P2X4 receptors mediate induction of antioxidants, fibrogenic cytokines and ECM transcripts; in presence of replicating HCV in in vitro setting: An insight into role of P2X4 in fibrosis

• Published in: PloS one Vol. 17; no. 5; p. e0259727
• Main Authors: Manzoor, Sobia, Khalid, Madiha, Idrees, Muhammad
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 20.05.2022; Public Library of Science (PLoS)
• Subjects: Adenosine; Analysis; Angiotensin; Angiotensin II; Angiotensin II - metabolism; Animals; Antioxidants; Biology and life sciences; Carcinoma, Hepatocellular - pathology; Cell culture; Chronic illnesses; Cirrhosis; Cloning; Copper; Cytokines; Cytokines - metabolism; Elastin; Elastin - metabolism; Enzymes; Extracellular matrix; Fibrosis; Gene expression; Genetic aspects; Genomes; Health aspects; Hepacivirus - genetics; Hepacivirus - physiology; Hepatitis; Hepatitis C; Hepatitis C - metabolism; Hepatitis C virus; Hepatocellular carcinoma; Hepatocytes; Homeostasis; Humans; Infections; Inflammation; Laminin; Laminin - metabolism; Leptin; Liver cancer; Liver cirrhosis; Liver diseases; Liver Neoplasms - pathology; Medicine and health sciences; Optimization; Pathogenesis; Plasmids; Proteins; Rats; Receptors; Receptors, Purinergic P2X4 - metabolism; Research and Analysis Methods; Transforming Growth Factor beta - metabolism; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-α; Vasoactive agents; Pakistan; Saudi Arabia
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0259727

Major HCV infections lead to chronic hepatitis, which results in progressive liver disease including fibrosis, cirrhosis and eventually hepatocellular carcinoma (HCC). P2X4 and P2X7 are most widely distributed receptors on hepatocytes. Full length P2X4 (1.7kb) (Rattus norvegicus) was sub cloned in mammalian expression vector pcDNA3.1+. Two stable cell lines 293T/P2X4 (experimental) and 293T/ NV or null vector (control) were established. Both cell lines were inoculated with high viral titers human HCV sera and control human sera. Successfully infected cells harvested on day 5 and day 9 of post infection were used for further studies. The results revealed a significant increase in gene expression of P2X4 on day 5 and day 9 Post -infection in cells infected with HCV sera compared with cells inoculated with control sera. Quantitative real time PCR analysis revealed that HO-1 was significantly upregulated in presence of P2X4 in HCV infected cells (P2X4/HCV) when compared with control NV/HCV cells. A significant decrease was observed in expression of Cu/ZnSOD in presence of P2X4 in HCV infected cells compared to control NV/HCV cells. However, expression of both antioxidants was observed unaltered in cells harvested on day 9 post infection. Gene expression of angiotensin II significantly increased in HCV infected cells in presence of P2X4 on day 5 and day 9 of post infection when compared with control NV/HCV cells. A significant increase in gene expression of TNF-α and TGF-β was observed in HCV infected cells in presence of P2X4 on day 9 post infection in comparison with control (NV/HCV cells). However, gene expression of adipokine leptin was not affected in both experimental (P2X4/HCV) and control (NV/HCV) groups on day 5 and day 9 of post infection. Extracellular matrix proteins, laminin and elastin genes expression also significantly increased in presence of P2X4 (HCV/P2X4) on day 9 of post-infection compared to control group NV/HCV cells. In conclusion, these findings constitute the evidence that P2X4 receptors in the presence of HCV play a significant role in the regulation of key antioxidant enzymes (HO-1, Cu/ZnSOD), in the induction of proinflammatory. cytokine (TNF-α), profibrotic cytokine (TGF-β) vasoactive cytokine (angiotensin II). P2X4 also increases the expression of extracellular matrix proteins (laminin and elastin) in the presence of HCV.