Gasbarre L C, Urban J F, Romanowski R D
Vet Immunol Immunopathol. 1984 Jan;5(3):221-36. doi: 10.1016/0165-2427(84)90036-9.
Interleukin 2 (IL2) or T cell growth factor (TCGF) has been characterized in a number of species but not in porcines. Porcine IL2 was detected in supernates (SN) of cultures of pig lymphocytes by: 1) the stimulation of the IL2-sensitive murine T cell line, CT6; 2) a costimulator assay involving porcine thymocytes; and 3) by the in vitro maintenance of antigen or mitogen-induced porcine lymphoblastoid cells. Porcine IL2 production by pig lymphocytes was induced by the mitogens Concanavalin A (Con A) Phytohemagglutiniin (PHA), and Pokeweed mitogen (PWM), but not by lipopolysaccharide (LPS). IL2 activity was demonstrated in the SN of mitogen-stimulated lymphocyte cultures as early as 24 hr after initiation of culture, reached peak levels at 48 hr, and decreased by 72 hr. Mitogens induced IL2 secretion by pig peripheral blood mononuclear cells, lymph node cells, and spleen cells, but not thymus cells. The cells responsible for IL2 production are presumptive T cells because: 1) they are nylon wool non-adherent; and 2) are non-surface-Ig bearing. In contrast, SN from cultures of surface Ig-positive cells had minimal IL2 activity. Porcine IL2 resembles rat and human IL2 in that it has an apparent molecular weight of approximately 15,000, and does not bind to DEAE-cellulose (DE-52) ion exchange columns equilibrated in 0.05 M sodium phosphate buffer (pH 7.6).
白细胞介素2(IL2)或T细胞生长因子(TCGF)已在许多物种中得到表征,但猪的尚未有报道。通过以下方法在猪淋巴细胞培养上清液(SN)中检测到猪IL2:1)刺激对IL2敏感的小鼠T细胞系CT6;2)涉及猪胸腺细胞的共刺激测定;3)通过体外维持抗原或丝裂原诱导的猪淋巴母细胞。猪淋巴细胞产生猪IL2是由丝裂原刀豆球蛋白A(Con A)、植物血凝素(PHA)和商陆丝裂原(PWM)诱导的,但不是由脂多糖(LPS)诱导。早在培养开始后24小时,在丝裂原刺激的淋巴细胞培养物的SN中就显示出IL2活性,在48小时达到峰值水平,并在72小时下降。丝裂原诱导猪外周血单个核细胞、淋巴结细胞和脾细胞分泌IL2,但不诱导胸腺细胞分泌。负责产生IL2的细胞推测为T细胞,因为:1)它们不黏附于尼龙毛;2)不带有表面免疫球蛋白。相比之下,表面免疫球蛋白阳性细胞培养物的SN具有最小的IL2活性。猪IL2与大鼠和人IL2相似,其表观分子量约为15,000,并且不与在0.05 M磷酸钠缓冲液(pH 7.6)中平衡的DEAE-纤维素(DE-52)离子交换柱结合。