TY - JOUR
T1 - Receptor activator of nuclear factor-κB ligand activates nuclear factor-κB in osteoclast precursors
AU - Wei, Shi
AU - Teitelbaum, Steven L.
AU - Wang, Michael W.H.
AU - Ross, F. Patrick
PY - 2001
Y1 - 2001
N2 - Receptor activator of nuclear factor-κB ligand [RANK ligand (RANK-L)] stimulates mature osteoclasts to resorb bone, a process associated with NF-κB activation. RANK-L also prompts macrophages to develop the osteoclast phenotype. Although NF-κB is essential for osteoclast differentiation, it is not known whether RANK-L activates this transcription complex in osteoclast precursors. We report that RANK-L rapidly induces NF-κB activation in both authentic osteoclast precursors, namely bone marrow macrophages, and RAW 264.7 cells, a murine macrophage line also capable of RANK-L-mediated osteoclastogenesis. Supershift studies reveal the RANK-L-induced DNA binding moiety contains p50/p65, the most common NF-κB complex. Subcellular translocation of p50 and p65 subunits is confirmed by Western blots and immunofluorescence analysis. RANK-L activates NF-κB in both bone marrow macrophages and RAW 264.7 cells by serine phosphorylation of IκBα within 5 min, resulting in rapid IκBα degradation and resynthesis. Attesting to function, RANK-L treatment of RAW 264.7 cells transiently transfected with a plasmid containing NF-κB consensus elements linked to luciferase greatly enhances reporter activity. Our data suggest that activation of the NF-κB pathway is an integral component of RANK-L-induced osteoclast differentiation.
AB - Receptor activator of nuclear factor-κB ligand [RANK ligand (RANK-L)] stimulates mature osteoclasts to resorb bone, a process associated with NF-κB activation. RANK-L also prompts macrophages to develop the osteoclast phenotype. Although NF-κB is essential for osteoclast differentiation, it is not known whether RANK-L activates this transcription complex in osteoclast precursors. We report that RANK-L rapidly induces NF-κB activation in both authentic osteoclast precursors, namely bone marrow macrophages, and RAW 264.7 cells, a murine macrophage line also capable of RANK-L-mediated osteoclastogenesis. Supershift studies reveal the RANK-L-induced DNA binding moiety contains p50/p65, the most common NF-κB complex. Subcellular translocation of p50 and p65 subunits is confirmed by Western blots and immunofluorescence analysis. RANK-L activates NF-κB in both bone marrow macrophages and RAW 264.7 cells by serine phosphorylation of IκBα within 5 min, resulting in rapid IκBα degradation and resynthesis. Attesting to function, RANK-L treatment of RAW 264.7 cells transiently transfected with a plasmid containing NF-κB consensus elements linked to luciferase greatly enhances reporter activity. Our data suggest that activation of the NF-κB pathway is an integral component of RANK-L-induced osteoclast differentiation.
UR - http://www.scopus.com/inward/record.url?scp=0035092848&partnerID=8YFLogxK
U2 - 10.1210/endo.142.3.8031
DO - 10.1210/endo.142.3.8031
M3 - Article
C2 - 11181547
AN - SCOPUS:0035092848
VL - 142
SP - 1290
EP - 1295
JO - Endocrinology
JF - Endocrinology
SN - 0013-7227
IS - 3
ER -