Suppr超能文献

共生细菌诱导宿主上皮组织形态发生过程中的细胞凋亡。

Induction of apoptosis by cooperative bacteria in the morphogenesis of host epithelial tissues.

作者信息

Foster J S, McFall-Ngai M J

机构信息

Pacific Biomedical Research Center, University of Hawai'i, Honolulu, HI 96813, USA.

出版信息

Dev Genes Evol. 1998 Aug;208(6):295-303. doi: 10.1007/s004270050185.

Abstract

Associations with pathogenic bacteria have recently been shown to initiate apoptotic programs in the cells of their animal hosts, where host cell death is hypothesized to be a response of the immune system, either initiated as a mechanism of host defense or bacterial offense. In this study, we present evidence that bacterial initiation of apoptosis is neither restricted to pathogenesis nor to the initation of an immune response. In the cooperative association between the sepiolid squid Euprymna scolopes and the luminous bacterium Vibrio fischeri, the bacteria induce a dramatic morphogenesis of the host tissues during the first few days of interaction between these partners. The most striking change is the bacteria-triggered loss of an extensive superficial epithelium that potentiates the infection process. Our analyses of these tissues revealed that the bacteria induce apoptosis in the cells that comprise this epithelium within hours of the interaction with bacteria. Ultrastructural analysis revealed that after 24 h the integrity of the epithelium had been lost, i.e., the basement membrane had degenerated and the majority of the cells exhibited signs of apoptosis, most notably chromatin condensation. Analysis of these tissues with probes that reveal intracellular acidification showed that the cells first undergo an initial acidification beginning about 6-8 h after exposure to V. fischeri. As determined by end-labeling of DNA fragments, extensive endonuclease activity was detected at approximately 16-20 h post-infection. These data provide evidence that cooperative bacteria can participate in the remodeling of host tissues through the induction of host apoptotic programs.

摘要

最近研究表明,与致病细菌的关联会在其动物宿主细胞中启动凋亡程序,据推测宿主细胞死亡是免疫系统的一种反应,要么作为宿主防御机制启动,要么作为细菌攻击的结果。在本研究中,我们提供证据表明,细菌引发的凋亡既不限于发病机制,也不限于免疫反应的启动。在乌贼Euprymna scolopes与发光细菌费氏弧菌的共生关系中,在这两种生物相互作用的最初几天里,细菌会诱导宿主组织发生显著的形态发生。最显著的变化是细菌引发的广泛浅表上皮细胞丢失,这加剧了感染过程。我们对这些组织的分析表明,细菌在与细菌相互作用的数小时内,就在构成该上皮的细胞中诱导凋亡。超微结构分析显示,24小时后上皮的完整性丧失,即基底膜退化,大多数细胞表现出凋亡迹象,最明显的是染色质浓缩。用揭示细胞内酸化的探针分析这些组织表明,细胞在接触费氏弧菌后约6-8小时开始首先经历初始酸化。通过对DNA片段进行末端标记确定,在感染后约16-20小时检测到广泛的核酸内切酶活性。这些数据提供了证据,表明共生细菌可通过诱导宿主凋亡程序参与宿主组织的重塑。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验