Transport properties are not altered across Caco-2 cells with heightened TEER despite underlying physiological and ultrastructural changes

被引:60
作者
Lu, S
Gough, AW
Bobrowski, WF
Stewart, BH
机构
[1] WARNER LAMBERT PARKE DAVIS, PHARMACEUT RES DIV, DEPT PHARMACOKINET DRUG METAB, ANN ARBOR, MI 48105 USA
[2] WARNER LAMBERT PARKE DAVIS, PHARMACEUT RES DIV, DEPT PATHOL EXPTL TOXICOL, ANN ARBOR, MI 48105 USA
关键词
D O I
10.1021/js950269u
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Selected properties of Caco-2 cells were examined after disparate transepithelial electrical resistance (TEER) measurements were observed in two populations of Caco-2 cells. Comparisons were made between the early passages of Caco-2 cells (Caco-2E, passages 35-47) and the later passages of cells (Caco-2L, passages 87-112). Transmission electron microscopy revealed that regions of Caco-2L cells were composed of multiple cell layers rather than the monolayers observed in Caco-2E cells. Epithelial cell height (or barrier thickness) was not significantly different between the two cell populations. Intercellular and intracellular lumina were observed in the Caco-2L cells, but not in the Caco-2E cells. Results of [H-3]thymidine incorporation assays showed significantly higher cell proliferation rates in Caco-2L cells relative to Caco-2E cells. Despite morphological and physiological changes, there were no significant differences in the apparent permeabilities for D-mannitol (paracellular diffusion marker), hydrocortisone (transcellular diffusion marker), or dipeptide, Gly-Sar (carrier-mediated transcellular transport marker) between the two populations of cells. The higher TEER values in Caco-2L cells may be the result of a slight perturbation of tight junctions associated with both the multiple cell layers and the presence of intercellular lumina.
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页码:270 / 273
页数:4
相关论文
共 21 条
[1]   CORRELATION BETWEEN ORAL-DRUG ABSORPTION IN HUMANS AND APPARENT DRUG PERMEABILITY COEFFICIENTS IN HUMAN INTESTINAL EPITHELIAL (CACO-2) CELLS [J].
ARTURSSON, P ;
KARLSSON, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (03) :880-885
[2]   SELECTIVE PARACELLULAR PERMEABILITY IN 2 MODELS OF INTESTINAL-ABSORPTION - CULTURED MONOLAYERS OF HUMAN INTESTINAL EPITHELIAL-CELLS AND RAT INTESTINAL SEGMENTS [J].
ARTURSSON, P ;
UNGELL, AL ;
LOFROTH, JE .
PHARMACEUTICAL RESEARCH, 1993, 10 (08) :1123-1129
[3]   EPITHELIAL TRANSPORT OF DRUGS IN CELL-CULTURE .1. A MODEL FOR STUDYING THE PASSIVE DIFFUSION OF DRUGS OVER INTESTINAL ABSORPTIVE (CACO-2) CELLS [J].
ARTURSSON, P .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (06) :476-482
[4]   EPITHELIAL TRANSPORT OF DRUGS IN CELL-CULTURE .2. EFFECT OF EXTRACELLULAR CALCIUM-CONCENTRATION ON THE PARACELLULAR TRANSPORT OF DRUGS OF DIFFERENT LIPOPHILICITIES ACROSS MONOLAYERS OF INTESTINAL EPITHELIAL (CACO-2) CELLS [J].
ARTURSSON, P ;
MAGNUSSON, C .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1990, 79 (07) :595-600
[5]   THE USE OF CULTURED EPITHELIAL AND ENDOTHELIAL-CELLS FOR DRUG TRANSPORT AND METABOLISM STUDIES [J].
AUDUS, KL ;
BARTEL, RL ;
HIDALGO, IJ ;
BORCHARDT, RT .
PHARMACEUTICAL RESEARCH, 1990, 7 (05) :435-451
[6]   PROTEASE INHIBITORS SUPPRESS THE FORMATION OF TIGHT JUNCTIONS IN GASTROINTESTINAL CELL-LINES [J].
BACHER, A ;
GRIEBL, K ;
MACKAMUL, S ;
MITREITER, R ;
MUCKTER, H ;
BENSHAUL, Y .
EXPERIMENTAL CELL RESEARCH, 1992, 200 (01) :97-104
[7]   UPTAKE OF THE CEPHALOSPORIN, CEPHALEXIN, BY A DIPEPTIDE TRANSPORT CARRIER IN THE HUMAN INTESTINAL-CELL LINE, CACO-2 [J].
DANTZIG, AH ;
BERGIN, L .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1027 (03) :211-217
[8]   VITAMIN-B12 TRANSPORT THROUGH POLARIZED MONOLAYERS OF A COLON-CARCINOMA CELL-LINE [J].
DIX, CJ ;
OBRAY, HY ;
HASSAN, IF ;
WILSON, G .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1987, 15 (03) :439-440
[9]  
EKHATO IV, 1993, J LABELLED COMP RADI, V34, P107
[10]  
HIDALGO IJ, 1989, GASTROENTEROLOGY, V96, P736