Fgf8 morphogen gradient forms by a source-sink mechanism with freely diffusing molecules

被引:289
作者
Yu, Shuizi Rachel [1 ,2 ]
Burkhardt, Markus [1 ,2 ]
Nowak, Matthias [1 ,2 ]
Ries, Jonas [1 ,2 ]
Petrasek, Zdenek [1 ,2 ]
Scholpp, Steffen [1 ]
Schwille, Petra [1 ,2 ]
Brand, Michael [1 ,2 ]
机构
[1] TUD, Ctr Biotechnol, D-01307 Dresden, Germany
[2] TUD, Ctr Regenerat Therapies, D-01307 Dresden, Germany
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; EARLY XENOPUS EMBRYO; CROSS-CORRELATION; ZEBRAFISH; DIFFERENTIATION; ENDOCYTOSIS; TRANSPORT; DYNAMICS; PATTERN; RANGE;
D O I
10.1038/nature08391
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
07 ; 0710 ; 09 ;
摘要
It is widely accepted that tissue differentiation and morphogenesis in multicellular organisms are regulated by tightly controlled concentration gradients of morphogens(1,2). How exactly these gradients are formed, however, remains unclear(3-12). Here we show that Fgf8 morphogen gradients in living zebrafish embryos are established andmaintained by two essential factors: fast, free diffusion of single molecules away from the source through extracellular space, and a sink function of the receiving cells, regulated by receptor-mediated endocytosis. Evidence is provided by directly examining single molecules of Fgf8 in living tissue by fluorescence correlation spectroscopy, quantifying their local mobility and concentration with high precision. By changing the degree of uptake of Fgf8 into its target cells, we are able to alter the shape of the Fgf8 gradient. Our results demonstrate that a freely diffusing morphogen can set up concentration gradients in a complex multicellular tissue by a simple source-sink mechanism.
引用
收藏
页码:533 / U100
页数:5
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