pASARM and npASARM peptides were added to ATDC5 cells and metatarsal organ cultures at concentrations Selleck Navitoclax of 10, 20 and 50 μM, with controls treated with a DMSO (Sigma) carrier only. In further studies, peptides were added at a final concentration of 20 μM with experiments being performed at least 3 times. Embryonic metatarsal organ cultures provide a well‐established model of endochondral bone growth [22], [23] and [24]. Metatarsal bones were cultured in a humidified atmosphere

(37 °C, 5% CO2) in 24-well plates for up to 10 days. Each culture well contained 300 μl α-minimum essential medium (MEM) supplemented with 0.2% BSA Fraction V; 1 mmol/l β-glycerophosphate (βGP); 0.05 mg/ml L-ascorbic acid phosphate; 0.05 mg/ml gentamicin and 1.25 μg/ml fungizone (Invitrogen, Paisley, UK) as previously described [22]. For the E17 bones, the medium was changed every second or third day and for the E15 bones, the medium was not changed throughout the culture period [25]. Concentrations of peptide and DMSO carrier were however added every second day. The total length of the bone through the centre of the mineralizing zone was determined using image analysis software (DS Camera Control Unit DS-L1; Nikon) every second or third

day. ICG-001 in vitro The length of the central mineralization zone was also measured. All results are expressed as a percentage change from harvesting length which was regarded as baseline. Metatarsals were fixed in 70% ethanol, stained with eosin dye (for visualisation) and then embedded in paraffin blocks. Samples were then were scanned

with a high-resolution μCT (μCT40; Scanco Medical, Southeastern, PA) as previously described [13] and [16]. Data were acquired at 55 KeV with 6 μm cubic voxels. Three-dimensional reconstructions for bone samples were generated with the following parameters: Gauss Sigma = 4.0; Support = 2, Lower Threshold = 90 and Upper Threshold = 1000. Tissue mineral density was derived from the linear attenuation coefficient of threshold bone through precalibration of the apparatus for the acquisition voltage chosen. The Methocarbamol bone volume (BV/TV) was measured using sections encompassing the entire metatarsal on a set of 85 sections that was geometrically aligned for each sample. On day 7 of culture, 3 μCi/ml [3H]-thymidine (Amersham Biosciences, Little Chalfont, UK) was added to each metatarsal for the last 6 h of culture [22]. After washing in PBS, the unbound thymidine was extracted using 5% trichloroacetic acid (Sigma). Metatarsals were then washed in PBS before being solubilised (NCS-II tissue solubiliser, 0.5 N, Amersham) at 60 °C for 1 h. [3H]-thymidine incorporated into DNA was determined using a scintillation counter.