TY - JOUR
T1 - Human intestinal and lung cell lines exposed to beta-carotene show a large variation in intracellular levels of beta-carotene and its metabolites
AU - van Franssen-Hal, N.L.W.
AU - Bunschoten, J.E.
AU - Venema, D.P.
AU - Hollman, P.C.H.
AU - Riss, G.
AU - Keijer, J.
PY - 2005
Y1 - 2005
N2 - Although in vitro models are often used in ß-carotene research, knowledge about the uptake and metabolism of ß-carotene in cell lines is lacking. We measured by HPLC the intracellular levels of ß-carotene and its metabolites in 9 human intestinal and lung cell lines after exposure to 1 ¿M ß-carotene during 2, 6, 30, 54 h, and 3 weeks. In three colorectal carcinoma cell lines only low levels of ß-carotene could be detected and an apparent linear increase in intracellular ß-carotene was observed during the whole exposure period of 3 weeks. The remaining cell lines (an SV40 transformed colon cell line, a small intestinal carcinoma cell line and several lung cell lines) had medium or high intracellular ß-carotene levels. In these cell lines intracellular ß-carotene quickly increased during the first 54 h of exposure and after 3 weeks no further increase was observed, suggesting a stable level of ß-carotene after 54 h. Estimated intracellular concentrations at steady-state levels varied between 2 and 5 ¿M (low) or 9 and 55 ¿M (medium/high). Our results seem to indicate that an active uptake mechanism of ß-carotene exists in at least a subset of cell lines. Seven different ß-carotene metabolites were detected in the various cell lines (cis-carotene, retinol, three epoxy-carotenes, and two retinyl esters). Metabolite levels were the highest in cells with medium or high ß-carotene levels. Each cell line appeared to have a distinct metabolite profile. No intestinal or lung specific pattern could be found, but two epoxy-carotene metabolites were not detectable in the colon cell lines
AB - Although in vitro models are often used in ß-carotene research, knowledge about the uptake and metabolism of ß-carotene in cell lines is lacking. We measured by HPLC the intracellular levels of ß-carotene and its metabolites in 9 human intestinal and lung cell lines after exposure to 1 ¿M ß-carotene during 2, 6, 30, 54 h, and 3 weeks. In three colorectal carcinoma cell lines only low levels of ß-carotene could be detected and an apparent linear increase in intracellular ß-carotene was observed during the whole exposure period of 3 weeks. The remaining cell lines (an SV40 transformed colon cell line, a small intestinal carcinoma cell line and several lung cell lines) had medium or high intracellular ß-carotene levels. In these cell lines intracellular ß-carotene quickly increased during the first 54 h of exposure and after 3 weeks no further increase was observed, suggesting a stable level of ß-carotene after 54 h. Estimated intracellular concentrations at steady-state levels varied between 2 and 5 ¿M (low) or 9 and 55 ¿M (medium/high). Our results seem to indicate that an active uptake mechanism of ß-carotene exists in at least a subset of cell lines. Seven different ß-carotene metabolites were detected in the various cell lines (cis-carotene, retinol, three epoxy-carotenes, and two retinyl esters). Metabolite levels were the highest in cells with medium or high ß-carotene levels. Each cell line appeared to have a distinct metabolite profile. No intestinal or lung specific pattern could be found, but two epoxy-carotene metabolites were not detectable in the colon cell lines
KW - lecithin-retinol acyltransferase
KW - beta,beta-carotene 15,15'-dioxygenase
KW - excentric cleavage
KW - in-vitro
KW - vitamin
KW - acid
KW - expression
KW - oxidation
KW - enzymes
KW - ferret
U2 - 10.1016/j.abb.2005.05.001
DO - 10.1016/j.abb.2005.05.001
M3 - Article
VL - 439
SP - 32
EP - 41
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
SN - 0003-9861
IS - 1
ER -