| Literature DB >> 30594398 |
Eri Sone1, Daisuke Noshiro2, Yuki Ikebuchi3, Mami Nakagawa4, Masud Khan5, Yukihiko Tamura6, Masaomi Ikeda7, Meiko Oki5, Ramachandran Murali8, Toshihiko Fujimori4, Tetsuya Yoda9, Masashi Honma3, Hiroshi Suzuki3, Toshio Ando2, Kazuhiro Aoki10.
Abstract
We recently found that the membrane-bound receptor activator of NF-κB ligand (RANKL) on osteoblasts works as a receptor to stimulate osteoblast differentiation, however, the reason why the RANKL-binding molecules stimulate osteoblast differentiation has not been well clarified. Since the induction of cell-surface receptor clustering is known to lead to cell activation, we hypothesized that the induction of membrane-RANKL clustering on osteoblasts might stimulate osteoblast differentiation. Immunoblotting showed that the amount of RANKL on the membrane was increased by the RANKL-binding peptide OP3-4, but not by osteoprotegerin (OPG), the other RANKL-binding molecule, in Gfp-Rankl-transfected ST2 cells. Observation under a high-speed atomic force microscope (HS-AFM) revealed that RANKL molecules have the ability to form clusters. The induction of membrane-RANKL-OPG-Fc complex clustering by the addition of IgM in Gfp-Rankl-transfected ST2 cells could enhance the expression of early markers of osteoblast differentiation to the same extent as OP3-4, while OPG-Fc alone could not. These results suggest that the clustering-formation of membrane-RANKL on osteoblasts could stimulate early osteoblast differentiation.Entities:
Keywords: HS-AFM; OPG; Osteoblast differentiation; RANKL clustering; RANKL-binding peptide
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Year: 2018 PMID: 30594398 DOI: 10.1016/j.bbrc.2018.12.093
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575