Maurer Jana, Hupp Sabrina, Bischoff Carolin, Foertsch Christina, Mitchell Timothy J, Chakraborty Trinad, Iliev Asparouh I
DFG Membrane/Cytoskeleton Interaction Group, Institute of Pharmacology and Toxicology & Rudolf Virchow Center for Experimental Biomedical Science, University of Würzburg, Versbacherstr. 9, 97078 Würzburg, Germany.
Institute of Physiology and Pathophysiology, Heidelberg University, Im Neuenheimer Feld 326, 69120 Heidelberg, Germany.
Toxins (Basel). 2017 Jan 13;9(1):34. doi: 10.3390/toxins9010034.
Cholesterol-dependent cytolysins (CDCs) are protein toxins that originate from Gram-positive bacteria and contribute substantially to their pathogenicity. CDCs bind membrane cholesterol and build prepores and lytic pores. Some effects of the toxins are observed in non-lytic concentrations. Two pathogens, and , cause fatal bacterial meningitis, and both produce toxins of the CDC family-pneumolysin and listeriolysin O, respectively. It has been demonstrated that pneumolysin produces dendritic varicosities (dendrite swellings) and dendritic spine collapse in the mouse neocortex, followed by synaptic loss and astrocyte cell shape remodeling without elevated cell death. We utilized primary glial cultures and acute mouse brain slices to examine the neuropathological effects of listeriolysin O and to compare it to pneumolysin with identical hemolytic activity. In cultures, listeriolysin O permeabilized cells slower than pneumolysin did but still initiated non-lytic astrocytic cell shape changes, just as pneumolysin did. In an acute brain slice culture system, listeriolysin O produced dendritic varicosities in an NMDA-dependent manner but failed to cause dendritic spine collapse and cortical astrocyte reorganization. Thus, listeriolysin O demonstrated slower cell permeabilization and milder glial cell remodeling ability than did pneumolysin and lacked dendritic spine collapse capacity but exhibited equivalent dendritic pathology.
胆固醇依赖性细胞毒素(CDCs)是源自革兰氏阳性菌的蛋白质毒素,对其致病性有重要作用。CDCs与膜胆固醇结合并形成前孔和裂解孔。在非裂解浓度下也能观察到这些毒素的一些作用。两种病原体,肺炎链球菌和单核细胞增生李斯特菌,可引发致命的细菌性脑膜炎,且分别产生CDC家族毒素——肺炎溶血素和李斯特菌溶血素O。已证明肺炎溶血素可在小鼠新皮层中产生树突膨体(树突肿胀)和树突棘塌陷,随后出现突触丧失和星形胶质细胞形态重塑,但细胞死亡并未增加。我们利用原代神经胶质细胞培养物和急性小鼠脑片来研究李斯特菌溶血素O的神经病理学作用,并将其与具有相同溶血活性的肺炎溶血素进行比较。在培养物中,李斯特菌溶血素O使细胞通透的速度比肺炎溶血素慢,但仍像肺炎溶血素一样引发非裂解性星形胶质细胞形态改变。在急性脑片培养系统中,李斯特菌溶血素O以NMDA依赖的方式产生树突膨体,但未能导致树突棘塌陷和皮质星形胶质细胞重组。因此,与肺炎溶血素相比,李斯特菌溶血素O使细胞通透的速度较慢,神经胶质细胞重塑能力较弱,缺乏树突棘塌陷能力,但表现出相当的树突病理变化。