Molecular cloning and characterization of Foxp3 in Atlantic salmon ( Salmo salar)
Foxp3 is a T cell-specific transcription factor and plays a key role in the development of Treg cells and in the immune regulatory process during inflammation. Here we report cloning and characterization of the full-length cDNA of Atlantic salmon Foxp3, which possesses a Forkhead domain, a zinc fing...
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Veröffentlicht in: | Fish & shellfish immunology 2011-03, Vol.30 (3), p.902-909 |
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Sprache: | eng |
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Zusammenfassung: | Foxp3 is a T cell-specific transcription factor and plays a key role in the development of Treg cells and in the immune regulatory process during inflammation. Here we report cloning and characterization of the full-length cDNA of Atlantic salmon Foxp3, which possesses a Forkhead domain, a zinc finger domain and a leucine-zipper domain as its counterpart in mammals. Foxp3 is highly expressed in thymus. Furthermore, regulated expression was observed in head kidney cells in response to β-glucan and mitogens (LPS and ConA), and in the head kidney, spleen and liver after intraperitoneal injection of live
Aeromonas salmonicida. In addition, transfection of CHSE-214 cells with salmon Foxp3 fused with a C-termial RFP tag, resulted in the expression of the transgene in and close to the nuclei upon stimulation. Taken together, these results suggest the presence of a Foxp3 gene in Atlantic salmon that may be an important transcription factor in immune regulation, and further research may reveal the existence of Treg-like T cells in this species.
► Regulatory T cell marker gene Foxp3 of Atlantic salmon is cloned and characterised. ► Foxp3 is highly expressed in thymus. ► Foxp3 mRNA expression is modulated in leukocytes by mitogens and β-glucan. ► Foxp3 mRNA expression is increased in the head kidney after Aeromonas salmonicida infection. ► Transfection of CHSE-214 cells with salmon Foxp3 fused with a C-termial RFP tag, resulted in the expression of the transgene in and close to the nuclei upon stimulation. |
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ISSN: | 1050-4648 1095-9947 |
DOI: | 10.1016/j.fsi.2011.01.012 |