Journal of Veterinary Medical Science | |
Characterization of Dog Interleukin-2 Activity | |
Toru FUJINAGA1  Mitsuyoshi HAGIO1  Shinya MIZUNO1  | |
关键词: canine; interleukin-2; lymphocyte; lymphokine-activated killer cell; tumor; | |
DOI : 10.1292/jvms.55.925 | |
学科分类:兽医学 | |
来源: Japanese Society of Veterinary Science | |
【 摘 要 】
References(30)Cited-By(2)Proliferative activity of murine interleukin-2 (IL-2) dependent T cells (CTLL-2) was detected in the culture supernatant of canine peripheral blood lymphocytes (PBL) stimulated with phytohemagglutinin-P (PHA-P), and was defined as dog IL-2. The highest production of IL-2 was obtained under the conditions in which a PBL population of 2×106 cells/ml was stimulated with PHA-P at a concentration of 10μg/ml at 38°C for 48 hr. Dog IL-2 activity was significantly inhibited by heating at 65°C, acidification under pH 4, alkalification over pH 10, and trypsin exposure. A peak of dog IL-2 activity was detected in the fraction with a molecular weight of approximately 31, 000 by gel filtration. Long-term culture of canine lymphocytes was successful over 10 passages by using dog IL-2 with PHA-P-stimulation every 3 passages. The cultured cells mostly consisted of small- and medium-sized lymphocytes. These cells reacted to anti-dog thymocyte rabbit serum and anti-dog Thy-1 mouse monoclonal antibody. These cells were therefore considered to originate in T-lineage lymphocytes. Cytostasis of PBL from intact dogs reacting to canine transmissible venereal sarcoma cells was increased significantly when PBL was cultured for more than 30 days with homologous IL-2.
【 授权许可】
Unknown
【 预 览 】
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