4.8 Article

Identification of a Novel Pattern Recognition Receptor DM9 Domain Containing Protein 4 as a Marker for Pro-Hemocyte of Pacific Oyster Crassostrea gigas

Journal

FRONTIERS IN IMMUNOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2020.603270

Keywords

Crassostrea gigas; DM9 domain; pattern recognition; innate immune response; pro-hemocytes

Categories

Funding

  1. National Key RD Program [2018YFD0900502]
  2. National Natural Science Foundation of China [U1706204, 41961124009]
  3. Outstanding Talents and Innovative teams of Agricultural Scientific Research and Earmarked Fund from Modern Agro-industry Technology Research System [CARS-49]
  4. Fund for Outstanding Talents and Innovative Team of Agricultural Scientific Research in Ministry of Agriculture
  5. Research Foundation for Distinguished Professor in Liaoning [XLYC1902012]
  6. Climbing Scholar in Liaoning

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A novel member of DM9 domain containing protein, CgDM9CP-4, was identified from Pacific oyster, shown to be a mannose-specific binding pattern-recognition receptor enriched in hemocytes and gill. Its transcripts level were decreased after various pathogen stimulations. The recombinant protein displayed broad binding spectrum and was mainly expressed in non-phagocytic cells. This suggests its potential role in immune recognition of pathogens.
DM9 refers to an uncharacterized protein domain that is originally discovered in Drosophila melanogaster. Two proteins with DM9 repeats have been recently identified from Pacific oyster Crassostrea gigas as mannose-specific binding pattern-recognition receptors (PRRs). In the present study, a novel member of DM9 domain containing protein (designated as CgDM9CP-4) was identified from C. gigas. CgDM9CP-4, about 16 kDa with only two tandem DM9 domains, was highly enriched in hemocytes and gill. The transcripts level of CgDM9CP-4 in circulating hemocytes were decreased after LPS, PGN and Vibrio splendidus stimulations. The recombinant protein of CgDM9CP-4 (rCgDM9CP-4) displayed a broad binding spectrum towards various pathogen-associated molecular patterns (PAMPs) (LPS, PGN, beta-glucan and Mannose) and microorganisms (Staphylococcus aureus, Micrococcus luteus, V. splendidus, V. anguillarum, Escherichia coli, Pichia pastoris and Yarrowia lipolytica). CgDM9CP-4 was mostly expressed in gill and some of the hemocytes. Flow cytometry analysis demonstrated that the CgDM9CP-4-positive hemocytes accounted for 7.3% of the total hemocytes, and they were small in size and less in granularity. CgDM9CP-4 was highly expressed in non-phagocytes (similar to 82% of total hemocytes). The reactive oxygen species (ROS) and the expression levels of cytokines in CgDM9CP-4-positive hemocytes were much lower than that in CgDM9CP-4-negative hemocytes. The mRNA expression level of CgDM9CP-4 in hemocytes was decreased after RNAi of hematopoietic-related factors (CgGATA, CgRunt, CgSCL, and CgNotch). In addition, CgDM9CP-4-positive cells were found to be much more abundant in hemocytes from gill than that from hemolymph, with most of them located in the gill filament. All these results suggested that CgDM9CP-4 was a novel member of PRR that expressed in undifferentiated pro-hemocytes to mediate immune recognition of pathogens.

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