Vascular-mesenchymal cross-talk through Vegf and Pdgf drives organ patterning

被引:83
作者
Cool, Jonah [1 ]
DeFalco, Tony J. [1 ]
Capel, Blanche [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
organogenesis; sex determination; testis formation; CELL-PROLIFERATION; XY GONAD; CORD FORMATION; GROWTH-FACTOR; STEM-CELLS; TESTIS; NICHE; MICE; DIFFERENTIATION; MORPHOGENESIS;
D O I
10.1073/pnas.1010299108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The initiation of de novo testis cord organization in the fetal gonad is poorly understood. Endothelial cell migration into XY gonads initiates testis morphogenesis. However, neither the signals that regulate vascularization of the gonad nor the mechanisms through which vessels affect tissue morphogenesis are known. Here, we show that Vegf signaling is required for gonad vascularization and cord morphogenesis. We establish that interstitial cells express Vegfa and respond, by proliferation, to endothelial migration. In the absence of vasculature, four-dimensional imaging of whole organs revealed that interstitial proliferation is reduced and prevents formation of wedge-like structures that partition the gonad into cord-forming domains. Antagonizing vessel maturation also reduced proliferation. However, proliferation of mesenchymal cells was rescued by the addition of PDGF-BB. These results suggest a pathway that integrates initiation of vascular development and testis cord morphogenesis, and lead to a model in which undifferentiated mesenchyme recruits blood vessels, proliferates in response, and performs a primary function in the morphogenesis and patterning of the developing organ.
引用
收藏
页码:167 / 172
页数:6
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