Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Traffic - International Journal of Intracellular Transport |
| Vol/bind | 10 |
| Udgave nummer | 8 |
| Sider (fra-til) | 1115-27 |
| Antal sider | 12 |
| ISSN | 1398-9219 |
| DOI | |
| Status | Udgivet - 2009 |
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I: Traffic - International Journal of Intracellular Transport, Bind 10, Nr. 8, 2009, s. 1115-27.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - Differential effects of EGFR ligands on endocytic sorting of the receptor
AU - Roepstorff, Kirstine
AU - Grandal, Michael Vibo
AU - Henriksen, Lasse
AU - Knudsen, Stine Louise Jeppe
AU - Lerdrup, Mads
AU - Grøvdal, Lene
AU - Willumsen, Berthe Marie
AU - van Deurs, Bo
PY - 2009
Y1 - 2009
N2 - Endocytic downregulation is a pivotal mechanism turning off signalling from the EGF receptor (EGFR). It is well established that whereas EGF binding leads to lysosomal degradation of EGFR, transforming growth factor (TGF)-alpha causes receptor recycling. TGF-alpha therefore leads to continuous signalling and is a more potent mitogen than EGF. In addition to EGF and TGF-alpha, five EGFR ligands have been identified. Although many of these ligands are upregulated in cancers, very little is known about their effect on EGFR trafficking. We have compared the effect of six different ligands on endocytic trafficking of EGFR. We find that, whereas they all stimulate receptor internalization, they have very diverse effects on endocytic sorting. Heparin-binding EGF-like growth factor and Betacellulin target all EGFRs for lysosomal degradation. In contrast, TGF-alpha and epiregulin lead to complete receptor recycling. EGF leads to lysosomal degradation of the majority but not all EGFRs. Amphiregulin does not target EGFR for lysosomal degradation but causes fast as well as slow EGFR recycling. The Cbl ubiquitin ligases, especially c-Cbl, are responsible for EGFR ubiquitination after stimulation with all ligands, and persistent EGFR phosphorylation and ubiquitination largely correlate with receptor degradation.
AB - Endocytic downregulation is a pivotal mechanism turning off signalling from the EGF receptor (EGFR). It is well established that whereas EGF binding leads to lysosomal degradation of EGFR, transforming growth factor (TGF)-alpha causes receptor recycling. TGF-alpha therefore leads to continuous signalling and is a more potent mitogen than EGF. In addition to EGF and TGF-alpha, five EGFR ligands have been identified. Although many of these ligands are upregulated in cancers, very little is known about their effect on EGFR trafficking. We have compared the effect of six different ligands on endocytic trafficking of EGFR. We find that, whereas they all stimulate receptor internalization, they have very diverse effects on endocytic sorting. Heparin-binding EGF-like growth factor and Betacellulin target all EGFRs for lysosomal degradation. In contrast, TGF-alpha and epiregulin lead to complete receptor recycling. EGF leads to lysosomal degradation of the majority but not all EGFRs. Amphiregulin does not target EGFR for lysosomal degradation but causes fast as well as slow EGFR recycling. The Cbl ubiquitin ligases, especially c-Cbl, are responsible for EGFR ubiquitination after stimulation with all ligands, and persistent EGFR phosphorylation and ubiquitination largely correlate with receptor degradation.
U2 - 10.1111/j.1600-0854.2009.00943.x
DO - 10.1111/j.1600-0854.2009.00943.x
M3 - Journal article
C2 - 19531065
SN - 1398-9219
VL - 10
SP - 1115
EP - 1127
JO - Traffic - International Journal of Intracellular Transport
JF - Traffic - International Journal of Intracellular Transport
IS - 8
ER -