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AIM:To investigate whether the secretion of phospha-tidylcholine(PC)in intestinal mucus occurs by apical secretion or via basolateral excretion and to determine its subsequent passage across the tight junctions to the apical mucus.METHODS:We addressed this question using the po-larized intestinally differentiated tumor cell line CaCo-2 grown on filters to confluence in Transwell culture chambers.The released PC and sphingomyelin(Sph)from apical and basolateral media were analyzed by mass spectrometry.RESULTS:The secreted PC species were identical in both compartments indicating the same intracellular origin of PC.However,PC secretion into the basolateral compart-ment was more effective,and the PC:Sph ratio in the ba-solateral compartment was signif icantly higher than that in the apical compartment(8.18 ± 1.84 vs 4.31 ± 1.22,P = 0.01).Both pathways were temperature sensitive and were unaltered in the presence of cyclosporine.CONCLUSION:The data demonstrate the PC secre-tion capacity of CaCo-2 cells and indicate two sepa-rated apical and basolateral release mechanisms.
AIM: To investigate whether the secretion of phosphatidylcholine (PC) in intestinal mucus occurs by apical secretion or via basolateral excretion and to determine its subsequent passage across the tight junctions to the apical mucus. METHODS: We addressed this question using the po- larized intestinally differentiated tumor cell line CaCo-2 grown on filters to confluence in Transwell culture chambers. released PC and sphingomyelin (Sph) from apical and basolateral media were analyzed by mass spectrometry .RESULTS: The secreted PC species were identical in both compartments indicating the same intracellular origin of PC.However, PC secretion into the basolateral compart- ment was more effective, and the PC: Sph ratio in the ba-solateral compartment was signif icantly higher than that in the apical compartment (8.18 ± 1.84 vs. 4.31 ± 1.22, P = 0.01) .Both pathways were temperature sensitive and were unaltered in the presence of cyclosporine. CONCLUSION: The data demonstrates the PC secrecy capacity of CaCo-2 cells and two separated-rated apical and basolateral release mechanisms.