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Riding Shotgun: A Dual Role for the Epidermal Growth Factor-Cripto/FRL-1/Cryptic Protein Cripto in Nodal Trafficking
被引:26
作者:
Constam, Daniel B.
[1
]
机构:
[1] EPFL, ISREC, CH-1066 Epalinges, Switzerland
来源:
关键词:
clathrin-independent endocytosis;
degradation;
flotillin;
multivesicular endosomes;
precursor processing;
proprotein convertases;
signal duration;
Smad anchor for receptor activation;
transforming growth factor beta;
GPI-ANCHORED PROTEINS;
FACTOR-BETA RECEPTOR;
EARLY MOUSE EMBRYO;
ONE-EYED-PINHEAD;
TGF-BETA;
INDEPENDENT ENDOCYTOSIS;
VERTEBRATE DEVELOPMENT;
MEMBRANE MICRODOMAINS;
MESODERM INDUCTION;
MORPHOGEN GRADIENT;
D O I:
10.1111/j.1600-0854.2009.00874.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071013 [干细胞生物学];
摘要:
Nodal is a secreted protein of the transforming growth factor beta (TGF beta) family that activates Smad2 and Smad3 transcription factors through complexes of type I and type II activin receptors and glycosyl-phosphatidylinositol-anchored coreceptors of the epidermal growth factor-like Cripto/FRL-1/Cryptic family. During early embryogenesis, it stimulates the proliferation of pluripotent progenitor cells and specifies, in a dosage-dependent manner, their subsequent allocation to distinct germ layers. Available evidence indicates that the signaling strength of Nodal is controlled at the level of endocytic uptake and turnover of activated receptor complexes in early endosomes, but insights into the underlying molecular mechanisms are still limited. In this review, I briefly survey literature on the trafficking of the related TGF beta receptors, and I discuss recent findings indicating that endocytosis of Nodal is coupled to proteolytic processing of its precursor at the cell surface and that the maturation and internalization of Nodal need to be guided by Cripto to stabilize endosomal signaling platforms.
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页码:783 / 791
页数:9
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