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非实质细胞在肝纤维化过程中的相互作用(综述)。

Interaction of non‑parenchymal hepatocytes in the process of hepatic fibrosis (Review).

机构信息

Medical College, China Three Gorges University, Yichang, Hubei 443002, P.R. China.

The Yiling Hospital of Yichang, Yichang, Hubei 443100, P.R. China.

出版信息

Mol Med Rep. 2021 May;23(5). doi: 10.3892/mmr.2021.12003. Epub 2021 Mar 24.


DOI:10.3892/mmr.2021.12003
PMID:33760176
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7986015/
Abstract

Hepatic fibrosis (HF) is the process of fibrous scar formation caused by chronic liver injury of different etiologies. Previous studies have hypothesized that the activation of hepatic stellate cells (HSCs) is the central process in HF. The interaction between HSCs and surrounding cells is also crucial. Additionally, hepatic sinusoids capillarization, inflammation, angiogenesis and fibrosis develop during HF. The process involves multiple cell types that are highly connected and work in unison to maintain the homeostasis of the hepatic microenvironment, which serves a key role in the initiation and progression of HF. The current review provides novel insight into the intercellular interaction among liver sinusoidal endothelial cells, HSCs and Kupffer cells, as well as the hepatic microenvironment in the development of HF.

摘要

肝纤维化(HF)是由不同病因引起的慢性肝损伤导致的纤维瘢痕形成过程。既往研究假设肝星状细胞(HSCs)的激活是 HF 的核心过程。HSCs 与周围细胞的相互作用也至关重要。此外,HF 期间还会发生肝窦毛细血管化、炎症、血管生成和纤维化。该过程涉及多种细胞类型,它们高度连接并协同工作,以维持肝微环境的稳态,这在 HF 的发生和进展中起着关键作用。本综述提供了关于肝窦内皮细胞、HSCs 和枯否细胞之间的细胞间相互作用以及肝微环境在 HF 发展中的新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/87447b13a213/mmr-23-05-12003-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/41a16d715268/mmr-23-05-12003-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/dfdbcbada1ce/mmr-23-05-12003-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/79a8ca7abce5/mmr-23-05-12003-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/87447b13a213/mmr-23-05-12003-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/41a16d715268/mmr-23-05-12003-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/dfdbcbada1ce/mmr-23-05-12003-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/79a8ca7abce5/mmr-23-05-12003-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae19/7986015/87447b13a213/mmr-23-05-12003-g03.jpg

相似文献

[1]
Interaction of non‑parenchymal hepatocytes in the process of hepatic fibrosis (Review).

Mol Med Rep. 2021-5

[2]
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[3]
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[4]
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[7]
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[8]
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[9]
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[10]
[Research progress of liver sinusoidal endothelial cells in the regulation of liver microenvironment to affect liver fibrosis].

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[1]
Defenestration of Liver Sinusoidal Endothelial Cells: The Trigger of Liver Fibrosis.

Pharmaceuticals (Basel). 2025-6-14

[2]
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J Cell Mol Med. 2025-6

[3]
The potential roles of gut microbiome in porto-sinusoidal vascular disease: an under-researched crossroad.

Front Microbiol. 2025-3-3

[4]
The role of ferroptosis-related non-coding RNA in liver fibrosis.

Front Cell Dev Biol. 2024-12-9

[5]
Liver sinusoidal endothelial cell: An important yet often overlooked player in the liver fibrosis.

Clin Mol Hepatol. 2024-7

[6]
Role of Perturbated Hemostasis in MASLD and Its Correlation with Adipokines.

Life (Basel). 2024-1-7

[7]
Coagulation Dysfunctions in Non-Alcoholic Fatty Liver Disease-Oxidative Stress and Inflammation Relevance.

Medicina (Kaunas). 2023-9-7

[8]
Liver Ultrasound Histotripsy: Novel Analysis of the Histotripsy Site Cell Constituents with Implications for Histotripsy Application in Cell Transplantation and Cancer Therapy.

Bioengineering (Basel). 2023-2-20

[9]
Biodistribution Profile of Magnetic Nanoparticles in Cirrhosis-Associated Hepatocarcinogenesis in Rats by AC Biosusceptometry.

Pharmaceutics. 2022-9-8

[10]
The Role of Macrophages in Liver Fibrosis: New Therapeutic Opportunities.

Int J Mol Sci. 2022-6-14

本文引用的文献

[1]
The Endothelium as a Driver of Liver Fibrosis and Regeneration.

Cells. 2020-4-10

[2]
Intercellular crosstalk of hepatic stellate cells in liver fibrosis: New insights into therapy.

Pharmacol Res. 2020-5

[3]
Macrophage Phenotype and Function in Liver Disorder.

Front Immunol. 2020-1-28

[4]
Does Mechanocrine Signaling by Liver Sinusoidal Endothelial Cells Offer New Opportunities for the Development of Anti-fibrotics?

Front Med (Lausanne). 2020-1-9

[5]
Interplay Between Macrophages and Angiogenesis: A Double-Edged Sword in Liver Disease.

Front Immunol. 2019-12-12

[6]
Hypoxia induces the activation of hepatic stellate cells through the PVT1-miR-152-ATG14 signaling pathway.

Mol Cell Biochem. 2019-12-21

[7]
Fuzhenghuayu Decoction ameliorates hepatic fibrosis by attenuating experimental sinusoidal capillarization and liver angiogenesis.

Sci Rep. 2019-12-10

[8]
Vascular Targets for the Treatment of Portal Hypertension.

Semin Liver Dis. 2019-7-17

[9]
Bone Morphogenetic Protein 9 Is a Paracrine Factor Controlling Liver Sinusoidal Endothelial Cell Fenestration and Protecting Against Hepatic Fibrosis.

Hepatology. 2019-5-31

[10]
Hepatic microcirculation and mechanisms of portal hypertension.

Nat Rev Gastroenterol Hepatol. 2019-4

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