Document Detail


Osteoclastogenesis and osteoclastic resorption of tricalcium phosphate: effect of strontium and magnesium doping.
MedLine Citation:
PMID:  22566212     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Bone substitute materials are required to support the remodeling process, which consists of osteoclastic resorption and osteoblastic synthesis. Osteoclasts, the bone-resorbing cells, generate from differentiation of hemopoietic mononuclear cells. In the present study, we have evaluated the effects of 1.0 wt % strontium (Sr) and 1.0 wt % magnesium (Mg) doping in beta-tricalcium phosphate (β-TCP) on the differentiation of mononuclear cells into osteoclast-like cells and its resorptive activity. In vitro osteoclast-like cell formation, adhesion, and resorption were studied using osteoclast precursor RAW 264.7 cell, supplemented with receptor activator of nuclear factor κβ ligand (RANKL). Osteoclast-like cell formation was noticed on pure and Sr-doped β-TCP samples at day 8, which was absent on Mg-doped β-TCP samples indicating decrease in initial osteoclast differentiation due to Mg doping. After 21 days of culture, osteoclast-like cell formation was evident on all samples with osteoclastic markers such as actin ring, multiple nuclei, and presence of vitronectin receptor α(v)β(3) integrin. After osteoclast differentiation, all substrates showed osteoclast-like cell-mediated degradation, however, significantly restricted for Mg-doped β-TCP samples. Our present results indicated that substrate chemistry controlled osteoclast differentiation and resorptive activity, which can be used in designing TCP-based resorbable bone substitutes with controlled degradation properties.
Authors:
Mangal Roy; Susmita Bose
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2012-05-05
Journal Detail:
Title:  Journal of biomedical materials research. Part A     Volume:  100     ISSN:  1552-4965     ISO Abbreviation:  J Biomed Mater Res A     Publication Date:  2012 Sep 
Date Detail:
Created Date:  2012-07-25     Completed Date:  2012-11-27     Revised Date:  2013-04-16    
Medline Journal Info:
Nlm Unique ID:  101234237     Medline TA:  J Biomed Mater Res A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  2450-61     Citation Subset:  IM    
Copyright Information:
Copyright © 2012 Wiley Periodicals, Inc.
Affiliation:
W M Keck Biomedical Materials Research Laboratory, School of Mechanical and Materials Engineering, Washington State University, Pullman, Washington 99164, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Bone Substitutes / chemistry,  metabolism*
Calcium Phosphates / chemistry,  metabolism*
Cell Adhesion
Cell Differentiation
Cell Line
Magnesium / chemistry,  metabolism*
Mice
Osteoclasts / cytology*,  metabolism
RANK Ligand / metabolism
Strontium / chemistry,  metabolism*
Grant Support
ID/Acronym/Agency:
N1H-R01-EB-007351/EB/NIBIB NIH HHS; R01 EB007351/EB/NIBIB NIH HHS
Chemical
Reg. No./Substance:
0/Bone Substitutes; 0/Calcium Phosphates; 0/RANK Ligand; 0/beta-tricalcium phosphate; 7439-95-4/Magnesium; 7440-24-6/Strontium

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  A General Approach to Optically Pure [5]-, [6]-, and [7]Heterohelicenes.
Next Document:  Rhodium(II)- and Copper(II)-Catalyzed Reactions of Enol Diazoacetates with Nitrones: Metal Carbene v...