4.7 Article

The proliferating cell nuclear antigen (PCNA) is a potential proliferative marker in oyster Crassostrea gigas

期刊

FISH & SHELLFISH IMMUNOLOGY
卷 122, 期 -, 页码 306-315

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2022.02.018

关键词

PCNA; Crassostrea gigas; Haemocytes; Gills; EdU

资金

  1. National Key RD Program [2018YFD0900502]
  2. National Science Foundation of China [41961124009, U1706204]
  3. China Agriculture Research System of MOF and MARA
  4. Fund for Outstanding Talents and Innovative Team of Agricultural Scientific Research from MARA
  5. Liaoning Climbing Scholar
  6. Distinguished Professor of Liaoning [XLYC1902012]
  7. Innovation Team of Universities and Colleges in Liaoning Province
  8. Research Foundation for Talented Scholars in Dalian Ocean University

向作者/读者索取更多资源

In this study, a crucial replication accessory factor CgPCNA was identified from oysters and found to be highly expressed in agranulocytes and potential hematopoietic sites. The expression of CgPCNA was up-regulated after stimulation with LPS and Vibrio splendidus. These findings suggest that CgPCNA may serve as a marker for hemocyte proliferation in oysters.
Proliferating cell nuclear antigen (PCNA) is a crucial eukaryotic replication accessory factor in the regulation of DNA synthesis, which is always used as a proliferation marker for haematopoiesis in vertebrates. In the present study, a homologue of PCNA (named as CgPCNA) with a conserved N-terminal PCNA domain and a C-terminal PCNA domain was identified from oyster Crassostrea gigas. The deduced amino acid sequence of CgPCNA shared 85.4% and 86.6% similarities with the PCNAs identified in Mus musculus and Homo sapiens, respectively. CgPCNA was firstly clustered with PCNAs from molluscs, and then with PCNAs from arthropods to form a group falling into the invertebrate clade in the phylogenic tree. The mRNA transcripts of CgPCNA were detected in all tested tissues with higher expression level in gonad, gills and haemolymph. They were also detected in granulocytes, semi-granulocytes and agranulocytes with no significant differences, but the protein level of CgPCNA in agranulocytes was significantly higher (3.67-fold, p < 0.05) than that in granulocytes. In the haemocytes, CgPCNA was mainly distributed in the nucleus and less in the cytoplasm of haemocytes. CgPCNA protein was observed at the tubule lumen regions of gills vessels, and especially colocalized with the EdU signals. After lipopolysaccharide (LPS) and Vibrio splendidus stimulation, the expression level of CgPCNA mRNA in haemocytes was significantly (p < 0.05) up-regulated at 6 h and 12 h, which was 13.87-fold and 3.89-fold of that in control, respectively. In the oysters treated with the recombinant protein CgAstakine (rCgAstakine), the protein abundance of CgPCNA was enhanced in agranulocytes and gills, while no significant change was observed in semi granulocytes and granulocytes. These results collectively indicated that CgPCNA was highly expressed in the newborn agranulocytes and the potential haematopoietic sites, and it might be applied as a marker for haemocytes proliferation in oysters.

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