Cripto recruits Furin and PACE4 and controls Nodal trafficking during proteolytic maturation

被引:62
作者
Blanchet, Marie-Helene [1 ]
Le Good, J. Ann [1 ]
Mesnard, Daniel [1 ]
Oorschot, Viola [2 ]
Baflast, Stephane [1 ]
Minchiotti, Gabriella [3 ]
Klumperman, Judith [2 ]
Constam, Daniel B. [1 ]
机构
[1] Swiss Inst Expt Canc Res ISREC, EPFL, CH-1066 Epalinges, Switzerland
[2] Cell Microscopy Ctr, Dept Cell Biol, Utrecht, Netherlands
[3] Inst Genet & Biophys A Buzzati Traverso, Naples, Italy
基金
瑞士国家科学基金会;
关键词
EGF-CFC; TGF beta; trafficking; unconventional exocytosis;
D O I
10.1038/emboj.2008.174
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The glycosylphosphatidylinositol (GPI)-anchored proteoglycan Cripto binds Nodal and its type I receptor Alk4 to activate Smad2,3 transcription factors, but a role during Nodal precursor processing has not been described. We show that Cripto also binds the proprotein convertases Furin and PACE4 and localizes Nodal processing at the cell surface. When coexpressed as in early embryonic cells, Cripto and uncleaved Nodal already associated during secretion, and a Cripto-interacting region in the Nodal propeptide potentiated the effect of proteolytic maturation on Nodal signalling. Disruption of the trans-Golgi network (TGN) by brefeldin A blocked secretion, but export of Cripto and Nodal to the cell surface was not inhibited, indicating that Nodal is exposed to extracellular convertases before entering the TGN/endosomal system. Density fractionation and antibody uptake experiments showed that Cripto guides the Nodal precursor in detergent-resistant membranes to endocytic microdomains marked by GFP-Flotillin. We conclude that Nodal processing and endocytosis are coupled in signal-receiving cells.
引用
收藏
页码:2580 / 2591
页数:12
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