Leucine-rich repeat-containing G-protein-coupled receptor 2 (LGR2) can regulate PO activity and AMP genes expression in Macrobrachium nipponense

Mol Immunol. 2020 Oct:126:14-24. doi: 10.1016/j.molimm.2020.07.013. Epub 2020 Jul 30.

Abstract

Leucine-rich repeat-containing G-protein-coupled receptors (LGRs) form a subfamily of the large superfamily of G-protein-coupled receptors. LGRs can be divided into three groups. LGR2 from Drosophila melanogaster is involved in cuticle tanning (melanization and sclerotization). In this study, one LGR2 (MnLGR2) was identified from Macrobrachium nipponense. MnLGR2 has an open reading frame of 4515 bp encoding a protein with 1504 amino acids. MnLGR2 is comprised of a 7-transmembrane domain, 12 leucine-rich repeats, and 5 low-complexity regions. The highest expression level of MnLGR2 was observed in gills. The expression levels of MnLGR2 in gills and stomach could be regulated by bacterial challenge. Knockdown of MnLGR2 upregulated the expression of anti-microbial peptide (AMP) genes. Further study indicated that inhibition of AMP expression by MnLGR2 was through inhibition of relish-mediated AMP expression. In addition to the negative regulation of AMP expression, MnLGR2 participated in positive regulation of phenol oxidase (PO) activity and expression of proPO activating pathway-related genes (proPO-activating factor and proPO-activating enzymes). Therefore, MnLGR2 plays an important role in prawn innate immunity.

Keywords: Anti-microbial peptide (AMP); LGR2; Macrobrachium nipponense; Phenol oxidase; Relish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / immunology
  • Antimicrobial Cationic Peptides / metabolism
  • Arthropod Proteins / genetics
  • Arthropod Proteins / immunology
  • Arthropod Proteins / metabolism*
  • Gastric Mucosa / metabolism
  • Gene Knockdown Techniques
  • Gills / metabolism
  • Host Microbial Interactions / immunology
  • Immunity, Innate
  • Leucine-Rich Repeat Proteins
  • Molting / physiology
  • Monophenol Monooxygenase / metabolism
  • Palaemonidae / microbiology
  • Palaemonidae / physiology*
  • Proteins / genetics
  • Proteins / metabolism*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction / immunology*
  • Staphylococcus aureus / immunology
  • Transcription Factors
  • Up-Regulation / immunology
  • Vibrio parahaemolyticus / immunology
  • White spot syndrome virus 1 / immunology

Substances

  • Antimicrobial Cationic Peptides
  • Arthropod Proteins
  • Leucine-Rich Repeat Proteins
  • Proteins
  • Receptors, G-Protein-Coupled
  • Transcription Factors
  • Monophenol Monooxygenase