Behavioural Neuroscience Laboratory, Department of Animal Science, School of Life Sciences, Bharathidasan University, Tiruchirappalli, India.
Department of Biotechnology, Alagappa University, Karaikudi, India.
Dev Neurosci. 2022;44(6):547-556. doi: 10.1159/000525821. Epub 2022 Jul 7.
The purpose of this study was to examine whether the Cronobacter sakazakii infection-induced inflammation alters the Reelin signaling pathway that is involved in learning and memory. To test this, postnatal day (PND)-15 rat pups were either treated with Luria Bertani broth/Escherichia coli OP50/C. sakazakii through oral gavage or maintained as control and allowed to stay with their mothers until PND-24. Experimental groups' rats were subjected to long-term novel object recognition test during their adolescent age PND-30-32. Observed behavioral data showed that C. sakazakii infection causes a deficit in recognition of novel objects from known objects. Further, our analysis showed that C. sakazakii infection-mediated inflammation decreases the Reelin expression by proteolytic cleavage and alters its receptor apolipoprotein E-receptor (ApoER)-2 splice variants ApoER2 (ex19) and ApoER2 (Δ). Subsequently, downregulated Reelin alters the phosphorylation of disabled adapter protein (Dab)-1 and leads to differential expression of N-methyl-D-aspartate (NMDA) receptor subunits 2A and 2B. Further, the NMDA receptor influences the expression of postsynaptic density (PSD)-95 protein and brain-derived neurotrophic factor (BDNF). Observed results suggest a deficit in recognition of novel objects possibly due to the alternation in Reelin signaling pathway.
本研究旨在探讨克罗诺杆菌感染引起的炎症是否会改变参与学习和记忆的 Reelin 信号通路。为此,在产后第 15 天(PND)-15 的大鼠幼崽中,通过口服灌胃给予 Luria Bertani 肉汤/大肠杆菌 OP50/C. sakazakii,或作为对照维持并允许它们与母亲在一起直到 PND-24。实验组的大鼠在青春期 PND-30-32 期间接受了长期新物体识别测试。观察到的行为数据表明,C. sakazakii 感染导致对已知物体中新物体的识别能力下降。此外,我们的分析表明,C. sakazakii 感染介导的炎症通过蛋白水解切割降低了 Reelin 的表达,并改变了其受体载脂蛋白 E 受体(ApoER)-2 剪接变体 ApoER2(ex19)和 ApoER2(Δ)。随后,下调的 Reelin 改变了Disabled Adapter Protein(Dab)-1 的磷酸化,导致 N-甲基-D-天冬氨酸(NMDA)受体亚基 2A 和 2B 的差异表达。此外,NMDA 受体影响突触后密度(PSD)-95 蛋白和脑源性神经营养因子(BDNF)的表达。观察结果表明,新物体识别能力下降可能是由于 Reelin 信号通路的改变。