EFFECTS OF WHEY-MILK PROTEINS ON CACO-2 AND HT-29 INTESTINAL-CELL LINES

Citation
B. Alstonmills et al., EFFECTS OF WHEY-MILK PROTEINS ON CACO-2 AND HT-29 INTESTINAL-CELL LINES, Livestock production science, 50(1-2), 1997, pp. 147-148
Citations number
NO
ISSN journal
03016226
Volume
50
Issue
1-2
Year of publication
1997
Pages
147 - 148
Database
ISI
SICI code
0301-6226(1997)50:1-2<147:EOWPOC>2.0.ZU;2-8
Abstract
The objective of this study was to determine whether alpha-lactalbumin (alpha-LA) and beta-lactoglobulin (beta-LG) affect proliferation of i ntestinal cells. As a consequence of intake of milk, epithelial cells of the intestine may be subjected to small concentrations of undergrad ed milk proteins. The question was whether alpha-LA or beta-LG have gr owth promoting or inhibiting properties in the intestinal epithelial c ell model systems, Caco-2 and HT-29. Cells were grown as recommended b y ATCC. Native bovine alpha-LA, or 2 and 4% trypsin hydrolyzed alpha-L A were added to cultures of Caco-2 cells in dosages of 0 to 50 ng/mL. After 24 to 120 h of culture, cell proliferation assays were done. By using the XTT cell proliferation assay, by visually counting cells in selected microscope fields, and by counting trypsinized cell suspensio ns in a hemocytometer, alpha-LA consistently increased cell replicatio n rate with a peak response at approximately 20 ng/mL. For example, th e HTT assay showed 85% increased mitochondrial dehydrogenase activity in the 15 ng/ml treatment relative to control. Higher concentrations w ere either less effective or ineffective growth stimulators in both ce ll lines. At 2% alpha-LA hydrolysis, there was a slight stimulation (7 %) and no effect at 4% hydrolysis. There was no response using bovine beta-LG as supplement. Variance from plating to plating was high, but percent changes from dose to dose within a plate were consistent over the replicates (C.V. < 5%). These data suggest that concentrations of alpha-LA that might escape digestion could alter the rate of prolifera tion or maturation of intestinal cells. We have not yet determined the mechanism for the alpha-LA effect. Published by Elsevier Science B.V.