<p>The majority of H<sub>2</sub>O<sub>2</sub> -treated cells were already detached and floating (b, asterisk), whereas control and B3-treated cells had started rounding but mostly remained adherent (c, d, asterisk). Scale bar = 200 µm. Cell viability of chondrocytes treated with H<sub>2</sub>O<sub>2</sub> and B3 as determined by the LDH assay (e). B3 prevented H<sub>2</sub>O<sub>2</sub>-induced chondrocyte apoptosis in a dose-dependent manner. Values represent the mean and SD; n = 5 samples/group. *<i>p</i><0.05.</p
Proliferation differentiation and apoptosis rate of fibroblast and chondrocytes chondrocytes were pr...
Chondrocytes at the lower zone of the growth plate must be eliminated to facilitate longitudinal gro...
Cells were treated as in Fig 6, then cell viability was estimated after 24 h or 72 h. * p ≤ 0.05, si...
<p>A-J: Serum-starved human primary chondrocytes (Ch) were cultured to sub-confluence in monolayer c...
<p>Chondrocytes were pretreated with or without specific inhibitors for 1 h and then incubated under...
<p>(A) TUNEL-positive cells (green fluorescence) were observed under a fluorescence microscope. (B) ...
<p>Confocal fluorescent images of chondrocytes treated with media <b>(A)</b>, 5 mM acrylamide for 16...
<p>Monolayer cultures of OA chondrocytes, pre-treated with or without HT for 30 min, were incubated ...
<p><b>(a).</b> Chondrocytes identified by toluidine blue staining. <b>(b).</b> Aggrecan staining (Pr...
<p>(a, b) B3 prevents H<sub>2</sub>O<sub>2</sub>- (a) or IL-1β(b)-induced iNOS synthesis. Primary ch...
<p>Transmission electron microscopy was performed to study the effects of IGF-1 or/and PDGF-bb on IL...
<p><b>A)</b> Representative micrographs of apoptosis in tibia growth plate cartilage on day 13 in ve...
<p>The data are shown as the mean ±S.D. a, b, c and d show cell proliferation in each group compared...
<p>(A1–A3) Control chondrocytes. (B1–B3) Chondrocytes treated with 1.5 mM SNP for 12 h. (C1–C3) The ...
<p>(A-C) Human chondrocytes were cultured on a positive control substrate (Ctrl), on gelatin gel (g ...
Proliferation differentiation and apoptosis rate of fibroblast and chondrocytes chondrocytes were pr...
Chondrocytes at the lower zone of the growth plate must be eliminated to facilitate longitudinal gro...
Cells were treated as in Fig 6, then cell viability was estimated after 24 h or 72 h. * p ≤ 0.05, si...
<p>A-J: Serum-starved human primary chondrocytes (Ch) were cultured to sub-confluence in monolayer c...
<p>Chondrocytes were pretreated with or without specific inhibitors for 1 h and then incubated under...
<p>(A) TUNEL-positive cells (green fluorescence) were observed under a fluorescence microscope. (B) ...
<p>Confocal fluorescent images of chondrocytes treated with media <b>(A)</b>, 5 mM acrylamide for 16...
<p>Monolayer cultures of OA chondrocytes, pre-treated with or without HT for 30 min, were incubated ...
<p><b>(a).</b> Chondrocytes identified by toluidine blue staining. <b>(b).</b> Aggrecan staining (Pr...
<p>(a, b) B3 prevents H<sub>2</sub>O<sub>2</sub>- (a) or IL-1β(b)-induced iNOS synthesis. Primary ch...
<p>Transmission electron microscopy was performed to study the effects of IGF-1 or/and PDGF-bb on IL...
<p><b>A)</b> Representative micrographs of apoptosis in tibia growth plate cartilage on day 13 in ve...
<p>The data are shown as the mean ±S.D. a, b, c and d show cell proliferation in each group compared...
<p>(A1–A3) Control chondrocytes. (B1–B3) Chondrocytes treated with 1.5 mM SNP for 12 h. (C1–C3) The ...
<p>(A-C) Human chondrocytes were cultured on a positive control substrate (Ctrl), on gelatin gel (g ...
Proliferation differentiation and apoptosis rate of fibroblast and chondrocytes chondrocytes were pr...
Chondrocytes at the lower zone of the growth plate must be eliminated to facilitate longitudinal gro...
Cells were treated as in Fig 6, then cell viability was estimated after 24 h or 72 h. * p ≤ 0.05, si...