Effect of Anti-c-fms Antibody on Osteoclast Formation and Proliferation of Osteoclast Precursor In Vitro.
Animals
Antibodies
/ pharmacology
Cell Differentiation
/ physiology
Cell Proliferation
/ drug effects
Macrophage Colony-Stimulating Factor
/ pharmacology
Mice, Inbred C57BL
Osteoclasts
/ cytology
RANK Ligand
/ pharmacology
Receptor, Macrophage Colony-Stimulating Factor
/ immunology
Tumor Necrosis Factor-alpha
/ pharmacology
Journal
Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252
Informations de publication
Date de publication:
18 03 2019
18 03 2019
Historique:
entrez:
2
4
2019
pubmed:
2
4
2019
medline:
31
1
2020
Statut:
epublish
Résumé
Bone remodeling is a complex process and it involves periods of deposition and resorption. Bone resorption is a process by which bone is broken down by osteoclasts in response to different stimuli. Osteoclast precursors differentiate into multinuclear osteoclasts in response to macrophage colony stimulating factor (M-CSF) and receptor activator of nuclear factor Kappa-B ligand (RANKL). Under pathologic conditions, the cytokine profile is different and involves a mixture of inflammatory cytokines. Tumor necrosis factor alpha (TNF-α) is one of the most important cytokines as it is found in large amounts in areas involved with inflammatory osteolysis. The purpose of this protocol is to provide a method by which murine bone marrow is isolated to generate osteoclasts through induction with M-CSF and either RANKL or TNF-α which will be subsequently inhibited by increasing doses of anti-c-fms antibody, the receptor for M-CSF. This experiment highlights the therapeutic value of anti-c-fms antibody in diseases of inflammatory bone resorption.
Substances chimiques
Antibodies
0
RANK Ligand
0
Tumor Necrosis Factor-alpha
0
Macrophage Colony-Stimulating Factor
81627-83-0
Receptor, Macrophage Colony-Stimulating Factor
EC 2.7.10.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Video-Audio Media
Langues
eng
Sous-ensembles de citation
IM