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通过微计算机断层扫描评估心脏形态发生的定量容积分析。

Quantitative volumetric analysis of cardiac morphogenesis assessed through micro-computed tomography.

作者信息

Butcher Jonathan T, Sedmera David, Guldberg Robert E, Markwald Roger R

机构信息

Cardiovascular Developmental Biology Center, Department of Cell Biology and Anatomy, Medical University of South Carolina, Charleston, SC 29425, USA.

出版信息

Dev Dyn. 2007 Mar;236(3):802-9. doi: 10.1002/dvdy.20962.

Abstract

We present a method to generate quantitative embryonic cardiovascular volumes at extremely high resolution without tissue shrinkage using micro-computed tomography (Micro-CT). A CT dense polymer (Microfil, Flow Tech, Inc.) was used to perfuse avian embryonic hearts from Hamburger and Hamilton stage (HH) 15 through HH36, which solidified to create a cast within the luminal space. Hearts were then scanned at 10.5 mum(3) voxel resolution using a VivaCT scanner, digital slices were contoured for regions of interest, and computational analysis was conducted to quantify morphogenetic parameters. The three-dimensional morphology was compared with that of scanning electron microscopy (SEM) images and serial section reconstruction of similarly staged hearts. We report that Microfil-perfused hearts swelled to maximum end-diastolic volume with negligible shrinking after polymerization. Comparison to SEM revealed good agreement of cardiac chamber proportions and intracardiac tissue structures (i.e., valves and septa) at the stages of development assessed. Quantification of changes in chamber volume over development revealed several notable results that confirm earlier hypotheses. Heart chamber volumes grow over two orders of magnitude during the 1-week developmental period analyzed. The atrioventricular canal comprised a significant proportion of the early heart volume. While left atrium/left ventricular volume ratios approached 1 in later development, right atrium/right ventricle ratios increase to over 2.5. Quantification of trabeculation patterns confirmed that the right and left ventricles are similarly trabeculated before HH27, after which the right ventricle became quantitatively coarser than that of the left ventricle. These results demonstrate that Micro-CT can be used to image and quantify cardiovascular structures during development.

摘要

我们提出了一种使用微计算机断层扫描(Micro-CT)在不发生组织收缩的情况下以极高分辨率生成定量胚胎心血管容积的方法。一种CT致密聚合物(Microfil,Flow Tech公司)用于从汉伯格和汉密尔顿分期(HH)15到HH36灌注禽胚胎心脏,该聚合物凝固后在管腔空间内形成铸型。然后使用VivaCT扫描仪以10.5立方微米的体素分辨率对心脏进行扫描,对感兴趣区域的数字切片进行轮廓描绘,并进行计算分析以量化形态发生参数。将三维形态与扫描电子显微镜(SEM)图像以及相似分期心脏的连续切片重建结果进行比较。我们报告称,用Microfil灌注的心脏在聚合后膨胀至最大舒张末期容积,收缩可忽略不计。与SEM的比较显示,在所评估的发育阶段,心腔比例和心内组织结构(即瓣膜和隔膜)具有良好的一致性。对发育过程中心腔容积变化的量化揭示了几个显著结果,证实了早期的假设。在所分析的1周发育期间,心腔容积增长超过两个数量级。房室管在早期心脏容积中占很大比例。虽然左心房/左心室容积比在后期发育中接近1,但右心房/右心室比增加到超过2.5。对小梁模式的量化证实,在HH27之前,右心室和左心室的小梁化程度相似,之后右心室在数量上比左心室更粗糙。这些结果表明,Micro-CT可用于在发育过程中对心血管结构进行成像和量化。

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