Characterization of Dog Interleukin-2 Activity
[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.
[发布日期] [发布机构]
[效力级别] [学科分类] 兽医学
[关键词] canine;interleukin-2;lymphocyte;lymphokine-activated killer cell;tumor [时效性]