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Higher expression of cytochrome P450 3A4 in human mesenchymal and adipose-derived stem cells than in dermal fibroblasts: With emphasis on the correlation with basal pregnane X receptor expression
- Source :
- Process Biochemistry. 49:1983-1989
- Publication Year :
- 2014
- Publisher :
- Elsevier BV, 2014.
-
Abstract
- Among the cytochrome P 450 (CYP) enzymes, CYP3A4 is most abundantly existed and metabolizes most of the drugs. We have shown human dermal fibroblasts (HDFs) express low levels of CYPs, but could be engineered to express much higher levels to be used as drug metabolism prediction. To seek better cell source for engineering, the basal mRNA expression and enzyme activities of CYP3A4 in HDFs ( n = 5), bone marrow-derived mesenchymal stem cells (BMMSCs, n = 7), and adipose-derived stem cells (ADSCs, n = 3) were compared. The basal CYP3A4 expression and activity in BMMSCs and ADSCs were significantly higher than in HDFs. However, the coefficient of variation of CYP3A4 expression was very high in each cell type. Comparing the expression levels of 4 regulators glucocorticoid receptor, pregnane X receptor ( PXR ), hepatocyte nuclear factor 4α, and hydrocarbon receptor nuclear translocator in the total 15 cell samples, we found the only basal PXR expression was significantly correlated with CYP3A4 expression. The gender and age of patients were not significant determinants in the expressions of PXR and CYP3A4 . In conclusion, BMMSCs and ADSCs expressed higher levels of CYP3A4 than HDFs and the expression of CYP3A4 might be mainly determined by basal PXR expression.
- Subjects :
- Pregnane X receptor
medicine.medical_specialty
CYP3A4
Pregnane
Cell
Mesenchymal stem cell
Bioengineering
Biology
Applied Microbiology and Biotechnology
Biochemistry
Molecular biology
chemistry.chemical_compound
medicine.anatomical_structure
Glucocorticoid receptor
Endocrinology
chemistry
Internal medicine
medicine
Stem cell
Receptor
Subjects
Details
- ISSN :
- 13595113
- Volume :
- 49
- Database :
- OpenAIRE
- Journal :
- Process Biochemistry
- Accession number :
- edsair.doi...........374e6c7f9b132af1b05f38c62bb3c5bc
- Full Text :
- https://doi.org/10.1016/j.procbio.2014.08.006