多都受到顺式调控基因组和相关转录因子协调的基因表达的剧烈变化的控制。因此,要了解疾病机制,我们需要深入了解与组织重塑相关的基因调控机制。全基因组范围内绘制顺式调控区是实现这一目标的一步,目前有几种技术和新兴技术可以检测富含肝脏细胞群以及单细胞中的可及染色质和特定组蛋白修饰。在这里,我们讨论了在器官水平和肝脏特定细胞群中,NAFLD 顺式调控基因组的最新研究进展。此外,我们还强调了新兴技术,这些技术使我们能够对肝脏的顺式调控基因组进行单细胞分辨率的分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/10b402023d5f/cells-11-00870-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/fad7894b7ddc/cells-11-00870-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/343219059a78/cells-11-00870-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/10b402023d5f/cells-11-00870-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/fad7894b7ddc/cells-11-00870-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/343219059a78/cells-11-00870-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70bc/8909044/10b402023d5f/cells-11-00870-g003.jpg

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