产前晚期人脊髓灰质的免疫组织化学特征

A. Dovgan, O. V. Vlasenko, O. Popadynets, A. Semenenko, I. Gunas, V. P. Bobruk
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引用次数: 0

摘要

本研究致力于研究与年龄相关的(产前)脑和脊髓重组模式的相关问题,并为预测和纠正先天性缺陷的发生提供机会。本研究旨在探讨产前晚期人脊髓灰质结构中免疫组织化学标记物表达的性质。该研究的材料包括27个胎龄在35-40周的人类胎儿的脊髓准备。在研究过程中使用了以下方法:对获得的数据进行解剖,一般组织学,特殊组织学,免疫组织化学,形态计量学和统计分析。研究发现,在妊娠35-36周时,神经干细胞(NSCs)在脊髓节段腹侧神经上皮的增殖比在背侧神经上皮的增殖更为强烈。在腹侧神经上皮,有5-6个有丝分裂或有丝分裂后的NSCs,而在背侧,只有2-3个细胞。在39-40周的胎儿中,颈和腰椎节段背神经上皮中神经干细胞的增殖活性较高,其中6%的细胞中检测到Ki-67表达(7-8个细胞有反应),而在胸和骶节段,Ki-67表达为4%(3-4个细胞有反应)。与背侧神经上皮相比,在节段神经上皮的腹侧部分,神经干细胞的增殖活性略弱。在颈椎和腰椎节段,4%的细胞表达Ki-67(3-4个细胞有反应),在胸椎和骶节段,2%的细胞表达Ki-67(1-2个细胞有反应)。在妊娠35-36周时,在神经上皮周围、后角基部和后正中隔沿线观察到高表达的波形蛋白。Vimentin在地幔层的表达相对较弱,并沿血管和脊髓根形成区持续表达。出生前,在神经上皮周围的放射状胶质残体中检测到相对较弱的波形蛋白表达。神经上皮内未见波形蛋白表达,但血管周围可见局灶性波形蛋白表达。神经上皮中波形蛋白表达缺失表明放射状细胞消失。在妊娠35-40周时,脊髓节段的套膜层突触体素表达较强,表明神经连接的建立和神经纤维的髓鞘形成的强度。这些过程在出生后继续进行。神经上皮内未见突触素表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunohistochemical characteristics of the gray matter of the human spinal cord in the late prenatal period
The study is dedicated to the relevant problem of studying the patterns of age-related (prenatal) restructuring in the brain and spinal cord and provides opportunities for predicting and correcting the occurrence of congenital defects. The aim of the research was to establish the nature of immunohistochemical marker expression in the gray matter structures of the human spinal cord during the late prenatal period. The material for the study consisted of spinal cord preparations from 27 human fetuses at gestational age 35-40 weeks. The following methods were used during the research: anatomical, general histological, special histological, immunohistochemical, morphometric, and statistical analysis of the obtained data. It was found that at 35-36 weeks of the gestational period, the proliferation of neural stem cells (NSCs) occurs more intensively in the ventral neuroepithelium of spinal cord segments compared to the dorsal neuroepithelium. In the ventral neuroepithelium, there are 5-6 mitotic or post-mitotic NSCs, while in the dorsal part, there are only 2-3 cells. In fetuses at 39-40 weeks, the proliferative activity of neural stem cells in the dorsal neuroepithelium is higher in cervical and lumbar segments, where Ki-67 expression is detected in 6 % of cells (reactive in 7-8 cells), and in thoracic and sacral segments, it is 4 % (reactive in 3-4 cells). In contrast to the dorsal neuroepithelium, in the ventral part of the neuroepithelium of the segments, the proliferative activity of neural stem cells is slightly less intense. In cervical and lumbar segments, Ki-67 expression occurred in 4 % of cells (reactive in 3-4 cells), and in thoracic and sacral segments, it was 2 % (reactive in 1-2 cells). At 35-36 weeks of gestation, high vimentin expression was observed around the neuroepithelium, at the base of the posterior horns, and along the posterior median septum. Vimentin expression in the mantle layer was relatively weak and persisted along blood vessels and in the area of spinal cord root formation. Before birth, relatively weak vimentin expression was detected in the remnants of radial glia surrounding the neuroepithelial layer. Vimentin expression was absent in the neuroepithelium proper, but focal vimentin expression was observed around blood vessels. The absence of vimentin expression in the neuroepithelium indicates the disappearance of radial cells. At 35-40 weeks of the gestational period, relatively strong synaptophysin expression was observed in the mantle layer of spinal cord segments, indicating the intensity of neuronal connectivity establishment and myelination of nerve fibers. These processes continue after birth. Synaptophysin expression was absent in the neuroepithelium proper.
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