Induction of HL‐60 cell differentiation by carotenoids

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Abstract
Recent observations indicated that carotenoids affected the proliferation and differentiation of certain cell lines. In the current experiments, beta-carotene and lutein were tested for the induction of differentiation with HL-60 cells, a bipotent promyelocytic leukemia cell line. Cultures were incubated with lutein (0.0-10.0 mumol/l), beta-carotene (0.0-10.0 mumol/l), and retinoic acid (0.0-1.0 mumol/l); retinoic acid incubations were positive controls for the differentiation of HL-60 cells into granulocytes. The carotenoid-incubated cultures developed significantly more (p < or = 0.05) differentiated cells than control cultures (vehicle alone). Morphology of the carotenoid-incubated cells indicated differentiation along the granulocytic pathway. The percentage of differentiated cells increased significantly throughout a seven-day incubation period to 25% (lutein), 35% (beta-carotene), and 75% (retinoic acid). A dose response was found for lutein (0.0-10.0 mumol/l), but not for beta-carotene. Throughout the incubation period, the percentage of differentiated cells in negative control cultures did not change, remaining at the initial background level (approximately 5%). These results provide evidence for carotenoid-induced differentiation of cells. Induction of cell differentiation by a carotenoid without (lutein) and with (beta-carotene) vitamin A activity suggested a vitamin A-independent mode of action for carotenoids in cell differentiation.