Document Detail

Effects of polyelectrolytic peptides on the quality of mineral crystals grown in vitro.
MedLine Citation:
PMID:  18979156     Owner:  NLM     Status:  MEDLINE    
Charged amino acids such as arginine, lysine, glutamic acid, and aspartic acid are abundant in noncollagenous proteins that regulate mineralization. Synthetic peptide forms of these amino acids have been shown to affect crystal growth in precipitation of mineral crystals in solution. However, little is known about the effects of these peptides on the viability and phenotype of bone marrow stromal cells (BMSCs) or on the in vitro mineralization process. Bone marrow was harvested from neonatal rat femora and cultured under conditions to induce mineralized nodule formation. Mineralized bone nodules were grown while supplementing the cultures with one of five polyelectrolytes: polystyrene sulfonate (PSS), poly-L: -glutamic acid (PLG), poly-L: -lysine (PLL), poly-L: -aspartic acid (PLA), and sodium citrate (SC), as well as a nontreated control group. The viability and the rate of collagen synthesis under the effect of these agents were characterized by cell-counting and dye-binding assays, respectively. Raman microspectroscopy was conducted on mineralized bone nodules to determine the effect of the polyelectrolytes on the mineralization, type-B carbonation, and crystallinity of the mineral phase. Morphology of resulting mineral crystals was investigated using X-ray diffraction line-broadening analysis (XRD). PSS had toxic effects on cells whereas the remaining agents were biocompatible, as the cell viability was either greater (PLG) or not different from controls. The total collagen production by day 21 was 27% and 42% lower than controls for PLL and PSS, respectively. Culture wells stained positively for alkaline phosphatase in the presence of polyelectrolytes, indicating that osteogenic differentiation was not impacted negatively. Raman microspectroscopy revealed that the type-B carbonation of the crystal lattice increased when treated with PLG, PLL, or PSS. Crystallinity of PLL and PSS was smaller than that of control. The mineral/matrix ratios of nodules did not change with polyelectrolyte treatment, with the exception of the PSS-treated group, which was less mineralized. XRD analysis of bone nodules indicated that PLA-treated samples were significantly longer than controls along the 002 direction. Overall, the results suggest that the polypeptides consisting of charged amino acids are biocompatible and that they have the potential to affect crystal quality and morphology in vitro in the presence of cells. However, the mechanisms by which these effects come into play remain to be investigated.
Katherine L Dziak; Ozan Akkus
Related Documents :
17199476 - Micromorphological analysis of dentinal structure after irradiation with nd:yag laser a...
19024256 - Self-limiting caries therapy with proteolytic agents.
529046 - Sustained drug delivery systems ii: factors affecting release rates from poly(epsilon-c...
1380926 - The jasmonate precursor, 12-oxo-phytodienoic acid, induces phytoalexin synthesis in pet...
25302846 - High-yield synthesis of amido-functionalized polyoctahedral oligomeric silsesquioxanes ...
12830956 - Chemical destruction of mtbe using fenton's reagent: effect of ferrous iron/hydrogen pe...
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2008-11-01
Journal Detail:
Title:  Journal of bone and mineral metabolism     Volume:  26     ISSN:  0914-8779     ISO Abbreviation:  J. Bone Miner. Metab.     Publication Date:  2008  
Date Detail:
Created Date:  2008-11-03     Completed Date:  2008-12-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9436705     Medline TA:  J Bone Miner Metab     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  569-75     Citation Subset:  IM    
Department of Bioengineering, The University of Toledo, Toledo, OH, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Alkaline Phosphatase / metabolism
Bone Marrow Cells / metabolism
Calcification, Physiologic / physiology*
Cell Survival
Collagen / metabolism
Minerals / metabolism*
Peptides / metabolism*
Stromal Cells / metabolism
Reg. No./Substance:
0/Electrolytes; 0/Minerals; 0/Peptides; 9007-34-5/Collagen; EC Phosphatase

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

Previous Document:  Insufficient renal 1-alpha hydroxylase and bone homeostasis in aged rats with insulin resistance or ...
Next Document:  Potential involvement of p53 in ischemia/reperfusion-induced osteonecrosis.