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Impediment of NEMO oligomerization inhibits osteoclastogenesis and osteolysis
Author(s) -
Darwech Isra,
Otero Jesse,
Alhawagri Muhammad,
Dai Simon,
AbuAmer Yousef
Publication year - 2009
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.22364
Subject(s) - osteolysis , rankl , osteoclast , chemistry , nf κb , iκb kinase , microbiology and biotechnology , cancer research , iκbα , signal transduction , rank ligand , transcription factor , in vitro , biochemistry , activator (genetics) , receptor , medicine , biology , surgery , gene
Abstract The transcription factor NF‐κB is essential for osteoclastogenesis and is considered an immune‐modulator of rheumatoid arthritis and inflammatory osteolysis. Activation of NF‐κB subunits is regulated by the upstream IκB kinase (IKK) complex which contains IKKα, IKKβ, and IKKγ; the latter also known as NF‐κB essential modulator (NEMO). The role of IKKα and IKKβ in the skeletal development and inflammatory osteolysis has been described, whereas little is known regarding the role of NEMO in this setting. Typically, signals induced by RANK ligand (RANKL) or TNF prompt oligomerization of NEMO monomers through the coiled‐coil‐2 (CC2) and leucine zipper (LZ) motifs. This step facilitates binding to IKKs and further relaying signal transduction. Given the central role of NF‐κB in osteoclastogenesis, we asked whether NEMO is essential for osteoclastogenesis and whether interruption of NEMO oligomerization impedes osteoclast differentiation in vitro and in vivo. Using cell‐permeable short peptides overlapping the CC2 and LZ motifs we show that these peptides specifically bind to NEMO monomers, prevent trimer formation, and render NEMO monomers susceptible for ubiquitin‐mediated degradation. Further, CC2 and LZ peptides attenuate RANKL‐ and TNF‐induced NF‐κB signaling in bone marrow‐derived osteoclast precursors (OCPs). More importantly, these peptides potently inhibit osteoclastogenesis, in vitro, and arrest RANKL‐induced osteolysis, in mice. To further ascertain its role in osteoclastogenesis, we were able to block osteoclastogenesis using NEMO siRNA knockdown approach. Collectively, our data establish that obstruction of NEMO oligomerization destabilizes NEMO monomers, inhibits NF‐κB activation, impedes osteoclastogenesis and arrests inflammatory osteolysis. Thus, NEMO presents itself as a promising target for anti‐osteolytic intervention. J. Cell. Biochem. 108: 1337–1345, 2009. © 2009 Wiley‐Liss, Inc.