Investigation into imbalance of Th1/Th2 cells in cirrhotic, hypersplenic rats

J Int Med Res. 2020 Mar;48(3):300060519889441. doi: 10.1177/0300060519889441. Epub 2019 Dec 18.

Abstract

Objectives: To evaluate the Th1/Th2 cell profile in spleens of cirrhotic and hypersplenic rats by investigating the expression of Th1-associated chemokine receptors CXCR3, CCR5 and Th2-associated chemokine receptor CCR3.

Methods: Experimental liver cirrhosis and hypersplenism were induced in rats by the intragastric administration of carbon tetrachloride (CCl4; 40% solution [0.3 ml/100g, twice/week for 8 weeks]) and confirmed by pathology and hemogram. Presence of the three chemokine receptors was investigated by real-time polymerase chain reaction (RT-PCR), immunohistochemical staining, and western blot analysis.

Results: By comparison with control animals (n=10), RT-PCR demonstrated that CXCR3 and CCR5-mRNA levels were significantly elevated in the hypersplenic rats (n=26) and CCR3-mRNA levels were lower. Immunohistochemical staining showed that by comparison with controls, the mean density of the Th1-associated CXCR3 and CCR5 receptors was significantly increased but there was no difference between groups in Th2-associated CCR3 receptors. Western blot analysis showed that by comparison with controls, hypersplenic rats had higher levels of CXCR3 and CCR5 protein but lower levels of CCR3 protein.

Conclusions: The abnormal expression of Th1-associated chemokine receptors in spleens of rats with cirrhosis and hypersplenism induced by CCL4 suggests that a functional imbalance between Th1/Th2 cells may play a role in the pathogenesis of hypersplenism.

Keywords: Liver cirrhosis; animal model; chemokine receptors; hypersplenism; lymphocytes.

MeSH terms

  • Animals
  • Housing, Animal
  • Hypersplenism*
  • Liver Cirrhosis / chemically induced
  • Liver Cirrhosis / genetics
  • Liver Cirrhosis / pathology
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, CCR5 / genetics
  • Th1 Cells*
  • Th2 Cells*

Substances

  • Receptors, CCR5