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J Biol Chem. 2017 Sep 15;292(37):15192-15204. doi: 10.1074/jbc.M117.783845. Epub 2017 Jun 30.

Neuropilin-1 promotes Hedgehog signaling through a novel cytoplasmic motif.

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From the Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109.
From the Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109


Hedgehog (HH) signaling critically regulates embryonic and postnatal development as well as adult tissue homeostasis, and its perturbation can lead to developmental disorders, birth defects, and cancers. Neuropilins (NRPs), which have well-defined roles in Semaphorin and VEGF signaling, positively regulate HH pathway function, although their mechanism of action in HH signaling remains unclear. Here, using luciferase-based reporter assays, we provide evidence that NRP1 regulates HH signaling specifically at the level of GLI transcriptional activator function. Moreover, we show that NRP1 localization to the primary cilium, a key platform for HH signal transduction, does not correlate with HH signal promotion. Rather, a structure-function analysis suggests that the NRP1 cytoplasmic and transmembrane domains are necessary and sufficient to regulate HH pathway activity. Furthermore, we identify a previously uncharacterized, 12-amino acid region within the NRP1 cytoplasmic domain that mediates HH signal promotion. Overall, our results provide mechanistic insight into NRP1 function within and potentially beyond the HH signaling pathway. These insights have implications for the development of novel modulators of HH-driven developmental disorders and diseases.


Hedgehog signaling pathway; Neuropilin; PKA; cell signaling; cell surface receptor; cilia; signal transduction

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