Genetically Modified Caco-2 Cells With Improved Cytochrome P450 Metabolic Capacity

被引:26
作者
Kublbeck, Jenni [1 ]
Hakkarainen, Jenni J. [1 ]
Petsalo, Aleksanteri [1 ]
Vellonen, Kati-Sisko [1 ]
Tolonen, Ari [2 ]
Reponen, Petri [3 ]
Forsberg, Markus M. [1 ]
Honkakoski, Paavo [1 ]
机构
[1] Univ Eastern Finland, Sch Pharm, FI-70211 Kuopio, Finland
[2] Admescope Ltd, Typpitie 1, FI-90620 Oulu, Finland
[3] Novamass Ltd, Viikinkaari 4, FI-00790 Helsinki, Finland
关键词
Caco-2; cells; cytochrome P450; metabolism; nuclear receptors; permeability; transporters; RESPONSIVE ENHANCER MODULE; MESSENGER-RNA-EXPRESSION; BLOOD-BRAIN-BARRIER; VITAMIN-D-RECEPTOR; NUCLEAR RECEPTORS; GENE-EXPRESSION; P-GLYCOPROTEIN; DRUG TRANSPORT; UP-REGULATION; MODEL SYSTEM;
D O I
10.1016/S0022-3549(15)00187-2
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The human intestinal Caco-2 cell line has been extensively used as a model of small intestinal absorption but it lacks expression and function of cytochrome P450 enzymes, particularly CYP3A4 and CYP2C9, which are normally expressed in the intestinal epithelium. In order to increase the expression and activity of CYP isozymes in these cells, we created 2 novel Caco-2 sublines expressing chimeric constitutive androstane or pregnane X receptors and characterized these cells for their metabolic and absorption properties. In spite of elevated mRNA expression of transporters and differentiation markers, the permeation properties of the modified cell lines did not significantly differ from those of the wild-type cells. In contrast, the metabolic activity was increased beyond the currently used models. Specifically, CYP3A4 activity was increased up to 20-fold as compared to vitamin D treated wild-type Caco-2 cells. (C) 2016 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:941 / 949
页数:9
相关论文
共 42 条
  • [1] Low Levels of GSTA1 Expression Are Required for Caco-2 Cell Proliferation
    Adnan, Humaira
    Quach, Holly
    MacIntosh, Kimberley
    Antenos, Monica
    Kirby, Gordon M.
    [J]. PLOS ONE, 2012, 7 (12):
  • [2] Intestinal drug absorption and metabolism in cell cultures: Caco-2 and beyond
    Artursson, P
    Borchardt, RT
    [J]. PHARMACEUTICAL RESEARCH, 1997, 14 (12) : 1655 - 1658
  • [3] Caco-2 monolayers in experimental and theoretical predictions of drug transport (Reprinted from Advanced Drug Delivery Reviews, vol 22, pg 67-84, 1996)
    Artursson, P
    Palm, K
    Luthman, K
    [J]. ADVANCED DRUG DELIVERY REVIEWS, 2001, 46 (1-3) : 27 - 43
  • [4] Functionally conserved xenobiotic responsive enhancer in cytochrome P450 3A7
    Bertilsson, G
    Berkenstam, A
    Blomquist, P
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (01) : 139 - 144
  • [5] Characterizing the expression of CYP3A4 and efflux transporters (P-gp, MRP1, and MRP2) in CYP3A4-transfected Caco-2 cells after induction with sodium butyrate and the phorbol ester 12-O-tetradecanoylphorbol-13-acetate
    Cummins, CL
    Mangravite, LM
    Benet, LZ
    [J]. PHARMACEUTICAL RESEARCH, 2001, 18 (08) : 1102 - 1109
  • [6] CYP3A4, CYP3A5, and MDR1 in human small and large intestinal cell lines suitable for drug transport studies
    Engman, HA
    Lennernäs, H
    Taipalensuu, J
    Otter, C
    Leidvik, B
    Artursson, P
    [J]. JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (11) : 1736 - 1751
  • [7] Up-Regulation of Transporters and Enzymes by the Vitamin D Receptor Ligands, 1α,25-Dihydroxyvitamin D3 and Vitamin D Analogs, in the Caco-2 Cell Monolayer
    Fan, Jianghong
    Liu, Shanjun
    Du, Yimin
    Morrison, Jodi
    Shipman, Robert
    Pang, K. Sandy
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2009, 330 (02) : 389 - 402
  • [8] In vitro models for the blood-brain barrier
    Garberg, P
    Ball, M
    Borg, N
    Cecchelli, R
    Fenart, L
    Hurst, RD
    Lindmark, T
    Mabondzo, A
    Nilsson, JE
    Raub, TJ
    Stanimirovic, D
    Terasaki, T
    Öberg, JO
    Österberg, T
    [J]. TOXICOLOGY IN VITRO, 2005, 19 (03) : 299 - 334
  • [9] The orphan human pregnane X receptor mediates the transcriptional activation of CYP3A4 by rifampicin through a distal enhancer module
    Goodwin, B
    Hodgson, E
    Liddle, C
    [J]. MOLECULAR PHARMACOLOGY, 1999, 56 (06) : 1329 - 1339
  • [10] EFFECTS OF 1,25-DIHYDROXYVITAMIN-D(3) ON PROLIFERATION AND DIFFERENTIATION OF CACO-2 CELLS
    HALLINE, AG
    DAVIDSON, NO
    SKAROSI, SF
    SITRIN, MD
    TIETZE, C
    ALPERS, DH
    BRASITUS, TA
    [J]. ENDOCRINOLOGY, 1994, 134 (04) : 1710 - 1717