Department of Diagnostic and Interventional Radiology, University Hospital in Split, 21000 Split, Croatia.
Department of Anatomy, Histology and Embryology, School of Medicine, University of Split, 21000 Split, Croatia.
Int J Mol Sci. 2021 Jul 7;22(14):7320. doi: 10.3390/ijms22147320.
The expression of 5-HT (serotonin) receptors (sr) was analyzed in the spinal cord and ganglia of 15 human conceptuses (5-10-weeks), and in the 9-week fetus with spina bifida. We used immunohistochemical method to detect sr-positive, apoptotic (caspase-3) and proliferating (Ki-67) cells, double immunofluorescence for co-localization with protein gene peptide (pgp) 9.5 and GFAP, as well as semiquantification and statistical measurements. Following the neurulation process, moderate (sr1 and sr2) and mild (sr3) expression characterized neuroblasts in the spinal cord and ganglia. During further development, sr1 expression gradually increased in the motoneurons, autonomic and sensory neurons, while sr2 and sr3 increased strongly in floor and roof plates. In the ganglia, sr3 expression increased during limited developmental period, while sr1 and sr2 increased throughout the investigated period. Co-expression of sr/pgp 9.5 characterized developing neurons, while sr/GFAP co-localized in the roof plate. In the spinal cord and ganglia of malformed fetus, weaker sr1 and sr2 and stronger sr3 expression accompanied morphological abnormalities. Anomalous roof plate morphology showed an excess of apoptotic and proliferating cells and increased sr3 expression. Our results indicate a human-species specific sr expression pattern, and the importance of sr1 in neuronal differentiation, and sr2 and sr3 in the control of the roof plate morphogenesis in normal and disturbed development.
5-羟色胺(5-HT)受体(sr)在 15 个人类胚胎(5-10 周)脊髓和神经节以及伴有脊柱裂的 9 周胎儿中的表达进行了分析。我们使用免疫组织化学方法检测 sr 阳性、凋亡(caspase-3)和增殖(Ki-67)细胞,并用蛋白基因肽(pgp)9.5 和 GFAP 进行双重免疫荧光,以及半定量和统计测量。在神经发生过程之后,中度(sr1 和 sr2)和轻度(sr3)表达特征性地存在于脊髓和神经节中的神经母细胞。在进一步发育过程中,sr1 表达在运动神经元、自主和感觉神经元中逐渐增加,而 sr2 和 sr3 在底板和顶板中强烈增加。在神经节中,sr3 表达在有限的发育期间增加,而 sr1 和 sr2 在整个研究期间增加。sr/pgp 9.5 的共表达特征性地表达了发育中的神经元,而 sr/GFAP 共定位在顶板上。在畸形胎儿的脊髓和神经节中,较弱的 sr1 和 sr2 以及较强的 sr3 表达伴随着形态异常。异常的顶板形态显示出凋亡和增殖细胞增多以及 sr3 表达增加。我们的结果表明了一种人类特异性的 sr 表达模式,以及 sr1 在神经元分化中的重要性,以及 sr2 和 sr3 在正常和发育障碍中控制顶板形态发生中的重要性。