{Reference Type}: Journal Article
{Title}: S100P binds to RAGE and activates ERK/NF-κB signaling to promote osteoclast differentiation and activity.
{Author}: Lee SH;Park NR;Park EK;Kim JE;
{Journal}: Biochem Biophys Res Commun
{Volume}: 738
{Issue}: 0
{Year}: 2024 Aug 12
{Factor}: 3.322
{DOI}: 10.1016/j.bbrc.2024.150536
{Abstract}: S100 calcium-binding protein P (S100P) is a secretory protein that is expressed in various healthy tissues and tumors. Megakaryocyte-secreted S100P promotes osteoclast differentiation and function; however, its receptor and cellular signaling in osteoclasts remain unclear. Receptor for advanced glycation end products (RAGE), which is the receptor for S100P on cancer cells, was expressed in osteoclast precursors, and S100P-RAGE binding was confirmed through co-immunoprecipitation. Additionally, the phosphorylation of ERK and NF-κB was increased in S100P-stimulated osteoclast precursors but was inhibited by addition of the RAGE antagonistic peptide (RAP). S100P-induced osteoclast differentiation and excessive bone resorption activity were also reduced by the addition of RAP. This study demonstrates that S100P, upon binding with RAGE, activates the ERK and NF-κB signaling pathways in osteoclasts, leading to increased cell differentiation and bone resorption activity.