2012
DOI: 10.1016/j.actbio.2011.12.024
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Karyotyping of human chondrocytes in scaffold-assisted cartilage tissue engineering

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Cited by 11 publications
(15 citation statements)
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“…In contrast, from another study, eight post-mortem specimens from old donors analyzed by GTG-banding showed high frequency of aneuploidies 8 . Predominantly loss of one gonosome and gains of chromosomes 5, 7, 8 and gonosomes were detected.…”
Section: Autosomal Stabilitymentioning
confidence: 67%
See 1 more Smart Citation
“…In contrast, from another study, eight post-mortem specimens from old donors analyzed by GTG-banding showed high frequency of aneuploidies 8 . Predominantly loss of one gonosome and gains of chromosomes 5, 7, 8 and gonosomes were detected.…”
Section: Autosomal Stabilitymentioning
confidence: 67%
“…Interestingly, all these aberrations were already present in the first passage directly after the establishment of the cell culture, suggesting their presence in the original cartilage tissue. In the same study, five samples from younger patients with cartilage damage showed mostly normal karyotypes with negligible single non-clonal events of numerical and structural aberrations 8 . These results are in concordance with past studies showing for a limited number of donors, that chondrocytes subjected to knee surgery showed a normal karyotype 9 and that even extensive expansion of the chondrocytes had no effect on chromosome number or structure 10 .…”
Section: Autosomal Stabilitymentioning
confidence: 72%
“…PGA is a synthetic polymer successfully used in cartilage tissue engineering for its biocompatibility and mechanical properties (Trimborn et al 2012).…”
Section: Introductionmentioning
confidence: 99%
“…93 We developed a 3D single cell culture system that exploits single 94 cell patterning with in situ matrix gelation, to create well-defined 95 was then employed to remove amino-groups on the exposed sur-113 face. A second surface modification of the exposed area was con- The cell suspension was 146 then adjusted to desirable seeding densities for different sized pat-147 terns, namely 2 Â 10 5 , 0.5 Â 10 5 and 0.2 Â 10 5 cells/ml for 20,40,148 and 80 lm micropatterns respectively. A patterned substrate was 149 then immersed in a cell suspension of appropriate density for 150 1-2 h, followed by removal of cell suspension and a gentle rinse 151 with fresh medium to remove loosely attached cells.…”
Section: Introductionmentioning
confidence: 99%
“…40, and 80 lm were prepared. The distance between two adja-253 cent circles was either 80 or 100 lm.…”
mentioning
confidence: 99%