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盘基网柄菌细胞死亡的环二鸟苷酸诱导需要聚酮化合物DIF-1。

c-di-GMP induction of Dictyostelium cell death requires the polyketide DIF-1.

作者信息

Song Yu, Luciani Marie-Françoise, Giusti Corinne, Golstein Pierre

机构信息

Centre d'Immunologie de Marseille-Luminy, UM2 Aix-Marseille Université; Institut National de la Santé et de la Recherche Médicale, U1104; and Centre National de la Recherche Scientifique, UMR7280, 13288 Marseille, France.

Centre d'Immunologie de Marseille-Luminy, UM2 Aix-Marseille Université; Institut National de la Santé et de la Recherche Médicale, U1104; and Centre National de la Recherche Scientifique, UMR7280, 13288 Marseille, France

出版信息

Mol Biol Cell. 2015 Feb 15;26(4):651-8. doi: 10.1091/mbc.E14-08-1337. Epub 2014 Dec 17.

Abstract

Cell death in the model organism Dictyostelium, as studied in monolayers in vitro, can be induced by the polyketide DIF-1 or by the cyclical dinucleotide c-di-GMP. c-di-GMP, a universal bacterial second messenger, can trigger innate immunity in bacterially infected animal cells and is involved in developmental cell death in Dictyostelium. We show here that c-di-GMP was not sufficient to induce cell death in Dictyostelium cell monolayers. Unexpectedly, it also required the DIF-1 polyketide. The latter could be exogenous, as revealed by a telling synergy between c-di-GMP and DIF-1. The required DIF-1 polyketide could also be endogenous, as shown by the inability of c-di-GMP to induce cell death in Dictyostelium HMX44A cells and DH1 cells upon pharmacological or genetic inhibition of DIF-1 biosynthesis. In these cases, c-di-GMP-induced cell death was rescued by complementation with exogenous DIF-1. Taken together, these results demonstrated that c-di-GMP could trigger cell death in Dictyostelium only in the presence of the DIF-1 polyketide or its metabolites. This identified another element of control to this cell death and perhaps also to c-di-GMP effects in other situations and organisms.

摘要

在体外单层培养中对模式生物盘基网柄菌的细胞死亡进行研究时发现,聚酮化合物DIF-1或环状二核苷酸c-di-GMP均可诱导细胞死亡。c-di-GMP作为一种通用的细菌第二信使,可在细菌感染的动物细胞中触发先天免疫,并且参与盘基网柄菌的发育性细胞死亡。我们在此表明,c-di-GMP不足以诱导盘基网柄菌细胞单层的细胞死亡。出乎意料的是,它还需要DIF-1聚酮化合物。c-di-GMP与DIF-1之间显著的协同作用表明,后者可以是外源性的。所需的DIF-1聚酮化合物也可以是内源性的,这表现为在对DIF-1生物合成进行药理学或遗传学抑制后,c-di-GMP无法在盘基网柄菌HMX44A细胞和DH1细胞中诱导细胞死亡。在这些情况下,通过外源性DIF-1互补可挽救c-di-GMP诱导的细胞死亡。综上所述,这些结果表明,c-di-GMP仅在存在DIF-1聚酮化合物或其代谢产物的情况下才能触发盘基网柄菌的细胞死亡。这确定了这种细胞死亡以及可能在其他情况和生物体中c-di-GMP效应的另一个控制因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/4325836/583bb4b50d02/651fig1.jpg

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