Ghibaudi Marco, Marchetti Nicole, Vergnano Elena, La Rosa Chiara, Benedetti Bruno, Couillard-Despres Sebastien, Farioli-Vecchioli Stefano, Bonfanti Luca
Neuroscience Institute Cavalieri Ottolenghi (NICO), Orbassano, Italy.
Department of Veterinary Sciences, University of Turin, Turin, Italy.
Front Cell Neurosci. 2023 Jul 28;17:1205173. doi: 10.3389/fncel.2023.1205173. eCollection 2023.
The recent identification of a population of non-newly born, prenatally generated "immature" neurons in the layer II of the piriform cortex (cortical immature neurons, cINs), raises questions concerning their maintenance or depletion through the lifespan. Most forms of brain structural plasticity progressively decline with age, a feature that is particularly prominent in adult neurogenesis, due to stem cell depletion. By contrast, the entire population of the cINs is produced during embryogenesis. Then these cells simply retain immaturity in postnatal and adult stages, until they "awake" to complete their maturation and ultimately integrate into neural circuits. Hence, the question remains open whether the cINs, which are not dependent on stem cell division, might follow a similar pattern of age-related reduction, or in alternative, might leave a reservoir of young, undifferentiated cells in the adult and aging brain. Here, the number and features of cINs were analyzed in the mouse piriform cortex from postnatal to advanced ages, by using immunocytochemistry for the cytoskeletal marker doublecortin. The abundance and stage of maturation of cINs, along with the expression of other markers of maturity/immaturity were investigated. Despite a marked decrease in this neuronal population during juvenile stages, reminiscent of that observed in hippocampal neurogenesis, a small amount of highly immature cINs persisted up to advanced ages. Overall, albeit reducing in number with increasing age, we report that the cINs are present through the entire animal lifespan.
最近在梨状皮层II层中发现了一群并非新生的、产前生成的“未成熟”神经元(皮层未成熟神经元,cINs),这引发了关于它们在整个生命周期中是如何维持或消耗的问题。大多数形式的脑结构可塑性会随着年龄的增长而逐渐下降,这一特征在成体神经发生中尤为突出,原因是干细胞耗竭。相比之下,cINs的整个群体是在胚胎发生过程中产生的。然后这些细胞在出生后和成年阶段简单地保持未成熟状态,直到它们“觉醒”以完成成熟并最终整合到神经回路中。因此,问题仍然存在:不依赖干细胞分裂的cINs是否可能遵循类似的与年龄相关的减少模式,或者,是否可能在成年和衰老大脑中留下年轻的、未分化细胞的储备。在这里,通过使用细胞骨架标记物双皮质素的免疫细胞化学方法,分析了从出生后到老年小鼠梨状皮层中cINs的数量和特征。研究了cINs的丰度和成熟阶段,以及其他成熟/未成熟标记物的表达。尽管在幼年阶段这群神经元数量显著减少,这让人想起在海马神经发生中观察到的情况,但少量高度未成熟的cINs一直持续到老年。总体而言,尽管随着年龄的增长数量减少,但我们报告称cINs在整个动物生命周期中都存在。