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新生仓鼠大脑半球内侧脑膜细胞的破坏会阻止齿状回锥体下叶片的形成。

Destruction of meningeal cells over the medial cerebral hemisphere of newborn hamsters prevents the formation of the infrapyramidal blade of the dentate gyrus.

作者信息

Hartmann D, Sievers J, Pehlemann F W, Berry M

机构信息

Anatomisches Institut, Universität Kiel, Federal Republic of Germany.

出版信息

J Comp Neurol. 1992 Jun 1;320(1):33-61. doi: 10.1002/cne.903200103.

Abstract

Meningeal cells participate in the development of the cerebellum both by stabilizing the extracellular matrix of the pial surface and by organizing the radial glial scaffold and the lamination of the cerebellar cortex. In the present study we investigated possible influences of meningeal cells on the development of the dentate gyrus, whose ontogenesis has many similarities to that of the cerebellum. Meningeal cells were selectively destroyed by injecting newborn hamsters with 25 micrograms 6-hydroxydopamine (6-OHDA) into the interhemispheric fissure. Twenty-four hours postinjection (p.i.) the meningeal cells over the medial cerebral hemispheres were completely destroyed. Thirty days p.i. the infrapyramidal blade of the dentate gyrus was almost completely missing, while the suprapyramidal blade was hypertrophied, extending with its medial tip almost up to the medial surface of the cortex. In order to ascertain that this maldevelopment was caused by the destruction of meningeal cells, another group of hamsters was pretreated with normetanephrine (NMN) which inhibits the extraneuronal uptake of 6-OHDA into meningeal cells. In this group the meningeal cells were unaffected by the treatment, and the morphology of the dentate gyrus was normal 30 days p.i. of 6-OHDA plus NMN. When the meningeal cells were destroyed in later stages of development (postnatal days 1-5), alterations of the dentate gyrus could be induced only up to the fourth postnatal day; thereafter, 6-OHDA treatment left it unchanged. This indicates a critical period of meningeal cell influence that coincides with the period of existence of the subpial dentate matrix. Analysis of the time course of the defective development revealed that in the first 5 days p.i. 1) meningeal cells over the medial cerebral hemisphere were destroyed and removed, 2) the pial basement membrane over both the dentate anlage and the diencephalon thinned and ruptured, and the adjacent brain parts fused focally, 3) many cells of the subpial dentate matrix disappeared from their subsurface position, 4) the number of "immature" cells increased in the hilus and the subgranular zone of the suprapyramidal blade, 5) the suprapyramidal blade elongated and thickened considerably, while the infrapyramidal blade did not form. Beyond 5 days p.i. those parts of the pial surface of the dentate anlage that had not fused with the diencephalon were repopulated with meningeal cells. This reappearance of meningeal cells was accompanied by 1) the restitution of the normal morphology of the basement membrane, 2) the reappearance of neuronal and glial cells below the pial surface, and 3) the formation of fragments of the infrapyramidal blade which later developed a normal appearing lamination.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

脑膜细胞通过稳定软膜表面的细胞外基质以及组织放射状胶质支架和小脑皮质的分层来参与小脑的发育。在本研究中,我们调查了脑膜细胞对齿状回发育可能产生的影响,齿状回的个体发生与小脑有许多相似之处。通过向新生仓鼠的大脑半球间裂注射25微克6 - 羟基多巴胺(6 - OHDA)来选择性破坏脑膜细胞。注射后24小时,大脑半球内侧的脑膜细胞被完全破坏。注射后30天,齿状回的锥体下叶片几乎完全缺失,而锥体上叶片肥大,其内侧尖端几乎延伸至皮质的内侧表面。为了确定这种发育异常是由脑膜细胞的破坏引起的,另一组仓鼠用去甲变肾上腺素(NMN)进行预处理,NMN可抑制6 - OHDA进入脑膜细胞的非神经元摄取。在这组中,脑膜细胞未受该处理影响,在注射6 - OHDA加NMN后30天,齿状回的形态正常。当在发育后期(出生后1 - 5天)破坏脑膜细胞时,齿状回的改变仅在出生后第四天之前可被诱导;此后,6 - OHDA处理对其没有影响。这表明脑膜细胞影响的关键期与软膜下齿状基质存在的时期一致。对发育缺陷的时间进程分析表明,在注射后的前5天:1)大脑半球内侧的脑膜细胞被破坏并清除;2)齿状原基和间脑上方的软膜基底膜变薄并破裂,相邻脑区局部融合;3)许多软膜下齿状基质细胞从其表面下位置消失;4)锥体上叶片的齿状回门和颗粒下区“未成熟”细胞数量增加;5)锥体上叶片显著伸长和增厚,而锥体下叶片未形成。注射后5天以上,齿状原基软膜表面未与间脑融合的部分重新出现脑膜细胞。脑膜细胞的这种重新出现伴随着:1)基底膜正常形态的恢复;2)软膜表面下神经元和胶质细胞的重新出现;3)锥体下叶片碎片的形成,这些碎片后来发育出正常的分层结构。(摘要截断于400字)

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