Journal of Biological Chemistry · 2013 · 73 citations · 49 references
Life SciencesDevelopmental BiologyNeuroscienceCell SignalingDevelopmental NeuroscienceSignal TransductionExtracellular Matrix GlycansGlycan StructureGlycan-protein InteractionsGrowth Factor SignalingHedgehog SignalingAxonal GuidanceHedgehog Signaling In ProliferationHeparan Sulfate ProteoglycansHeparan Sulfate SignalingNeural ProliferationPatched Receptor SignalingReceptorsSignaling
Sonic Hedgehog (Shh) signaling is crucial for growth, cell fate determination, and axonal guidance in the developing nervous system. Although the receptors Patched (Ptch1) and Smoothened (Smo) are required for Shh signaling, a number of distinct co-receptors contribute to these critical responses to Shh. Several membrane-embedded proteins such as Boc, Cdo, and Gas1 bind Shh and promote signaling. In addition, heparan sulfate proteoglycans (HSPGs) have also been implicated in the initiation of Shh responses. However, the attributes of HSPGs that function as co-receptors for Shh have not yet been defined. Here, we identify HSPGs containing a glypican 5 core protein and 2-O-sulfo-iduronic acid residues at the nonreducing ends of the glycans as co-receptors for Shh. These HSPG co-receptors are expressed by cerebellar granule cell precursors and promote Shh binding and signaling. At the subcellular level, these HSPG co-receptors are located adjacent to the primary cilia that act as Shh signaling organelles. Thus, Shh binds to HSPG co-receptors containing a glypican 5 core and 2-O-sulfo-iduronic acid to promote neural precursor proliferation. Background: The nature of proteoglycans that function as co-receptors for Sonic Hedgehog (Shh) is not known. Results: Glypican 5 and 2-O-sulfo-iduronic acid are expressed in neural precursors, adjacent to primary cilia. Elimination of these components reduce Shh signaling. Conclusion: Glypican 5 bearing 2-O-sulfo-iduronic acid at the nonreducing ends is a Shh co-receptor. Significance: Attributes of Shh co-receptors have been identified.
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