Pardillo-Díaz Ricardo, Pérez-García Patricia, Ortego-Domínguez María, Gómez-Oliva Ricardo, Martínez-Gómez Nora, Domínguez-García Samuel, García-Cózar Francisco, Muñoz-Miranda Juan Pedro, Hernández-Galán Rosario, Carrascal Livia, Castro Carmen, Nunez-Abades Pedro
Department of Physiology, University of Seville, Seville, Spain.
Division of Physiology, University of Cadiz, Cadiz, Spain.
Stem Cell Res Ther. 2025 Jan 5;16(1):1. doi: 10.1186/s13287-024-04105-4.
Neural stem cells from the subventricular zone (SVZ) neurogenic niche provide neurons that integrate in the olfactory bulb circuitry. However, in response to cortical injuries, the neurogenic activity of the SVZ is significantly altered, leading to increased number of neuroblasts with a modified migration pattern that leads cells towards the site of injury. Despite the increased neurogenesis and migration, many newly generated neurons fail to survive or functionally integrate into the cortical circuitry. Providing the injured area with the adequate signaling molecules may improve both migration and functional integration of newly generated neurons.
In here, we have studied the effect of a diterpene with the capacity to induce neuregulin release at promoting neurogenesis in a murine model of cortical brain injury. Using green fluorescent protein expressing vectors we have labeled SVZ cells and have studied the migration of newly generated neuroblasts toward the injury in response the treatment. In addition, using electrophysiological recordings we have studied the differentiation of these neuroblasts into mature neurons and their functional integration into the cortical circuitry. We have studied their electrical properties, their morphology and cortical location.
We have found that EOF2 treatment of adult mice with mechanical cortical injuries facilitates the delivery of neuroblasts into these injuries. The newly generated neurons develop features of fully functional neurons. Our results show that the newly generated neurons receive electrical inputs, fire action potentials, and undergo complete differentiation into neurons recapitulating the stages that distinguish ontogenic differentiation. These neurons develop features representative of neurons belonging the cortical layer in which they are situated. We have also studied that EOF2 facilitates neuregulin release in SVZ cells, a signaling factor that promotes neuronal differentiation. Neuregulin is expressed in microglial cells that reach the injury in response to the damage and its release is increased by EOF2 treatment.
Promoting neuregulin release via diterpene treatment facilitates migration of SVZ-derived neuroblasts to cortical injuries stimulating their differentiation into mature functional neurons, which receive electrical inputs and develop features of cortical neurons. These findings highlight the role of diterpenoids as a potential therapy to repair cortical brain injuries.
来自脑室下区(SVZ)神经源性微环境的神经干细胞可提供整合到嗅球回路中的神经元。然而,在应对皮质损伤时,SVZ的神经发生活动会显著改变,导致神经母细胞数量增加,其迁移模式也发生改变,使细胞趋向损伤部位。尽管神经发生和迁移有所增加,但许多新生成的神经元无法存活或在功能上整合到皮质回路中。为损伤区域提供适当的信号分子可能会改善新生成神经元的迁移和功能整合。
在此,我们研究了一种具有诱导神经调节蛋白释放能力的二萜在促进皮质脑损伤小鼠模型神经发生中的作用。使用表达绿色荧光蛋白的载体标记SVZ细胞,并研究了新生成的神经母细胞在治疗后向损伤部位的迁移。此外,通过电生理记录,我们研究了这些神经母细胞向成熟神经元的分化及其在皮质回路中的功能整合。我们研究了它们的电特性、形态和皮质定位。
我们发现,用EOF2处理机械性皮质损伤的成年小鼠,可促进神经母细胞向这些损伤部位的输送。新生成的神经元具有完全功能性神经元的特征。我们的结果表明,新生成的神经元接收电输入、产生动作电位,并经历完全分化为神经元的过程,重现了区分个体发育分化的阶段。这些神经元具有它们所处皮质层中神经元的代表性特征。我们还研究发现,EOF2促进SVZ细胞中神经调节蛋白的释放,神经调节蛋白是一种促进神经元分化的信号因子。神经调节蛋白在响应损伤而到达损伤部位的小胶质细胞中表达,EOF2处理可增加其释放。
通过二萜处理促进神经调节蛋白的释放,可促进SVZ衍生的神经母细胞向皮质损伤部位迁移,刺激它们分化为成熟的功能性神经元,这些神经元接收电输入并具有皮质神经元的特征。这些发现突出了二萜类化合物作为修复皮质脑损伤潜在疗法的作用。