Up-regulation of RIP1 and IPS-1 in chronic HBV infected patients

Minoo Safari-Arababadi1, Mohammad Hossein Modarressi1,2, Mohammad Kazemi Arababadi3,4

  • 1Department of Genetics, Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Insights

Increased expression of IPS-1 and RIP1 in immune cells of chronic hepatitis B patients suggests their role in low-grade inflammation driving liver disease progression.

Area of Science:

  • Immunology
  • Virology
  • Hepatology

Background:

  • Intracytoplasmic receptors RIG1 and MDA5 recognize viral double-stranded RNA.
  • IPS-1 and RIP1 are key downstream signaling molecules in this innate immune pathway.

Purpose of the Study:

  • To investigate mRNA levels of IPS-1 and RIP1 in peripheral blood immune cells of chronic hepatitis B (CHB) patients.
  • To explore the relationship between IPS-1/RIP1 expression and CHB disease markers.

Main Methods:

  • Quantitative reverse transcription polymerase chain reaction (RT-qPCR) was used.
  • mRNA levels of IPS-1 and RIP1 were measured in 60 CHB patients and 120 healthy controls.

Main Results:

  • Significant elevation of IPS-1 and RIP1 mRNA levels was observed in CHB patients compared to healthy individuals.
  • No correlation was found between IPS-1/RIP1 expression and serum HBeAg levels or liver enzymes.

Conclusions:

  • IPS-1 and RIP1 may contribute to the chronic low-grade inflammation characteristic of CHB.
  • This inflammation is implicated in the pathogenesis of liver cirrhosis and hepatocellular carcinoma.

Related Concept Videos

EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
3.4K
iPS Cell Differentiation01:22

iPS Cell Differentiation

The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
3.0K
Epigenetic Regulation01:46

Epigenetic Regulation

Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
33.5K
GTPases and their Regulation02:14

GTPases and their Regulation

Guanine nucleotide-binding proteins (G-proteins), also known as GTPases, are a superfamily of proteins that regulate many cellular processes, such as cell signaling, vesicular transport, and the regulation of cell shape and motility. Mutation or dysfunction of these proteins can lead to disease. There are around 40,000 known G-proteins that can broadly be classified into two groups ‒  small G-proteins consisting of a single domain and large multi-domain G-proteins.
Large G-proteins,...
9.8K
Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.6K
Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
2.1K