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Publication : Inhibition effect of enteropeptidase on RANKL-RANK signalling by cleavage of RANK.

First Author  Zhao Y Year  2013
Journal  FEBS Lett Volume  587
Issue  18 Pages  2958-64
PubMed ID  23954298 Mgi Jnum  J:200980
Mgi Id  MGI:5510605 Doi  10.1016/j.febslet.2013.08.005
Citation  Zhao Y, et al. (2013) Inhibition effect of enteropeptidase on RANKL-RANK signalling by cleavage of RANK. FEBS Lett 587(18):2958-64
abstractText  Enteropeptidase can cleave trypsinogen on the sequence of Asp-Asp-Asp-Asp-Lys and plays an important role in food digestion. The RANKL-RANK signalling pathway plays a pivotal role in bone remodelling. In this study, we reported that enteropeptidase can inhibit the RANKL-RANK signalling pathway through the cleavage of RANK. A surrogate peptide blocking assay indicated that enteropeptidase could specifically cleave RANK on the sequence NEEDK. Osteoclast differentiation assay and NF-kappaB activity assay confirmed that enteropeptidase could inhibit osteoclastogenesis in vitro through the cleavage of RANK. This is the first study to prove that the RANKL-RANK signalling pathway can be inhibited by cleavage of RANK instead of targeting RANKL. STRUCTURED SUMMARY OF PROTEIN INTERACTIONS: EPcleaveshRANK by cleavage assay (View interaction) EPcleavesmRANK by cleavage assay (View interaction).
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