Suppr超能文献

内吞途径在肝脏功能和疾病中的重要性。

Importance of endocytic pathways in liver function and disease.

作者信息

Schroeder Barbara, McNiven Mark A

机构信息

Department of Biochemistry and Molecular Biology, Center for Basic Research in Digestive Diseases, Mayo Clinic and Foundation, Rochester, Minnesota.

出版信息

Compr Physiol. 2014 Oct;4(4):1403-17. doi: 10.1002/cphy.c140001.

Abstract

Hepatocellular endocytosis is a highly dynamic process responsible for the internalization of a variety of different receptor ligand complexes, trophic factors, lipids, and, unfortunately, many different pathogens. The uptake of these external agents has profound effects on seminal cellular processes including signaling cascades, migration, growth, and proliferation. The hepatocyte, like other well-polarized epithelial cells, possesses a host of different endocytic mechanisms and entry routes to ensure the selective internalization of cargo molecules. These pathways include receptor-mediated endocytosis, lipid raft associated endocytosis, caveolae, or fluid-phase uptake, although there are likely many others. Understanding and defining the regulatory mechanisms underlying these distinct entry routes, sorting and vesicle formation, as well as the postendocytic trafficking pathways is of high importance especially in the liver, as their mis-regulation can contribute to aberrant liver pathology and liver diseases. Further, these processes can be "hijacked" by a variety of different infectious agents and viruses. This review provides an overview of common components of the endocytic and postendocytic trafficking pathways utilized by hepatocytes. It will also discuss in more detail how these general themes apply to liver-specific processes including iron homeostasis, HBV infection, and even hepatic steatosis.

摘要

肝细胞内吞作用是一个高度动态的过程,负责多种不同受体 - 配体复合物、营养因子、脂质以及不幸的是许多不同病原体的内化。这些外源物质的摄取对包括信号级联、迁移、生长和增殖在内的重要细胞过程具有深远影响。肝细胞与其他极性良好的上皮细胞一样,拥有许多不同的内吞机制和进入途径,以确保货物分子的选择性内化。这些途径包括受体介导的内吞作用、脂筏相关的内吞作用、小窝或液相摄取,尽管可能还有许多其他途径。理解和定义这些不同进入途径、分选和囊泡形成以及内吞后运输途径背后的调控机制非常重要,尤其是在肝脏中,因为它们的失调可能导致异常的肝脏病理和肝脏疾病。此外,这些过程可能会被多种不同的感染因子和病毒“劫持”。本综述概述了肝细胞利用的内吞和内吞后运输途径的常见组成部分。它还将更详细地讨论这些一般主题如何应用于肝脏特异性过程,包括铁稳态、乙肝病毒感染,甚至肝脂肪变性。

相似文献

1
Importance of endocytic pathways in liver function and disease.
Compr Physiol. 2014 Oct;4(4):1403-17. doi: 10.1002/cphy.c140001.
2
Clathrin-independent endocytosis: new insights into caveolae and non-caveolar lipid raft carriers.
Biochim Biophys Acta. 2005 Sep 30;1745(3):273-86. doi: 10.1016/j.bbamcr.2005.06.002.
3
Calcium-Sensing Receptor: Trafficking, Endocytosis, Recycling, and Importance of Interacting Proteins.
Prog Mol Biol Transl Sci. 2015;132:127-50. doi: 10.1016/bs.pmbts.2015.02.006. Epub 2015 Apr 25.
4
Secrets of caveolae- and lipid raft-mediated endocytosis revealed by mammalian viruses.
Biochim Biophys Acta. 2005 Dec 30;1746(3):295-304. doi: 10.1016/j.bbamcr.2005.06.009. Epub 2005 Jul 5.
5
Regulation of raft-dependent endocytosis.
J Cell Mol Med. 2007 Jul-Aug;11(4):644-53. doi: 10.1111/j.1582-4934.2007.00083.x.
6
Virus entry by endocytosis.
Annu Rev Biochem. 2010;79:803-33. doi: 10.1146/annurev-biochem-060208-104626.
7
Peptide-mediated protein delivery-which pathways are penetrable?
Biochim Biophys Acta. 2010 Dec;1798(12):2240-8. doi: 10.1016/j.bbamem.2010.02.013. Epub 2010 Feb 17.
8
Caveosomes and endocytosis of lipid rafts.
J Cell Sci. 2003 Dec 1;116(Pt 23):4707-14. doi: 10.1242/jcs.00840.
9
Shaping membranes for endocytosis.
Rev Physiol Biochem Pharmacol. 2011;161:45-66. doi: 10.1007/112_2008_2.
10
New insights into membrane trafficking and protein sorting.
Int Rev Cytol. 2007;261:47-116. doi: 10.1016/S0074-7696(07)61002-X.

