Co-culture comprised of cryopreserved primary mouse hepatocytes cultured with cells of non-parenchymal, stromal type.
Example Metabolic Activity (nmoles/hr/106 cells)
| Substrate | Enzyme | Concentration (µM) | Day 1 | Day 4 | Day 8 |
| 7-Ethoxycoumarin | Phase I | 100 | 0.034 | 0.017 | 0.016 |
| 7-Hydroxycoumarin | Phase II | 100 | 51.5 | 46.5 | 0.21 |
| 7-Hydroxycoumarin | Phase II | 100 | 1.76 | 1.02 | 0.08 |
Culture Condition and Morphology
Cryopreserved primary mouse hepatocytes were thawed and plated with HUREL PlatinumHeps™ Media supplemented with 10% serum and subsequently changed 24 hours post-seeding to HUREL PlatinumHeps™ Basal Media. CYP substrate concentrations are given in the table above along with metabolite formation recorded as nmoles/hr/106 cells. All incubations were carried out in triplicate on days D1, D4, and D8 upon cell delivery and incubated for 60 minutes. Reactions took place in a humidified incubator at 37°C, in 5% CO2. Collected supernatants were stored at -20°C until further LC/MS/MS analysis
Day 1 – Morphology
Day 7 – Morphology
Day 7 – Bile Canaliculi
Phase contrast image in a 24-well at a 10x magnification.
Phase contrast image in a 24-well at a 10x magnification.
Bile canaliculi assayed via 5-(and-6)-carboxy-2’, 7’-dichlorofluorescein diacetate (C-DCFDA) stain at a concentration of 5 µM and imaged in the GFP channel in a 96-well at 10x magnification with filters EX/EM 492-495/512-527 nm.
Example Culture Origin
Animal Donor Demographics
- Strain: CD-1
- Number of Donors: 5
- Age(yrs)
- Sex: Male