P38 is involved in immune response by regulating inflammatory cytokine expressions in the Pacific oyster Crassostrea gigas

Dev Comp Immunol. 2019 Feb:91:108-114. doi: 10.1016/j.dci.2018.10.011. Epub 2018 Oct 29.

Abstract

P38 mitogen-activated protein kinases are serine/threonine protein kinases reportedly involved in the innate immunity of vertebrates and invertebrates. In the present study, a P38 homolog (CgP38) was characterized from the Pacific oyster Crassostrea gigas. The full-length cDNA of CgP38 was of 1515 bp containing a 1101 bp open reading frame. A serine/threonine protein kinase (S_TKc) domain with a conserved Thr-Gly-Tyr motif and an ATRW substrate-binding site was found in the deduced amino acid sequence of CgP38. CgP38 shared a close evolutionary relationship with ChP38 from the Hong Kong oyster Crassostrea hongkongensis. The transcript levels of CgP38 in hemocytes increased significantly from 12 h to 48 h after lipopolysaccharide (LPS) stimulation and from 12 h to 24 h after Vibrio splendidus stimulation. The phosphorylation level of CgP38 in oyster hemocytes increased significantly at 2 h after LPS stimulation. CgP38 positively regulated the expression of interleukins, such as CgIL17-1, CgIL17-2, CgIL17-3, CgIL17-4 and CgIL17-6, and tumor necrosis factor CgTNF after LPS or V. splendidus stimulation. These results suggested that CgP38 participated in oyster immune response by regulating the expressions of inflammatory cytokines.

Keywords: Interleukins; Lipopolysaccharide; Mitogen-activated protein kinase; Oysters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Cloning, Molecular
  • Crassostrea / immunology*
  • Crassostrea / microbiology
  • Cytokines / metabolism
  • Evolution, Molecular
  • Hemocytes / physiology*
  • Immunity, Innate
  • Inflammation / immunology*
  • Lipopolysaccharides / immunology
  • Phosphorylation
  • Phylogeny
  • Vibrio / physiology*
  • Vibrio Infections / immunology*
  • p38 Mitogen-Activated Protein Kinases / genetics*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Cytokines
  • Lipopolysaccharides
  • p38 Mitogen-Activated Protein Kinases