Irreversible inhibition of RANK expression as a possible mechanism for IL-3 inhibition of RANKL-induced osteoclastogenesis

被引:10
|
作者
Khapli, Shruti M. [1 ]
Tomar, Geetanjali B. [1 ]
Barhanpurkar, Amruta P. [1 ]
Gupta, Navita [1 ]
Yogesha, S. D. [1 ]
Pote, Satish T. [1 ]
Wani, Mohan R. [1 ]
机构
[1] Natl Ctr Cell Sci, Pune 411007, Maharashtra, India
关键词
IL-3; Osteoclast differentiation; RANKL; Transcription factors; RANK signaling pathways; COLONY-STIMULATING FACTOR; N-TERMINAL KINASE; C-JUN; RECEPTOR ACTIVATOR; KEY REGULATOR; T-CELLS; KAPPA-B; OSTEOPROTEGERIN LIGAND; MACROPHAGE LINEAGE; NUCLEAR-FACTOR;
D O I
10.1016/j.bbrc.2010.07.143
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IL-3, a cytokine secreted by activated T lymphocytes, stimulates the proliferation, differentiation and survival of pluripotent hematopoietic stem cells. In this study, we investigated the mechanism of inhibitory action of IL-3 on osteoclast differentiation. We show here that IL-3 significantly inhibits receptor activator of NF-kappa B (RANK) ligand (RANKL)-induced activation of c-Jun N-terminal kinase (JNK). IL-3 down-regulates expression of c-Fos and nuclear factor of activated T cells (NFATc1) transcription factors. In addition, IL-3 down-regulates RANK expression posttranscriptionally in both purified osteoclast precursors and whole bone marrow cells. Furthermore, the inhibitory effect of IL-3 on RANK expression was irreversible. Interestingly, IL-3 inhibits in vivo RANK expression in mice. Thus, we provide the first evidence that IL-3 irreversibly inhibits RANK expression that results in inhibition of important signaling molecules induced by RANKL (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:688 / 693
页数:6
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