» Articles » PMID: 34456873

Purinergic Signaling in Liver Pathophysiology

Overview
Specialty Endocrinology
Date 2021 Aug 30
PMID 34456873
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Extracellular nucleosides and nucleotides activate a group of G protein-coupled receptors (GPCRs) known as purinergic receptors, comprising adenosine and P2Y receptors. Furthermore, purinergic P2X ion channels are activated by ATP. These receptors are expressed in liver resident cells and play a critical role in maintaining liver function. In the normal physiology, these receptors regulate hepatic metabolic processes such as insulin responsiveness, glycogen and lipid metabolism, and bile secretion. In disease states, ATP and other nucleotides serve as danger signals and modulate purinergic responses in the cells. Recent studies have demonstrated that purinergic receptors play a significant role in the development of metabolic syndrome associated non-alcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), fibrosis, hepatocellular carcinoma (HCC) and liver inflammation. In this concise review, we dissect the role of purinergic signaling in different liver resident cells involved in maintaining healthy liver function and in the development of the above-mentioned liver pathologies. Moreover, we discuss potential therapeutic strategies for liver diseases by targeting adenosine, P2Y and P2X receptors.

Citing Articles

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.


Purinergic signaling in liver disease: calcium signaling and induction of inflammation.

Ulrich H, Glaser T, Thomas A Purinergic Signal. 2024; .

PMID: 39320433 DOI: 10.1007/s11302-024-10044-9.


Purinergic Signaling in Non-Parenchymal Liver Cells.

Mata-Martinez E, Ramirez-Ledesma M, Vazquez-Victorio G, Hernandez-Munoz R, Diaz-Munoz M, Vazquez-Cuevas F Int J Mol Sci. 2024; 25(17).

PMID: 39273394 PMC: 11394727. DOI: 10.3390/ijms25179447.


Inflammatory response and parasite regulation in acute toxoplasmosis: the role of P2X7 receptor in controlling virulent atypical genotype strain of .

Prado-Rangel T, Moreira-Souza A, da Silva S, Barboza-Araujo T, Castro-Junior A, Ramos I Front Immunol. 2024; 15:1452828.

PMID: 39267751 PMC: 11390460. DOI: 10.3389/fimmu.2024.1452828.


Activation of hepatic adenosine A1 receptor ameliorates MASH via inhibiting SREBPs maturation.

Zhu W, Hong Y, Tong Z, He X, Li Y, Wang H Cell Rep Med. 2024; 5(3):101477.

PMID: 38508143 PMC: 10983109. DOI: 10.1016/j.xcrm.2024.101477.


References
1.
Wei Q, Zhang Y, Sun L, Jia X, Huai W, Yu C . High dose of extracellular ATP switched autophagy to apoptosis in anchorage-dependent and anchorage-independent hepatoma cells. Purinergic Signal. 2013; 9(4):585-98. PMC: 3889388. DOI: 10.1007/s11302-013-9369-0. View

2.
Keppens S, Vandekerckhove A, DE WULF H . Characterization of the purinoceptors present in rabbit and guinea pig liver. Eur J Pharmacol. 1990; 182(1):149-53. DOI: 10.1016/0014-2999(90)90504-y. View

3.
Alchera E, Rolla S, Imarisio C, Bardina V, Valente G, Novelli F . Adenosine A2a receptor stimulation blocks development of nonalcoholic steatohepatitis in mice by multilevel inhibition of signals that cause immunolipotoxicity. Transl Res. 2016; 182:75-87. DOI: 10.1016/j.trsl.2016.11.009. View

4.
Anselmi F, Hernandez V, Crispino G, Seydel A, Ortolano S, Roper S . ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear. Proc Natl Acad Sci U S A. 2008; 105(48):18770-5. PMC: 2596208. DOI: 10.1073/pnas.0800793105. View

5.
Roden M, Shulman G . The integrative biology of type 2 diabetes. Nature. 2019; 576(7785):51-60. DOI: 10.1038/s41586-019-1797-8. View