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Astrocytes Enhance Streptococcus suis -Glial Cell Interaction in Primary Astrocyte-Microglial Cell Co-Cultures

机译:星形胶质细胞增强猪链球菌-胶质细胞在原代星形胶质细胞-小胶质细胞共培养物中的相互作用

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Streptococcus ( S .) suis infections are the most common cause of meningitis in pigs. Moreover, S. suis is a zoonotic pathogen, which can lead to meningitis in humans, mainly in adults. We assume that glial cells may play a crucial role in host-pathogen interactions during S. suis infection of the central nervous system. Glial cells are considered to possess important functions during inflammation and injury of the brain in bacterial meningitis. In the present study, we established primary astrocyte-microglial cell co-cultures to investigate interactions of S. suis with glial cells. For this purpose, microglial cells and astrocytes were isolated from new-born mouse brains and characterized by flow cytometry, followed by the establishment of astrocyte and microglial cell mono-cultures as well as astrocyte-microglial cell co-cultures. In addition, we prepared microglial cell mono-cultures co-incubated with uninfected astrocyte mono-culture supernatants and astrocyte mono-cultures co-incubated with uninfected microglial cell mono-culture supernatants. After infection of the different cell cultures with S. suis , bacteria-cell association was mainly observed with microglial cells and most prominently with a non-encapsulated mutant of S. suis . A time-dependent induction of NO release was found only in the co-cultures and after co-incubation of microglial cells with uninfected supernatants of astrocyte mono-cultures mainly after infection with the capsular mutant. Only moderate cytotoxic effects were found in co-cultured glial cells after infection with S. suis . Taken together, astrocytes and astrocyte supernatants increased interaction of microglial cells with S. suis . Astrocyte-microglial cell co-cultures are suitable to study S. suis infections and bacteria-cell association as well as NO release by microglial cells was enhanced in the presence of astrocytes.
机译:猪链球菌感染是猪脑膜炎的最常见原因。此外,猪链球菌是一种人畜共患病原体,可导致人类(主要是成年人)脑膜炎。我们假设神经胶质细胞可能在猪链球菌感染中枢神经系统期间在宿主与病原体的相互作用中起关键作用。在细菌性脑膜炎的脑部炎症和损伤期间,胶质细胞被认为具有重要的功能。在本研究中,我们建立了原代星形胶质细胞-小胶质细胞共培养物,以研究猪链球菌与神经胶质细胞的相互作用。为此,从新生小鼠大脑中分离出小胶质细胞和星形胶质细胞,并通过流式细胞仪进行表征,然后建立星形胶质细胞和小胶质细胞单培养物以及星形胶质细胞-小胶质细胞共培养物。此外,我们准备了与未感染的星形胶质细胞单培养上清液共孵育的小胶质细胞单培养物和与未感染的微胶质细胞单培养上清液共孵育的星形胶质细胞单培养物。在猪链球菌感染不同的细胞培养物后,细菌-细胞结合主要观察到小胶质细胞,最显着的是未封装的猪链球菌突变体。仅在共培养物中以及主要在被荚膜突变体感染后,将小胶质细胞与未感染的星形胶质细胞单培养物的上清液共孵育后,发现NO的释放具有时间依赖性。猪链球菌感染后,在共培养的神经胶质细胞中仅发现中等程度的细胞毒性作用。总之,星形胶质细胞和星形胶质细胞上清液增加了小胶质细胞与猪链球菌的相互作用。星形胶质细胞-小胶质细胞共培养物适合研究猪链球菌感染和细菌-细胞缔合以及在星形胶质细胞存在下小胶质细胞释放NO的作用增强。

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