Hibernation induces changes in the metacerebral neurons of Cornu aspersum: distribution and co-localization of cytoskeletal and calcium-binding proteins.

Q4 Neuroscience
Giacomo Gattoni, Violetta Insolia, Graziella Bernocchi
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引用次数: 4

Abstract

Pulmonate gastropods provide unique opportunities to examine physiological and biochemical adaptation strategies when cellular metabolic activity is reduced. In this study, cytochemical changes in metacerebral neurons of the cerebral ganglia were investigated in the garden snail Cornu aspersum during the hibernation phase. The immunocytochemical expression of three cytoskeletal markers: microtubule-associate protein 2-like (MAP-2-li), phosphorylated form of tau-like (P-Tau-li) and heavy subunit of neurofilaments-like (NF-H-li), and of two calcium-binding proteins: calmodulin-like (CaM-li) and parvalbumin-like (PV-li) was compared in active and hibernated snails. The immunopositivity for all the markers increased during hibernation versus activity in metacerebral neurons, with the notable exception of PV-li, which remained highly expressed during the whole annual cycle. Strongly positive aggregates of MAP-2-li and P-Tau-li were detected in the somata of hibernated snail neurons. P-Tau-li aggregates co-localized with CaM-li-labelled masses during hibernation. In addition, increased labelling of NF-H-li epitopes was associated with enhancement of CaM immunopositivity. These changes may reflect neural plasticity mechanisms mainly mediated by microtubule-associated proteins and CaM. Moreover, neuroprotective strategies may allow neurons to endure the prolonged hypometabolic conditions, taking into account that many of the functions controlled by the metacerebrum, such as feeding and movement, are suspended during hibernation. In this context, the molluscan ganglia model offers an easy opportunity to understand the molecular mechanisms behind these life cycle changes in cell physiology and to investigate possible cytological similarities among distantly related animals that adapt to the same environmental challenges through hibernation.

冬眠诱导角鼠脑后神经元的变化:细胞骨架蛋白和钙结合蛋白的分布和共定位。
当细胞代谢活动减少时,肺腹足类动物提供了独特的机会来检查生理和生化适应策略。本研究研究了田螺在冬眠期大脑神经节中脑神经元的细胞化学变化。比较了三种细胞骨架标记物的免疫细胞化学表达:微管相关蛋白2样(MAP-2-li)、磷酸化形式的tau样(P-Tau-li)和神经丝样重亚基(NF-H-li),以及两种钙结合蛋白:钙调素样(CaM-li)和小白蛋白样(PV-li)。在冬眠期间,所有标记物的免疫阳性程度都高于脑神经细胞的活性,但PV-li除外,它在整个年周期内保持高表达。在冬眠的蜗牛神经元体细胞中检测到MAP-2-li和P-Tau-li的强阳性聚集。冬眠期间P-Tau-li聚集体与cam -li标记的团块共定位。此外,NF-H-li表位标记的增加与CaM免疫阳性的增强有关。这些变化可能反映了主要由微管相关蛋白和CaM介导的神经可塑性机制。此外,神经保护策略可能允许神经元忍受长时间的低代谢条件,考虑到许多由中脑控制的功能,如进食和运动,在冬眠期间暂停。在这种情况下,软体动物神经节模型提供了一个简单的机会来理解这些细胞生理学生命周期变化背后的分子机制,并研究通过冬眠适应相同环境挑战的远亲动物之间可能的细胞学相似性。
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来源期刊
Invertebrate Neuroscience
Invertebrate Neuroscience NEUROSCIENCES-
自引率
0.00%
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0
审稿时长
>12 weeks
期刊介绍: Invertebrate Neurosciences publishes peer-reviewed original articles, reviews and technical reports describing recent advances in the field of invertebrate neuroscience. The journal reports on research that exploits the simplicity and experimental tractability of the invertebrate preparations to underpin fundamental advances in neuroscience. Articles published in Invertebrate Neurosciences serve to highlight properties of signalling in the invertebrate nervous system that may be exploited in the field of antiparisitics, molluscicides and insecticides. Aspects of particular interest include: Functional analysis of the invertebrate nervous system; Molecular neuropharmacology and toxicology; Neurogenetics and genomics; Functional anatomy; Neurodevelopment; Neuronal networks; Molecular and cellular mechanisms of behavior and behavioural plasticity.
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