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胚胎肺血管形成的定性和定量分析。

Qualitative and quantitative analysis of embryonic pulmonary vessel formation.

作者信息

Schachtner S K, Wang Y, Scott Baldwin H

机构信息

Children's Hospital of Philadelphia, Division of Pediatric Cardiology, Philadelphia, Pennsylvania 19104-4318, USA.

出版信息

Am J Respir Cell Mol Biol. 2000 Feb;22(2):157-65. doi: 10.1165/ajrcmb.22.2.3766.

Abstract

Vessel formation in the lung has been described as occurring by two mechanisms: proximal, or branch, pulmonary arteries develop via angiogenesis; and distal, smaller vessels form by vasculogenesis. Connections between the proximal and distal vessels establish the final vascular network. The preponderance of vessel formation has been suspected to occur during the canalicular stage of lung development. To test these hypotheses, reporter gene expression under control of the regulatory domain of fetal liver kinase-1 (flk), an early endothelial cell-specific marker, was used to evaluate mouse lungs from embryonic day 10.5 (E10.5) through 2 wk postnatal age. Morphologic assessment was performed after histochemical staining, and quantification of vessel development by a chemiluminescent assay was compared with overall embryonic lung growth. LacZ expression under flk promoter control allowed: (1) early identification of differentiating endothelial cells of the branch pulmonary arteries; (2) visualization of distal vessels forming in the lung mesenchyme (primary capillary network) with subsequent remodeling; (3) recognition of early continuity between proximal and distal vessels, occurring by E10.5; and (4) assessment of developing pulmonary veins and venous confluence. Quantitative analysis revealed increased flk regulated beta-galactosidase (beta-gal) activity of 12 ng beta-gal/lung at E12.5 to 3,215 ng beta-gal/lung at 2 wk, which corresponded to overall lung growth during this period as shown by an increase in total protein content per lung from 35 microg at E12.5 to 6,456 microg at 2 wk after birth. We identified endothelial cell precursors of the developing pulmonary vasculature before vessel lumen formation. Continuity between the proximal pulmonary artery and vessels forming in the distal mesenchyme was present even at the earliest stage evaluated, suggesting endothelial cell differentiation at the site of vessel formation (i.e., vasculogenesis) as occurs with development of the aorta. Finally, we demonstrated that lung vessel development was not accentuated during the canalicular stage, but occurred at all stages and directly corresponded to overall lung growth.

摘要

肺血管形成被描述为通过两种机制发生

近端或分支肺动脉通过血管生成发育;远端较小的血管通过血管发生形成。近端和远端血管之间的连接建立了最终的血管网络。人们怀疑血管形成的主要过程发生在肺发育的小管期。为了验证这些假设,利用受胎儿肝激酶-1(flk)调控域控制的报告基因表达,flk是一种早期内皮细胞特异性标志物,用于评估从胚胎第10.5天(E10.5)到出生后2周龄的小鼠肺。组织化学染色后进行形态学评估,并将通过化学发光测定法对血管发育的定量与整体胚胎肺生长进行比较。flk启动子控制下的LacZ表达允许:(1)早期识别分支肺动脉中正在分化的内皮细胞;(2)可视化肺间充质中形成的远端血管(初级毛细血管网络)及其随后的重塑;(3)识别近端和远端血管之间在E10.5时出现的早期连续性;(4)评估发育中的肺静脉和静脉汇合情况。定量分析显示,flk调控的β-半乳糖苷酶(β-gal)活性从E12.5时的12 ng β-gal/肺增加到2周时的3215 ng β-gal/肺,这与同期肺的整体生长相对应,如每肺总蛋白含量从E12.5时的35 μg增加到出生后2周时的6456 μg所示。我们在血管腔形成之前就鉴定出了发育中的肺血管系统的内皮细胞前体。即使在评估的最早阶段,近端肺动脉与远端间充质中形成的血管之间也存在连续性,这表明血管形成部位(即血管发生)的内皮细胞分化,就像主动脉发育时那样。最后,我们证明肺血管发育在小管期并未加速,而是在所有阶段都发生,并且与肺的整体生长直接相关。

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