Satoh M, Ichimura O, Mitsuno T, Kojima E, Osawa T
J Pharmacobiodyn. 1982 Oct;5(10):818-28. doi: 10.1248/bpb1978.5.818.
The level of colony stimulating factors (CSF) in mouse serum was elevated by a single intraperitoneal injection of PSK, a host-mediated antitumor protein-bound polysaccharide obtained from Basidiomycetes. The assay for CSF activity was performed by employing a semisolid methylcellulose culture method using mouse bone marrow cells, and the activity was estimated by an equation well matched with the dose response curve obtained in the CSF assay. A temporary increase of CSF activity within 10 h after the injection of an antitumor polysaccharide, Krestin (PSK) (250-1000 mg/kg) was followed by a fast decline in the activity, but no significant increases were detected in the cases of 62.5 and 125 mg/kg PSK injections. The CSF activity in PSK (500 mg/kg)-treated mouse serum was separated into two active fractions by DEAE ion-exchange chromatography, and both fractions were found to induce colonies comprised of cells with the properties of macrophage in regard to morphology, cytochemistry of non-specific esterase, phagocytic function and expression of Fc receptors on the cell surface. The elevation of the serum CSF level due to administration of so-called host-mediated antitumor agents might be one of the tumor-defense mechanisms in vivo.
通过单次腹腔注射PSK(一种从担子菌中获得的宿主介导的抗肿瘤蛋白结合多糖),小鼠血清中的集落刺激因子(CSF)水平升高。采用半固体甲基纤维素培养法,利用小鼠骨髓细胞进行CSF活性测定,并通过与CSF测定中获得的剂量反应曲线高度匹配的公式来估算活性。注射抗肿瘤多糖克瘤宁(PSK)(250 - 1000 mg/kg)后10小时内CSF活性暂时升高,随后活性迅速下降,但注射62.5和125 mg/kg PSK时未检测到明显升高。用DEAE离子交换色谱法将PSK(500 mg/kg)处理的小鼠血清中的CSF活性分离为两个活性部分,发现这两个部分均能诱导形成由具有巨噬细胞特性的细胞组成的集落,这些特性包括形态学、非特异性酯酶的细胞化学、吞噬功能以及细胞表面Fc受体的表达。由于施用所谓的宿主介导的抗肿瘤药物而导致血清CSF水平升高,可能是体内肿瘤防御机制之一。