de la Maza L M, Peterson E M, Burton L E, Gray P W, Rinderknecht E, Czarniecki C W
Department of Pathology, University of California, Irvine 92717.
Infect Immun. 1987 Nov;55(11):2727-33. doi: 10.1128/iai.55.11.2727-2733.1987.
The effects of recombinant human gamma interferon (rHuIFN-gamma; two identical monomers of 140 residues in length) and of two re-engineered C-terminal variants, rHuIFN-gamma Tetra-Ser (residues 129 to 132 replaced by serine) and rHuIFN-gamma 125 (two identical monomers of 125 residues each with the last 14 residues plus an additional alanine from the C terminus deleted), were compared in terms of several in vitro biological activities. By using three different human cell lines (HeLa 229, HEp-2, and A549), the interferons were tested for their ability to inhibit: (i) growth of Chlamydia trachomatis; (ii) replication of encephalomyocarditis virus; and (iii) cell growth. rHuIFN-gamma restricted the growth of chlamydiae to 50% of the non-IFN-treated control at concentrations ranging from 0.01 to 0.05 ng/ml, depending on the cell type assayed. One of the modified proteins, rHuIFN-gamma Tetra-Ser, also decreased the growth of chlamydiae, but it required a concentration of approximately 0.5 ng/ml to produce 50% inhibition. rHuIFN-gamma 125 had the lowest antichlamydial activity of the three IFN-gamma variants tested; concentrations of 1 to 20 ng/ml were needed to reduce the growth of C. trachomatis to 50% of that of the control. The relative antiviral and antiproliferative activities of the three IFN-gamma preparations paralleled their antichlamydial activities in these three cell lines. The antiencephalomyocarditis virus activities of rHuIFN-gamma Tetra-Ser and rHuIFN-gamma 125 were reduced by approximately 10-fold and 10(2)- to 10(3)-fold, respectively, compared with the antiviral activity of rHuIFN-gamma. Proliferation of the three cell lines was restricted to approximately 50% of the control with 0.5 to 10 ng of rHuIFN-gamma per ml. Inhibition of cell growth by rHuIFN-gamma Tetra-Ser was significant only at concentrations equal to or greater than 30 ng/ml, and the rHuIFN-gamma 125 variant did not significantly decrease the growth of any of the three cell lines at the concentrations tested. These results suggest that the C-terminal portion of rHuIFN-gamma is critical for maintaining the conformation necessary for inducing the antichlamydial, antiviral, and antiproliferative activities of the molecule.
比较了重组人γ干扰素(rHuIFN-γ;由两个长度为140个残基的相同单体组成)以及两种重新设计的C端变体rHuIFN-γ Tetra-Ser(第129至132位残基被丝氨酸取代)和rHuIFN-γ 125(两个相同的单体,每个单体长度为125个残基,C端最后14个残基加一个额外的丙氨酸被删除)在几种体外生物学活性方面的作用。使用三种不同的人类细胞系(HeLa 229、HEp-2和A549),检测了干扰素抑制以下方面的能力:(i)沙眼衣原体的生长;(ii)脑心肌炎病毒的复制;以及(iii)细胞生长。rHuIFN-γ在浓度范围为0.01至0.05 ng/ml时,根据所检测的细胞类型,将衣原体的生长限制在未用干扰素处理的对照的50%。其中一种修饰蛋白rHuIFN-γ Tetra-Ser也能降低衣原体的生长,但需要约0.5 ng/ml的浓度才能产生50%的抑制作用。rHuIFN-γ 125在所测试的三种IFN-γ变体中抗衣原体活性最低;需要1至20 ng/ml的浓度才能将沙眼衣原体的生长降低至对照的50%。这三种IFN-γ制剂的相对抗病毒和抗增殖活性与它们在这三种细胞系中的抗衣原体活性相似。与rHuIFN-γ的抗病毒活性相比,rHuIFN-γ Tetra-Ser和rHuIFN-γ 125的抗脑心肌炎病毒活性分别降低了约10倍和10²至10³倍。每毫升0.5至10 ng的rHuIFN-γ可将三种细胞系的增殖限制在对照的约50%。rHuIFN-γ Tetra-Ser仅在浓度等于或大于30 ng/ml时对细胞生长有显著抑制作用,而rHuIFN-γ 125变体在测试浓度下未显著降低三种细胞系中任何一种的生长。这些结果表明,rHuIFN-γ的C端部分对于维持诱导该分子抗衣原体、抗病毒和抗增殖活性所需的构象至关重要。