Eph Receptor Signaling and Ephrins

  1. Elena B. Pasquale1,3
  1. 1Cancer Center, Sanford-Burnham Medical Research Institute, La Jolla, California 92037
  2. 2Department of Pharmacology, University of Bologna, Bologna 40100, Italy
  3. 3Department of Pathology, University of California San Diego, La Jolla, California 92093
  1. Correspondence: elenap{at}sanfordburnham.org

Abstract

The Eph receptors are the largest of the RTK families. Like other RTKs, they transduce signals from the cell exterior to the interior through ligand-induced activation of their kinase domain. However, the Eph receptors also have distinctive features. Instead of binding soluble ligands, they generally mediate contact-dependent cell–cell communication by interacting with surface-associated ligands—the ephrins—on neighboring cells. Eph receptor–ephrin complexes emanate bidirectional signals that affect both receptor- and ephrin-expressing cells. Intriguingly, ephrins can also attenuate signaling by Eph receptors coexpressed in the same cell. Additionally, Eph receptors can modulate cell behavior independently of ephrin binding and kinase activity. The Eph/ephrin system regulates many developmental processes and adult tissue homeostasis. Its abnormal function has been implicated in various diseases, including cancer. Thus, Eph receptors represent promising therapeutic targets. However, more research is needed to better understand the many aspects of their complex biology that remain mysterious.



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