Department of Otolaryngology-HNS Wayne State University School of Medicine Detroit, Michigan, 48201, USA.
Sci Rep. 2017 Oct 23;7(1):13843. doi: 10.1038/s41598-017-13764-8.
Integration of stem cell-derived cells into native cellular environment remains a challenge in the field. This study developed novel methods to co-culture neural stem cell-derived spiral ganglion-like neurons (ScNs) and mouse auditory cochlear nucleus (CN) neurons to understand whether ScNs of the peripheral nervous system (PNS) synapse with CN neurons of the central nervous system (CNS). ScNs were obtained from neural stem cells that were derived from transgenic mouse pre-labeled with enhanced green fluorescent protein (EGFP), whereas CN neurons were from postnatal mouse primary cultures. ScNs and CN neurons were co-cultured for 4-6 days in the absence or presence of astrocyte-conditioned medium (ACM). Class III β-tubulin (TUJ1)-expressing connections were found between ScNs and CN neurons. Expression of the synaptic vesicle marker SV2 was significantly increased along connections between ScNs and CN neurons in the presence of ACM. Immunodepletion and knockout studies indicated that thrombospodin-1 played an important role in ACM-exerted synaptogenic effects. Newly-generated synapse-like structures expressed glutamatergic marker VGluT1, pre- and post-synaptic proteins. Synaptic vesicle recycling studies suggested functional synaptic vesicle retrieval. These results reveal that stem cell-derived PNS neurons are able to form functional connections with native CNS neurons, which is critical for stem cell-based neural pathway regeneration.
将干细胞衍生的细胞整合到天然细胞环境中仍然是该领域的一个挑战。本研究开发了新的方法来共培养神经干细胞衍生的螺旋神经节样神经元(ScN)和小鼠听觉蜗神经核(CN)神经元,以了解周围神经系统(PNS)的 ScN 是否与中枢神经系统(CNS)的 CN 神经元形成突触。ScN 来自用增强型绿色荧光蛋白(EGFP)预先标记的转基因小鼠的神经干细胞,而 CN 神经元来自新生小鼠的原代培养物。ScN 和 CN 神经元在不存在或存在星形胶质细胞条件培养基(ACM)的情况下共培养 4-6 天。在 ScN 和 CN 神经元之间发现了表达 III 类β-微管蛋白(TUJ1)的连接。在 ACM 的存在下,SV2 突触小泡标志物的表达沿 ScN 和 CN 神经元之间的连接显著增加。免疫耗竭和敲除研究表明,血栓调节蛋白-1在 ACM 发挥的促突触形成效应中起着重要作用。新生成的突触样结构表达谷氨酸能标记物 VGluT1、突触前和突触后蛋白。突触小泡回收研究表明功能突触小泡回收。这些结果表明,干细胞衍生的 PNS 神经元能够与天然 CNS 神经元形成功能性连接,这对于基于干细胞的神经通路再生至关重要。