2010
DOI: 10.1016/j.actbio.2010.03.003
|View full text |Cite
|
Sign up to set email alerts
|

The resorption of nanocrystalline calcium phosphates by osteoclast-like cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
72
0

Year Published

2011
2011
2023
2023

Publication Types

Select...
6
2

Relationship

1
7

Authors

Journals

citations
Cited by 88 publications
(75 citation statements)
references
References 54 publications
3
72
0
Order By: Relevance
“…Interestingly, but in spite on the fact that the biological apatite of bones contains the substantial amount of carbonates, among investigated samples of nanocrystalline apatites, osteoclastic differentiation was found to be constrained on carbonate-rich samples, leading to smaller numbers of osteoclast-like cells and fewer resorption pits. Furthermore, the highest resorption rate was found for nanodimensional HA with a low carbonate content, which strongly stimulated the differentiation of osteoclast-like cells on its surface [674].…”
Section: Nanodimensional and Nanocrystalline Calcium Orthophosphates mentioning
confidence: 98%
“…Interestingly, but in spite on the fact that the biological apatite of bones contains the substantial amount of carbonates, among investigated samples of nanocrystalline apatites, osteoclastic differentiation was found to be constrained on carbonate-rich samples, leading to smaller numbers of osteoclast-like cells and fewer resorption pits. Furthermore, the highest resorption rate was found for nanodimensional HA with a low carbonate content, which strongly stimulated the differentiation of osteoclast-like cells on its surface [674].…”
Section: Nanodimensional and Nanocrystalline Calcium Orthophosphates mentioning
confidence: 98%
“…Resorption implies an initial tight attachment of osteoclasts to the disk surface to create the "sealing zone", rich in F-actin, which isolates the resorptive space from the surrounding material. 11,12 The ruffled border is formed by fusion of intracellular acidic vesicles which contain enzymes (such as cathepsin K), Cl − and H + ions which are released into the resorption lacunae for the acidification to a pH of around 4.5. [13][14][15] This process produces the dissolution of the material, which is then endocytosed from the resorption cavity and transported to the secretory domain for releasing into the extracellular environment.…”
Section: Intracellular Ros and Camentioning
confidence: 99%
“…The osteoclast thus isolates the resorptive space from the surrounding bone. 11,12 The ruffled border is formed by fusion of intracellular acidic vesicles which form finger-like projections inside the sealing zone. The vesicles contain a cocktail of matrix-degrading enzymes (such as cathepsin K), hydrogen ions (H + ) and chloride ions (Cl − ) which are released into the resorption lacunae and are responsible for acidification to a pH of around 4.5.…”
Section: Introductionmentioning
confidence: 99%
“…U-937 and RAW 264.7 monocytic-macrophage leukemia cells, fibroblasts, endothelial cells and primary osteoclast progenitors have been carried out with several of the above bone substitute materials to not only assess osteoclast differentiation and osteoclast activity but also secretion of cellular factors [2]. Specifically, the RAW 264.7 murine leukemia cell line has been used as an important in vitro cell culture model for studying activation and differentiation into osteoclastlike cells [9,10]. For example, when RAW 264.7 cells were grown for 14 days on HAp and stimulated with RANKL, differentiation via cell fusion occurred into osteoclast-like multinucleated cells [9].…”
Section: Introductionmentioning
confidence: 99%
“…Specifically, the RAW 264.7 murine leukemia cell line has been used as an important in vitro cell culture model for studying activation and differentiation into osteoclastlike cells [9,10]. For example, when RAW 264.7 cells were grown for 14 days on HAp and stimulated with RANKL, differentiation via cell fusion occurred into osteoclast-like multinucleated cells [9]. Additionally, 3D cell culture scaffolds composed of biphasic calcium phosphate (BCP) biomaterial, human plasma clots, and RAW 264.7 cells stimulated for 2 days in the presence of a transfected overexpression vector containing a glutathione-S transferase (GST)-RANKL fusion protein demonstrated significantly increased expression of Vegfa and Vegfc compared to untreated controls [11].…”
Section: Introductionmentioning
confidence: 99%