Invariance of Mitochondria and Synapses in the Primary Visual Cortex of Mammals Provides Insight Into Energetics and Function

IF 2.3 4区 医学 Q3 NEUROSCIENCES
Molly T. Karl, Young Do Kim, Kavita Rajendran, Paul R. Manger, Chet C. Sherwood
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Abstract

The cerebral cortex accounts for substantial energy expenditure, primarily driven by the metabolic demands of synaptic signaling. Mitochondria, the organelles responsible for generating cellular energy, play a crucial role in this process. We investigated ultrastructural characteristics of the primary visual cortex in 18 phylogenetically diverse mammals, spanning a broad range of brain sizes from mouse to elephant. Our findings reveal remarkable uniformity in synapse density, postsynaptic density (PSD) length, and mitochondria density, indicating functional and metabolic constraints that maintain these fundamental features. Notably, we observed an average of 1.9 mitochondria per synapse across mammalian species. When considered together with the trend of decreasing neuron density with larger brain size, we find that brain enlargement in mammals is characterized by increasing proportions of synapses and mitochondria per cortical neuron. These results shed light on the adaptive mechanisms and metabolic dynamics that govern cortical ultrastructure across mammals.

Abstract Image

哺乳动物初级视觉皮层线粒体和突触的不变性为了解能量学和功能提供了启示
大脑皮层的能量消耗很大,主要由突触信号的代谢需求驱动。线粒体是负责产生细胞能量的细胞器,在这一过程中起着至关重要的作用。我们研究了 18 种不同系统发育哺乳动物初级视觉皮层的超微结构特征,这些哺乳动物的大脑大小跨度很大,从小鼠到大象都有。我们的发现揭示了突触密度、突触后密度(PSD)长度和线粒体密度的明显一致性,表明维持这些基本特征的功能和代谢限制。值得注意的是,我们观察到哺乳动物物种的每个突触平均有 1.9 个线粒体。结合神经元密度随大脑体积增大而降低的趋势,我们发现哺乳动物大脑增大的特点是每个皮层神经元的突触和线粒体比例不断增加。这些结果揭示了哺乳动物大脑皮层超微结构的适应机制和代谢动态。
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来源期刊
CiteScore
5.80
自引率
8.00%
发文量
158
审稿时长
3-6 weeks
期刊介绍: Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states. Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se. JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.
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