Hertel-Wulff B, Strober S
Department of Medicine, Stanford University School of Medicine, CA 94305.
J Immunol. 1988 Apr 15;140(8):2633-8.
Cloned natural suppressor (NS) cells derived from spleens of total lymphoid irradiated BALB/c mice were incubated with the phorbol ester, PMA, and calcimycin for 4 h. After thorough washing, the induced NS cells were incubated in serum-free medium for 24 h and the supernatants were collected. The supernatants suppressed the MLR between normal adult responder and stimulator spleen cells. There was no Ag specificity or H-2 haplotype restriction of the MLR suppression. The supernatants did not inhibit [3H]thymidine incorporation per se, because they did not suppress mitogen stimulation of spleen cells. Protease digestion of the supernatants removed the suppressive activity, and dialysis studies indicated that the molecular size of the suppressive factor was larger than 50,000 Da and smaller than 100,000 Da. The suppressive activity was stable at 56 degrees C, pH 2, for 1 h. Thus, NS cell clones can be induced to secrete an immunosuppressive lymphokine, NS factor.
将源自经全身淋巴照射的BALB/c小鼠脾脏的克隆天然抑制(NS)细胞与佛波酯、佛波醇酯(PMA)和离子霉素一起孵育4小时。充分洗涤后,将诱导的NS细胞在无血清培养基中孵育24小时,然后收集上清液。该上清液抑制正常成年反应细胞与刺激脾细胞之间的混合淋巴细胞反应(MLR)。MLR抑制不存在抗原特异性或H-2单倍型限制。上清液本身并不抑制[3H]胸腺嘧啶核苷掺入,因为它们不抑制脾细胞的有丝分裂原刺激。上清液经蛋白酶消化后失去抑制活性,透析研究表明抑制因子的分子大小大于50,000道尔顿且小于100,000道尔顿。抑制活性在56℃、pH 2条件下1小时内稳定。因此,NS细胞克隆可被诱导分泌一种免疫抑制性淋巴因子,即NS因子。