Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells

Lipopolysaccharide (LPS) is bacterial cell wall component capable of inducing osteoclast formation and pathological bone resorption. Muramyl dipeptide (MDP), the minimal essential structural unit responsible for the immunological activity of peptidoglycans, is ubiquitously expressed by bacterium. In...

Full description

Saved in:
Bibliographic Details
Main Authors: Masahiko Ishida, Hideki Kitaura, Keisuke Kimura, Haruki Sugisawa, Tomo Aonuma, Haruhiko Takada, Teruko Takano-Yamamoto
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2015/132765
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832563272685977600
author Masahiko Ishida
Hideki Kitaura
Keisuke Kimura
Haruki Sugisawa
Tomo Aonuma
Haruhiko Takada
Teruko Takano-Yamamoto
author_facet Masahiko Ishida
Hideki Kitaura
Keisuke Kimura
Haruki Sugisawa
Tomo Aonuma
Haruhiko Takada
Teruko Takano-Yamamoto
author_sort Masahiko Ishida
collection DOAJ
description Lipopolysaccharide (LPS) is bacterial cell wall component capable of inducing osteoclast formation and pathological bone resorption. Muramyl dipeptide (MDP), the minimal essential structural unit responsible for the immunological activity of peptidoglycans, is ubiquitously expressed by bacterium. In this study, we investigated the effect of MDP in LPS-induced osteoclast formation and bone resorption. LPS was administered with or without MDP into the supracalvariae of mice. The number of osteoclasts, the level of mRNA for cathepsin K and tartrate-resistant acid phosphatase (TRAP), the ratio of the bone destruction area, the level of tartrate-resistant acid phosphatase form 5b (TRACP 5b), and C-terminal telopeptides fragments of type I collagen as a marker of bone resorption in mice administrated both LPS and MDP were higher than those in mice administrated LPS or MDP alone. On the other hand, MDP had no effect on osteoclastogenesis in parathyroid hormone administrated mice. MDP enhanced LPS-induced receptor activator of NF-κB ligand (RANKL) expression and Toll-like receptor 4 (TLR4) expression in vivo and in stromal cells in vitro. MDP also enhanced LPS-induced mitogen-activated protein kinase (MAPK) signaling, including ERK, p38, and JNK, in stromal cells. These results suggest that MDP might play an important role in pathological bone resorption in bacterial infection diseases.
format Article
id doaj-art-212e6de8d2b94ee49fabf0464b631164
institution Kabale University
issn 2314-8861
2314-7156
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Journal of Immunology Research
spelling doaj-art-212e6de8d2b94ee49fabf0464b6311642025-02-03T01:20:29ZengWileyJournal of Immunology Research2314-88612314-71562015-01-01201510.1155/2015/132765132765Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal CellsMasahiko Ishida0Hideki Kitaura1Keisuke Kimura2Haruki Sugisawa3Tomo Aonuma4Haruhiko Takada5Teruko Takano-Yamamoto6Division of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDivision of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDivision of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDivision of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDivision of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDepartment of Microbiology and Immunology, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanDivision of Orthodontics and Dentofacial Orthopedics, Department of Translational Medicine, Tohoku University Graduate School of Dentistry, 4-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, JapanLipopolysaccharide (LPS) is bacterial cell wall component capable of inducing osteoclast formation and pathological bone resorption. Muramyl dipeptide (MDP), the minimal essential structural unit responsible for the immunological activity of peptidoglycans, is ubiquitously expressed by bacterium. In this study, we investigated the effect of MDP in LPS-induced osteoclast formation and bone resorption. LPS was administered with or without MDP into the supracalvariae of mice. The number of osteoclasts, the level of mRNA for cathepsin K and tartrate-resistant acid phosphatase (TRAP), the ratio of the bone destruction area, the level of tartrate-resistant acid phosphatase form 5b (TRACP 5b), and C-terminal telopeptides fragments of type I collagen as a marker of bone resorption in mice administrated both LPS and MDP were higher than those in mice administrated LPS or MDP alone. On the other hand, MDP had no effect on osteoclastogenesis in parathyroid hormone administrated mice. MDP enhanced LPS-induced receptor activator of NF-κB ligand (RANKL) expression and Toll-like receptor 4 (TLR4) expression in vivo and in stromal cells in vitro. MDP also enhanced LPS-induced mitogen-activated protein kinase (MAPK) signaling, including ERK, p38, and JNK, in stromal cells. These results suggest that MDP might play an important role in pathological bone resorption in bacterial infection diseases.http://dx.doi.org/10.1155/2015/132765
spellingShingle Masahiko Ishida
Hideki Kitaura
Keisuke Kimura
Haruki Sugisawa
Tomo Aonuma
Haruhiko Takada
Teruko Takano-Yamamoto
Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
Journal of Immunology Research
title Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
title_full Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
title_fullStr Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
title_full_unstemmed Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
title_short Muramyl Dipeptide Enhances Lipopolysaccharide-Induced Osteoclast Formation and Bone Resorption through Increased RANKL Expression in Stromal Cells
title_sort muramyl dipeptide enhances lipopolysaccharide induced osteoclast formation and bone resorption through increased rankl expression in stromal cells
url http://dx.doi.org/10.1155/2015/132765
work_keys_str_mv AT masahikoishida muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT hidekikitaura muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT keisukekimura muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT harukisugisawa muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT tomoaonuma muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT haruhikotakada muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells
AT terukotakanoyamamoto muramyldipeptideenhanceslipopolysaccharideinducedosteoclastformationandboneresorptionthroughincreasedranklexpressioninstromalcells