Centre for Integrated Systems Biology & Medicine, School of Biomedical Sciences, Queen's Medical Centre, University of Nottingham, UK.
J Anat. 2009 Jul;215(1):77-90. doi: 10.1111/j.1469-7580.2008.00994.x. Epub 2008 Jan 2.
Stereology applied to randomly-generated thin sections allows minimally-biased and economical quantitation of the 3D structure of the placenta from molecular to whole-organ levels. With these sampling and estimation tools, it is possible to derive global quantities (tissue volumes, interface surface areas, tubule lengths and particle numbers), average values (e.g. mean cell size or membrane thickness), spatial relationships (e.g. between compartments and immunoprobes) and functional potential (e.g. diffusive conductance). This review indicates ways in which stereology has been used to interpret the morphology of human and murine placentas including the processes of villous growth, trophoblast differentiation, vascular morphogenesis and diffusive transport. In human placenta, global quantities have shown that villous maturation involves differential growth of fetal capillaries and increases in endothelial cell number. Villous trophoblast is a continuously renewing epithelium and, through much of gestation, exhibits a steady state between increasing numbers of nuclei in cytotrophoblast (CT) and syncytiotrophoblast (ST). The epithelium gradually becomes thinner because its surface expands at a faster rate than its volume. These changes help to ensure that placental diffusing capacity matches the growth in fetal mass. Comparable events occur in the murine placenta. Some of these processes are perturbed in complicated pregnancies: 1) fetoplacental vascular growth is compromised in pregnancies accompanied by maternal asthma, 2) changes in trophoblast turnover occur in pre-eclampsia and intrauterine growth restriction, and 3) uteroplacental vascular development is impoverished, but diffusive transport increases, in pregnant mice exposed to particulate urban air pollution. Finally, quantitative immunoelectron microscopy now permits more rigorous analysis of the spatial distributions of interesting molecules between subcellular compartments or shifts in distributions following experimental manipulation.
体视学应用于随机生成的薄片允许从分子到整个器官水平对胎盘的 3D 结构进行最小偏倚和经济的定量。有了这些采样和估计工具,可以得出全局数量(组织体积、界面表面积、小管长度和颗粒数量)、平均值(例如平均细胞大小或膜厚度)、空间关系(例如隔室之间和免疫探针之间)和功能潜力(例如扩散电导)。这篇综述表明了体视学如何用于解释人类和鼠类胎盘的形态,包括绒毛生长、滋养层分化、血管形态发生和扩散运输过程。在人类胎盘,全局数量表明,绒毛成熟涉及胎儿毛细血管的差异生长和内皮细胞数量的增加。绒毛滋养层是一个不断更新的上皮组织,在妊娠的大部分时间内,在滋养层细胞(CT)和合体滋养层(ST)中核数的增加之间表现出稳定状态。上皮组织逐渐变薄,因为其表面积的扩张速度快于其体积。这些变化有助于确保胎盘的扩散能力与胎儿体重的增长相匹配。类似的事件也发生在鼠类胎盘。一些复杂的妊娠会干扰这些过程:1)母体哮喘伴随的胎儿胎盘血管生长受损,2)子痫前期和宫内生长受限出现滋养层周转率变化,3)暴露于颗粒状城市空气污染的妊娠小鼠的子宫胎盘血管发育不良,但扩散运输增加。最后,定量免疫电子显微镜现在允许更严格地分析亚细胞隔室之间感兴趣分子的空间分布或实验处理后分布的变化。