HRS regulates endosomal trafficking and tyrosine kinase receptor signaling

2001 ◽  
Vol 29 (3) ◽  
pp. A84-A84
Author(s):  
T. E. Lloyd ◽  
R. A. Atkinson ◽  
M. N. Wu ◽  
H. J. Bellen
2008 ◽  
Vol 182 (5) ◽  
pp. 823-825 ◽  
Author(s):  
Marisa P. McShane ◽  
Marino Zerial

The tyrosine kinase receptor c-Met plays a key role in cell proliferation, morphogenesis, and motility in response to hepatocyte growth factor. C-Met is often altered in cancer and is a major target for therapeutic intervention. Despite knowing a great deal of the molecular machinery downstream of this receptor tyrosine kinase, the spatiotemporal regulation of c-Met signaling still remains elusive. In this issue of the Journal of Cell Biology, Kermorgant and Parker (Kermorgant, S. and P.J. Parker. 2008. J. Cell Biol. 182:855–863) provide evidence for a model in which the c-Met–activated STAT3 signal is mediated by endosomal trafficking. This study elegantly highlights how weak signals can be effectively transmitted to the nucleus by exploiting endosomal compartments, raising important mechanistic implications for the signaling research community.


Cell ◽  
2002 ◽  
Vol 108 (2) ◽  
pp. 261-269 ◽  
Author(s):  
Thomas E. Lloyd ◽  
Richard Atkinson ◽  
Mark N. Wu ◽  
Yi Zhou ◽  
Giuseppa Pennetta ◽  
...  

2014 ◽  
Author(s):  
Marlen Zschätzsch ◽  
Carlos Oliva ◽  
Marion Langen ◽  
Natalie De Geest ◽  
Mehmet Neset Özel ◽  
...  

2011 ◽  
pp. P2-276-P2-276
Author(s):  
Smita Salian Mehta ◽  
Mei Xu ◽  
Melinda Schaller ◽  
Margaret E Wierman

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