妊娠晚期胎儿肾脏中发育中的肾元间质-显微解剖检查。

IF 2.4 Q1 PEDIATRICS
Will W Minuth
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引用次数: 1

摘要

背景:一系列损伤可引起早产儿和低出生体重儿肾元形成的终止。这导致少肾病,对晚年的健康造成严重后果。虽然临床参数已被广泛研究,但对初始损害知之甚少。既往病理表现为肾源区宽度减小,缺少s型体。目前的形态学研究表明,由于形成肾元旁边的相互模式,它的结构邻居,特别是间质,也一定受到影响。然而,除了综合和掌握功能的研究结果外,还没有系统的显微解剖学数据来解释妊娠晚期胎儿肾脏中发育中的肾元间质的结构。因此,本文阐述了典型特征。结果:生成的数据表明,祖细胞、肾源性生态位、肾小管前聚集和间质向上皮的转变仅限于包膜下间质。在随后的发育过程中,只有肾小泡的远端和逗号形和s形体与肾小泡保持进一步的接触。近端分别位于小管周围间质对面,位于下方但先前形成的肾元的连接小管处。相关的内侧面面向集合管壶腹狭窄的小管周围间质,首先是在其尖端,然后是其头部、圆锥和颈部,最后是分化的CD小管。侧面从包膜下间质开始,然后沿着邻近的上行穿通辐射动脉的宽血管周围间质。当肾元成熟时,间质结构再次改变。结论:本研究表明,胎儿肾脏形成肾元的间质由现有的、短暂的、阶段特异性的和不同程度成熟的室室组成。根据发育的需要,它通过形成、降解、融合和重建来改变其形状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The interstitium at the developing nephron in the fetal kidney during advanced pregnancy - a microanatomical inventory.

The interstitium at the developing nephron in the fetal kidney during advanced pregnancy - a microanatomical inventory.

The interstitium at the developing nephron in the fetal kidney during advanced pregnancy - a microanatomical inventory.

The interstitium at the developing nephron in the fetal kidney during advanced pregnancy - a microanatomical inventory.

Background: A series of noxae can evoke the termination of nephron formation in preterm and low birth weight babies. This results in oligonephropathy with severe consequences for health in the later life. Although the clinical parameters have been extensively investigated, little is known about the initial damage. Previous pathological findings indicate the reduction in width of the nephrogenic zone and the lack of S-shaped bodies. Current morphological investigations suggest that due to the mutual patterning beside the forming nephron, also its structural neighbors, particularly the interjacent interstitium, must be affected. However, beside the findings on integrative and mastering functions, systematic microanatomical data explaining the configuration of the interstitium at the developing nephron in the fetal kidney during advanced pregnancy is not available. Therefore, this work explains the typical features.

Results: The generated data depicts that the progenitor cells, nephrogenic niche, pretubular aggregate, and mesenchymal-to-epithelial transition are restricted to the subcapsular interstitium. During the proceeding development, only the distal pole of the renal vesicles and comma- and S-shaped bodies stays in further contact with it. The respective proximal pole is positioned opposite the peritubular interstitium at the connecting tubule of an underlying but previously formed nephron. The related medial aspect faces the narrow peritubular interstitium of a collecting duct (CD) ampulla first only at its tip, then at its head, conus, and neck, and finally at the differentiating CD tubule. The lateral aspect starts at the subcapsular interstitium, but then it is positioned along the wide perivascular interstitium of the neighboring ascending perforating radiate artery. When the nephron matures, the interstitial configuration changes again.

Conclusions: The present investigation illustrates that the interstitium at the forming nephron in the fetal kidney consists of existing, transient, stage-specific, and differently far matured compartments. According to the developmental needs, it changes its shape by formation, degradation, fusion, and rebuilding.

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