Inducible gene targeting in the neonatal vasculature and analysis of retinal angiogenesis in mice

被引:319
作者
Pitulescu, Mara E. [1 ]
Schmidt, Inga [1 ]
Benedito, Rui [1 ]
Adams, Ralf H. [1 ]
机构
[1] Univ Munster, Dept Tissue Morphogenesis, Fac Med, Max Planck Inst Mol Biomed, Munster, Germany
关键词
3-DIMENSIONAL COLLAGEN; ENDOTHELIAL-CELLS; BASEMENT-MEMBRANE; IN-VITRO; CRE-RECOMBINASE; LUMEN FORMATION; MODELS; MOUSE; DIFFERENTIATION; EPHRIN-B2;
D O I
10.1038/nprot.2010.113
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 similar to 10 d to complete.
引用
收藏
页码:1518 / 1534
页数:17
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