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免疫干扰素部分纯化制剂引起的直接细胞溶解作用。

Direct cytolysis by partially-purified preparations of immune interferon.

作者信息

Tyring S, Klimpel G R, Fleischmann W R, Baron S

出版信息

Int J Cancer. 1982 Jul 15;30(1):59-64. doi: 10.1002/ijc.2910300111.

Abstract

Mouse IFN gamma preparations purified 30-fold were found to have direct cytolytic activity against a number of tumor and normal cells. Cell killing was determined using a sensitive, rapid and accurate assay which employed very low numbers of cells and very small quantities of interferon. The cytolytic activity of IFN gamma on 11 murine tumor cell lines was investigated. A 20-fold difference was found between the most-sensitive cell type, P-388 lymphoma, versus the most resistant cell type, C127v leukemia. A number of normal mouse cells was also found to have low to intermediate sensitivity to the cytolytic action of IFN gamma. Human IFN gamma was also shown to have cytolytic activity which, like mouse IFN gamma, was relatively species-specific. Direct cytolysis was not found to be a characteristic of IFN-alpha/beta. Different mechanisms of action for the antiviral and cytolytic activities of IFN gamma are indicated because the cytolytic titer of IFN gamma did not parallel its antiviral titer on most cell types and increasing the cell number produced a decrease in the cytolytic titer and an increase in the anti-viral titer. High concentrations of IFN gamma (i.e., 2,900 units/ml) resulted in complete lysis of cells within 24 h, while lower concentrations (i.e., 700 units/ml) resulted in a reversible inhibition of cell growth during this time period. Evidence that the cytolytic substance in the IFN gamma preparation was IFN gamma include the following: (1) both antiviral and anticellular activities copurified through a 30-fold purification; and both activities were (2) relatively species-specific; (3) sensitive to heat; (4) inactivated by low pH and (5) neutralized by antibodies to IFN gamma. Therefore, we propose the possibility that direct cytolysis is yet another of IFN gamma's distinctive antivities.

摘要

经30倍纯化的小鼠γ干扰素制剂被发现对多种肿瘤细胞和正常细胞具有直接的细胞溶解活性。使用一种灵敏、快速且准确的检测方法来测定细胞杀伤情况,该方法使用的细胞数量极少且干扰素用量也很少。研究了γ干扰素对11种小鼠肿瘤细胞系的细胞溶解活性。发现最敏感的细胞类型P-388淋巴瘤与最耐药的细胞类型C127v白血病之间存在20倍的差异。还发现一些正常小鼠细胞对γ干扰素的细胞溶解作用具有低至中等的敏感性。人γ干扰素也显示出细胞溶解活性,与小鼠γ干扰素一样,具有相对的种属特异性。未发现直接细胞溶解是α/β干扰素的特征。γ干扰素的抗病毒和细胞溶解活性存在不同的作用机制,因为γ干扰素的细胞溶解效价在大多数细胞类型上与其抗病毒效价并不平行,增加细胞数量会导致细胞溶解效价降低而抗病毒效价升高。高浓度的γ干扰素(即2900单位/毫升)在24小时内导致细胞完全裂解,而较低浓度(即700单位/毫升)在此时间段内导致细胞生长的可逆抑制。γ干扰素制剂中的细胞溶解物质为γ干扰素的证据包括以下几点:(1)抗病毒和抗细胞活性在30倍纯化过程中共同纯化;(2)两种活性都具有相对种属特异性;(3)对热敏感;(4)在低pH下失活;(5)被γ干扰素抗体中和。因此,我们提出直接细胞溶解可能是γ干扰素另一种独特活性的可能性。

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