Department of Tissue Morphogenesis, Faculty of Medicine, Max Planck Institute for Molecular Biomedicine, University of Münster, Münster, Germany.
Nat Protoc. 2010 Sep;5(9):1518-34. doi: 10.1038/nprot.2010.113. Epub 2010 Aug 12.
The retina is a powerful experimental system for the analysis of angiogenic blood vessel growth in the postnatal organisms. The three-dimensional architecture of the vessel network and processes as diverse as endothelial cell (EC) proliferation, sprouting, perivascular cell recruitment, vessel remodeling or maturation can be investigated at high resolution. The characterization of physiological and pathological angiogenic processes in mice has been greatly facilitated by inducible and cell type-specific loss-of-function and gain-of-function genetics. In this paper, we provide a detailed protocol for tamoxifen-inducible gene deletion in neonatal mice, as well as for retina dissection, whole-mount immunostaining and the quantitation of EC sprouting and proliferation. These methods have been optimized by our laboratory and yield reliable results. The entire protocol takes approximately 10 d to complete.
视网膜是分析后生动物血管生成中血管生长的强大实验系统。血管网络的三维结构和多种过程,如内皮细胞(EC)增殖、发芽、血管周围细胞募集、血管重塑或成熟,可以高分辨率进行研究。通过诱导和细胞类型特异性的功能丧失和功能获得遗传学,极大地促进了对生理和病理血管生成过程的研究。在本文中,我们提供了一种详细的方案,用于诱导型和细胞类型特异性基因缺失在新生小鼠中的应用,以及用于视网膜解剖、全组织免疫染色和 EC 发芽和增殖的定量。这些方法已在我们的实验室中进行了优化,能够得到可靠的结果。整个方案大约需要 10 天完成。