Abstract
Mammalian granulocyte colony-stimulating factor (G-CSF; CSF3) is a primary cytokine that promotes the development, mobilization, and activation of neutrophils and their precursors. Teleosts have been reported to possess two paralogs as a likely result of the teleost-wide whole genome duplication (WGD) event, but functional divergence of G-CSF paralogs remains poorly understood. Common carp are an allotetraploid species owing to an additional WGD event in the carp lineage and here, we report on genomic synteny, sequence similarity, and phylogeny of four common carp G-CSF paralogs (g-csfa1 and g-csfa2; g-csfb1 and g-csfb2). G-csfa1 and g-csfa2 show differential and relatively high gene expression levels, while g-csfb1 and g-csfb2 show low basal gene expression levels in most tissues. All paralogs are expressed higher in macrophages than in other leukocyte sub-types and are highly up-regulated by treatment of macrophages with mitogens. Recombinant G-CSFa1 and G-CSFb1 both promoted the proliferation of kidney hematopoietic cells, while only G-CSFb1 induced the differentiation of kidney cells along the neutrophil-lineage. Colony-forming unit assays revealed that G-CSFb1 alone stimulates the formation of CFU-G colonies from head- A nd trunk-kidney whereas the combination of G-CSFa1 and G-CSFb1 stimulates the formation of both CFU-G and CFU-GM colonies. Recombinant G-CSFa1 and G-CSFb1 also exhibit chemotactic activity against kidney neutrophils and up-regulation of cxcr1 mRNA expression was highest in neutrophils after G-CSFb1 stimulation. Furthermore, G-CSFb1 more than G-CSFa1 induced priming of kidney neutrophils through up-regulation of a NADPH-oxidase component p47phox. In vivo administration of G-CSF paralogs increased the number of circulating blood neutrophils of carp. Our findings demonstrate that gene duplications in teleosts can lead to functional divergence between paralogs and shed light on the sub-functionalization of G-CSF paralogs in cyprinid fish.
| Original language | English |
|---|---|
| Article number | 255 |
| Number of pages | 18 |
| Journal | Frontiers in Immunology |
| Volume | 10 |
| DOIs | |
| Publication status | Published - 19 Feb 2019 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2019 Frew.
Funding
This work was supported in part by a Grant-in Aid for Young Scientists (B) (16K18752) from the Japan Society for the Promotion of Science (JSPS) to FK and a grant of International joint research and training of young researchers for zoonosis control in the globalized world (S1491007) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) Japan. AW was funded by the European Commission under the 8th (H2020) Framework Program for Research and Technological Development of the European Union (PARAFISHCONTROL Grant No. 634429).
Keywords
- Cell Migration
- Granulocyte Colony-Stimulating Factor
- Hematopoiesis
- Neutrophil
- Respiratory Burst
- Teleost
- Gene Expression/physiology
- Leukocytes/metabolism
- Neutrophils/metabolism
- Up-Regulation/physiology
- Carps/metabolism
- Macrophages/metabolism
- Cell Proliferation/physiology
- Hematopoietic Stem Cells/metabolism
- Leukocyte Count/methods
- Phylogeny
- Kidney/metabolism
- Granulocyte Colony-Stimulating Factor/metabolism
- Animals
- NADPH Oxidases/metabolism
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