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高分支(1→3)-β-D-葡聚糖OL-2给药诱导的细胞因子mRNA分析

Analysis of cytokine mRNAs induced by the administration of a highly branched (1-->3)-beta-D-glucan, OL-2.

作者信息

Nemoto J, Ohno N, Saito K, Adachi Y, Yadomae T

机构信息

Laboratory of Immunopharmacology of Microbial Products, Tokyo College of Pharmacy, Japan.

出版信息

Biol Pharm Bull. 1994 Jul;17(7):948-54. doi: 10.1248/bpb.17.948.

Abstract

OL-2, a highly branched (1-->3)-beta-D-glucan, is an antitumor glucan showing strong hematopoietic activity with weaker adjuvant activity than schizophyllan (SPG), another antitumor glucan and one which is used clinically. This paper deals with the gene expression of cytokines in mice by OL-2 and SPG in order to characterize their immunopharmacological activity. Gene expression was examined by a reverse transcriptase-polymerase chain reaction method after intraperitoneal administration of OL-2 or SPG (250 micrograms/mouse). The OL-2 administered mice strongly expressed the interleukin 1 receptor antagonist (IL-1ra) gene but SPG administered mice did not. The difference would be strongly related to the antigen-specific response between OL-2 and SPG. In the genes related to haematopoiesis, OL-2 induced G-CSF and GM-CSF, but SPG induced IL-3. These differences would relate to the pattern of haematopoietic response. Comparing the cytokine gene expression in ICR and AKR mice by OL-2 administration, the changes in cytokine gene expression were less in AKR mice administered OL-2. These findings suggest that the immunopharmacological characteristics of OL-2 are closely related, at least in part, to the activation of the complement system. The data shown in this paper also suggest that cytokine gene expression by beta-glucan would be significantly affected by the structure of these glucans.

摘要

OL-2是一种高度分支的(1→3)-β-D-葡聚糖,是一种抗肿瘤葡聚糖,具有很强的造血活性,但其佐剂活性比另一种临床上使用的抗肿瘤葡聚糖裂褶菌多糖(SPG)弱。本文研究了OL-2和SPG对小鼠细胞因子基因表达的影响,以表征它们的免疫药理活性。通过逆转录聚合酶链反应法检测腹腔注射OL-2或SPG(250微克/只小鼠)后小鼠的基因表达。注射OL-2的小鼠强烈表达白细胞介素1受体拮抗剂(IL-1ra)基因,而注射SPG的小鼠则不表达。这种差异可能与OL-2和SPG之间的抗原特异性反应密切相关。在与造血相关的基因中,OL-2诱导G-CSF和GM-CSF,而SPG诱导IL-3。这些差异可能与造血反应模式有关。通过注射OL-2比较ICR小鼠和AKR小鼠的细胞因子基因表达,注射OL-2的AKR小鼠细胞因子基因表达的变化较小。这些发现表明,OL-2的免疫药理特性至少部分与补体系统的激活密切相关。本文所示数据还表明,β-葡聚糖的细胞因子基因表达会受到这些葡聚糖结构的显著影响。

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