» Articles » PMID: 30469540

Liver-Derived Exosomes and Their Implications in Liver Pathobiology

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2018 Nov 25
PMID 30469540
Citations 43
Authors
Affiliations
Soon will be listed here.
Abstract

The liver has a wide range of physiological functions in the body, and its health is maintained by complex cross-talk among hepatic cells, including parenchymal hepatocytes and nonparenchymal cells. Exosomes, which are one method of cellular communication, are endosomal-derived small vesicles that are released by donor cells and delivered to the target cells at both short and long distances. Because exosomes carry a variety of cargoes, including proteins, mRNAs, microRNAs and other noncoding RNAs originating from donor cells, exosomes convey cellular information that enables them to potentially serve as biomarkers and therapeutics in liver diseases. Hepatocytes release exosomes to neighboring hepatocytes or nonparenchymal cells to regulate liver regeneration and repair. Nonparenchymal cells, including hepatic stellate cells, liver sinusoidal endothelial cells, and cholangiocytes, also secrete exosomes to regulate liver remodeling upon liver injury. Exosomes that are released from liver cancer cells create a favorable microenvironment for cancer growth and progression. In this review, we summarize and discuss the current findings and understanding of exosome-mediated intercellular communication in the liver, with a particular focus on the function of exosomes in both health and disease. Based on the current findings, we suggest the potential applications of exosomes as biomarkers and therapeutics for liver diseases.

Citing Articles

TSH-stimulated hepatocyte exosomes modulate liver-adipose triglyceride accumulation via the TGF-β1/ATGL axis in mice.

Ma S, Wang Y, Fan S, Jiang W, Sun M, Jing M Lipids Health Dis. 2025; 24(1):81.

PMID: 40050912 PMC: 11884018. DOI: 10.1186/s12944-025-02509-6.


Circulating Extracellular Vesicles in Alcoholic Liver Disease Affect Skeletal Muscle Homeostasis and Differentiation.

Barberi L, Porcu C, Boccia C, Cosentino M, Nicoletti C, Peruzzi B J Cachexia Sarcopenia Muscle. 2025; 16(1):e13675.

PMID: 39921321 PMC: 11806195. DOI: 10.1002/jcsm.13675.


Plasma Extracellular Vesicle-derived MicroRNA Associated with Human Alpha-1 Antitrypsin Deficiency-mediated Liver Disease.

Oshins R, Huo Z, Greenberg Z, Clark V, Duarte S, Zhou H J Clin Transl Hepatol. 2025; 13(2):118-129.

PMID: 39917464 PMC: 11797821. DOI: 10.14218/JCTH.2024.00253.


Spatial heterogeneity of the hepatocellular carcinoma microenvironment determines the efficacy of immunotherapy.

Zhang M, Huang K, Yin Q, Wu X, Zhu M, Li M Discov Oncol. 2025; 16(1):15.

PMID: 39775241 PMC: 11706828. DOI: 10.1007/s12672-025-01747-5.


Sinusoidal communication in chronic liver disease.

Gibert-Ramos A, Andres-Rozas M, Pasto R, Alfaro-Retamero P, Guixe-Muntet S, Gracia-Sancho J Clin Mol Hepatol. 2024; 31(1):32-55.

PMID: 39355871 PMC: 11791556. DOI: 10.3350/cmh.2024.0734.


References
1.
Barile L, Vassalli G . Exosomes: Therapy delivery tools and biomarkers of diseases. Pharmacol Ther. 2017; 174:63-78. DOI: 10.1016/j.pharmthera.2017.02.020. View

2.
Qi H, Liu C, Long L, Ren Y, Zhang S, Chang X . Blood Exosomes Endowed with Magnetic and Targeting Properties for Cancer Therapy. ACS Nano. 2016; 10(3):3323-33. DOI: 10.1021/acsnano.5b06939. View

3.
Li X, Liu R, Huang Z, Gurley E, Wang X, Wang J . Cholangiocyte-derived exosomal long noncoding RNA H19 promotes cholestatic liver injury in mouse and humans. Hepatology. 2018; 68(2):599-615. PMC: 6085159. DOI: 10.1002/hep.29838. View

4.
Horibe S, Tanahashi T, Kawauchi S, Murakami Y, Rikitake Y . Mechanism of recipient cell-dependent differences in exosome uptake. BMC Cancer. 2018; 18(1):47. PMC: 5756423. DOI: 10.1186/s12885-017-3958-1. View

5.
Fang T, Lv H, Lv G, Li T, Wang C, Han Q . Tumor-derived exosomal miR-1247-3p induces cancer-associated fibroblast activation to foster lung metastasis of liver cancer. Nat Commun. 2018; 9(1):191. PMC: 5768693. DOI: 10.1038/s41467-017-02583-0. View