TY - JOUR
T1 - Effects of IFNγ administration on allograft rejection in ginbuna crucian carp
AU - Shibasaki, Yasuhiro
AU - Hatanaka, Chihiro
AU - Matsuura, Yuta
AU - Miyazawa, Ryuichiro
AU - Yabu, Takeshi
AU - Moritomo, Tadaaki
AU - Nakanishi, Teruyuki
N1 - Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - In vertebrates, the rejection of allografts is primarily accomplished by cell-mediated immunity. We recently identified four IFNγ isoforms with antiviral activity in ginbuna crucian carp, Carassius auratus langsdorfii. However, involvement of the IFNγ isoforms in cell-mediated immunity, especially in T cell function remains unknown. Here we investigate expression of the IFNγ isoforms and effects of administration of recombinant IFNγ (rgIFNγ) isoforms in ginbuna scale allograft rejection. All four IFNγ isoforms showed significantly higher expression with the progression of graft rejection. Administration of rgIFNγrel 1 but not rgIFNγrel 2, rgIFNγ1 nor rgIFNγ2 enhanced allograft rejection. The number of CD4+ and CD8α+ cells increased in early stages of rejection, while sIgM+ cells were higher than controls at day 0 and 5 in the rgIFNγrel 1 administrated group. Expression of IFNγ1 and IFNγ2 mRNA was significantly up-regulated by rgIFNγrel 1 administration, while that of IFNγrel 1 and IFNγrel 2 was not. These results suggest different contributions of the four IFNγ isoforms toward the immune responses comprising allograft rejection.
AB - In vertebrates, the rejection of allografts is primarily accomplished by cell-mediated immunity. We recently identified four IFNγ isoforms with antiviral activity in ginbuna crucian carp, Carassius auratus langsdorfii. However, involvement of the IFNγ isoforms in cell-mediated immunity, especially in T cell function remains unknown. Here we investigate expression of the IFNγ isoforms and effects of administration of recombinant IFNγ (rgIFNγ) isoforms in ginbuna scale allograft rejection. All four IFNγ isoforms showed significantly higher expression with the progression of graft rejection. Administration of rgIFNγrel 1 but not rgIFNγrel 2, rgIFNγ1 nor rgIFNγ2 enhanced allograft rejection. The number of CD4+ and CD8α+ cells increased in early stages of rejection, while sIgM+ cells were higher than controls at day 0 and 5 in the rgIFNγrel 1 administrated group. Expression of IFNγ1 and IFNγ2 mRNA was significantly up-regulated by rgIFNγrel 1 administration, while that of IFNγrel 1 and IFNγrel 2 was not. These results suggest different contributions of the four IFNγ isoforms toward the immune responses comprising allograft rejection.
KW - Allograft rejection
KW - Cell-mediated immunity
KW - Ginbuna crucian carp
KW - Interferon gamma
KW - Interferon gamma related
UR - http://www.scopus.com/inward/record.url?scp=84966702135&partnerID=8YFLogxK
U2 - 10.1016/j.dci.2016.04.021
DO - 10.1016/j.dci.2016.04.021
M3 - Article
C2 - 27156851
AN - SCOPUS:84966702135
SN - 0145-305X
VL - 62
SP - 108
EP - 115
JO - Developmental and Comparative Immunology
JF - Developmental and Comparative Immunology
ER -