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

J Pharm Sci

Department of Pharmacokinetics/Drug Metabolism, Parke-Davis Research Division, Warner-Lambert Company, Ann Arbor, MI 48105, USA.

Published: March 1996

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 [3H]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 results of a slight perturbation of tight junctions associated with both the multiple cell layers and the presence of intercellular lumina.

Download full-text PDF

Source
http://dx.doi.org/10.1021/js950269uDOI Listing

Publication Analysis

Top Keywords

caco-2 cells
16
caco-2l cells
16
cells
13
caco-2e cells
12
cells caco-2e
8
multiple cell
8
cell layers
8
diffusion marker
8
caco-2l
5
cell
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!