2011
DOI: 10.1016/j.biomaterials.2011.01.020
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Maintenance of phenotype and function of cryopreserved bone-derived cells

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Cited by 13 publications
(13 citation statements)
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“…The frozen bone chips were thawed and incubated with standard Dulbecco's modified Eagle's medium containing 10% (v/v) fetal bovine serum (Hyclone, Logan, UT, USA) after a prescribed 3 months of cryopreservation. The cell culture method was performed in accordance with a previous report . The medium was replaced every 3 to 4 days until cell density reached 70% to 80% confluence.…”
Section: Methodsmentioning
confidence: 99%
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“…The frozen bone chips were thawed and incubated with standard Dulbecco's modified Eagle's medium containing 10% (v/v) fetal bovine serum (Hyclone, Logan, UT, USA) after a prescribed 3 months of cryopreservation. The cell culture method was performed in accordance with a previous report . The medium was replaced every 3 to 4 days until cell density reached 70% to 80% confluence.…”
Section: Methodsmentioning
confidence: 99%
“…The cell culture method was performed in accordance with a previous report. 17 The medium was replaced every 3 to 4 days until cell density reached 70% to 80% confluence. After the first passage, the following three supplements were added: 100 nM dexamethasone, 0.05 mM ascorbic acid 2-phosphate, and 10 mM betaglycerophosphate.…”
Section: Cryopreservation and Cell Culturementioning
confidence: 99%
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“…Processes such as irradiation and freeze drying are used to decrease risks, but these procedures also eliminate the cellular component, resulting in reduced osteoinductivity [8]. Moreover, allogeneic bone has decreased revascularization and a higher resorption rate [2], resulting in a lower rate of new bone tissue formation as compared to autologous bone [8, 9]. Another alternative method is synthetic prostheses such as hydroxyapatite, beta-Tricalcium phosphate, and calcium phosphate cements.…”
Section: Introductionmentioning
confidence: 99%
“…The undecalcified specimens of 6 nude mice (4 specimens from each group) were processed following these steps: (1) dehydration in a graded series of ethanol from 75% to 100%; (2) embedding in polymethylmethacrylate (PMMA); (3) sectioning (150 mm thick) using a microtome (Leica, Hamburg, Germany); (4) polishing the sections to a final thickness of approximately 40 mm; and (5) staining the sections with Van Gieson's picrofuchsin [25]. Lastly, under an inverted microscope, sections were observed for new bone formation and remnant scaffolds.…”
Section: Methodsmentioning
confidence: 99%