Evidence That Receptor Activator of Nuclear Factor (NF)-[kappa]B Ligand Can Suppress Cell Proliferation and Induce Apoptosis through Activation of a NF- [kappa]B-independent and TRAF6-dependent Mechanism

• Published in: The Journal of biological chemistry 2004-02, Vol.279 (7), p.6065-6076
• Main Authors: Bharti, A C, Takada, Y, Shishodia, S, Aggarwal, B B
• Format: Article
• Language: English
• Subjects: cyclin D1; cyclin D3; cyclin E; NF-B protein; RANKL protein; RAW 264.7 cells; TRAF6 protein
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M308062200

The receptor activator of NF-[kappa]B ligand (RANKL), a recently identified member of the tumor necrosis factor (TNF) superfamily, has been shown to induce osteoclastogenesis and dendritic cell survival. Most members of the TNF superfamily suppress cell proliferation and induce apoptosis, but whether RANKL does so is not known. We demonstrate that treatment of monocyte RAW 264.7 cells with RANKL induces dose-dependent growth inhibition (IC sub(50) = 10 ng/ml) as determined by dye uptake and [ super(3)H]thymidine incorporation methods. Suppression of RANKL-induced NF-[kappa]B activation by dominant-negative I[kappa]B[alpha] or by the NEMO-peptide had no effect on RANKL-induced cell growth inhibition. Inhibition of RANKL-induced JNK activation, however, abolished the RANKL-induced apoptosis. Suppression of interaction of RANK with TRAF6 by TRAF6-binding peptide abrogated the anti-proliferative effects of RANKL, suggesting the critical role of TRAF6. Flow cytometric analysis of cells treated with RANKL showed accumulation of cells in G sub(0)/G sub(1) phase of the cell cycle, and this accumulation correlated with a decline in the levels of cyclin D1, cyclin D3, and cyclin E and an increase in cyclin-dependent kinase inhibitor p27 (Kip). Flow cytometric analysis showed the presence of annexin V- positive cells in cultures treated with RANKL. RANKL-induced apoptosis was further confirmed using calcein AM/ethidium homodimer-1 dye and cleavage of poly(ADP-ribose) polymerase (PARP), procaspase 3, and procaspase 9; benzyloxycarbonyl-VAD, the pancaspase inhibitor, suppressed the PARP cleavage. Thus, overall, our studies indicate that RANKL can inhibit cell proliferation and induce apoptosis through a TRAF-6-dependent but NF-[kappa]B-independent mechanism.