引用本文的文献

1
Diverse actions of 15 structurally unrelated mitochondrial uncouplers in cells and mice.
Mol Metab. 2025 Jul 8;99:102204. doi: 10.1016/j.molmet.2025.102204.
4
Immunotoxins Immunotherapy against Hepatocellular Carcinoma: A Promising Prospect.
Toxins (Basel). 2021 Oct 11;13(10):719. doi: 10.3390/toxins13100719.
5
Antibody-drug conjugate as targeted therapeutics against hepatocellular carcinoma: preclinical studies and clinical relevance.
Clin Transl Oncol. 2022 Mar;24(3):407-431. doi: 10.1007/s12094-021-02707-5. Epub 2021 Sep 30.
7
Hepatitis B Virus Entry into Cells.
Cells. 2020 Jun 18;9(6):1486. doi: 10.3390/cells9061486.
8
The cell biology of the hepatocyte: A membrane trafficking machine.
J Cell Biol. 2019 Jul 1;218(7):2096-2112. doi: 10.1083/jcb.201903090. Epub 2019 Jun 14.
9
Inhibitory effect of silibinin on hepatitis B virus entry.
Biochem Biophys Rep. 2018 Mar 31;14:20-25. doi: 10.1016/j.bbrep.2018.03.003. eCollection 2018 Jul.

本文引用的文献

2
Hepatitis B and D viruses exploit sodium taurocholate co-transporting polypeptide for species-specific entry into hepatocytes.
Gastroenterology. 2014 Apr;146(4):1070-83. doi: 10.1053/j.gastro.2013.12.024. Epub 2013 Dec 19.
3
Lipid droplet breakdown requires dynamin 2 for vesiculation of autolysosomal tubules in hepatocytes.
J Cell Biol. 2013 Oct 28;203(2):315-26. doi: 10.1083/jcb.201306140. Epub 2013 Oct 21.
4
Clathrin-independent endocytosis: a cargo-centric view.
Exp Cell Res. 2013 Nov 1;319(18):2759-69. doi: 10.1016/j.yexcr.2013.08.008. Epub 2013 Aug 13.
5
Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA).
Curr Neuropharmacol. 2013 Jan;11(1):59-79. doi: 10.2174/157015913804999469.
6
Building a fission machine--structural insights into dynamin assembly and activation.
J Cell Sci. 2013 Jul 1;126(Pt 13):2773-84. doi: 10.1242/jcs.108845. Epub 2013 Jun 18.
8
Up-to-date membrane biogenesis in the autophagosome formation.
Curr Opin Cell Biol. 2013 Aug;25(4):455-60. doi: 10.1016/j.ceb.2013.03.004. Epub 2013 Apr 8.
9
Autophagosomes form at ER-mitochondria contact sites.
Nature. 2013 Mar 21;495(7441):389-93. doi: 10.1038/nature11910. Epub 2013 Mar 3.
10
β-Arrestins and G protein-coupled receptor trafficking.
Methods Enzymol. 2013;521:91-108. doi: 10.1016/B978-0-12-391862-8.00005-3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验