DIFFERENTIAL MODULATION OF CHICKEN LYMPHOCYTE BLASTOGENESIS AND CYTOTOXIC ACTIVITY OF NATURAL-KILLER-CELLS IN-VITRO BY RETINOL, RETINOIC ACID AND BETA-CAROTENE
M. Lessard et M. Dupuis, DIFFERENTIAL MODULATION OF CHICKEN LYMPHOCYTE BLASTOGENESIS AND CYTOTOXIC ACTIVITY OF NATURAL-KILLER-CELLS IN-VITRO BY RETINOL, RETINOIC ACID AND BETA-CAROTENE, Nutrition research, 14(8), 1994, pp. 1201-1217
The effects of retinol (ROL), retinoic acid (RA) and beta-carotene (CA
R) on the response of chicken lymphocyte blastogenesis and on the cyto
toxic activity of natural killer (NK) cells were evaluated in vitro. S
plenocytes were isolated from healthy growing chicks and cultured in p
resence of different concentrations of ROL, RA and CAR under similar e
xperimental conditions. Lymphocyte response to concanavalin A (Con A)
was affected by adding ROL, RA and CAR to the cultures, by the time of
exposure and by methods used for diluting ROL, RA and CAR stock solut
ions. Addition of ROL stock solutions diluted in cell culture medium s
uppressed lymphocyte response in a linear dose-dependent manner wherea
s pre-dilution of ROL stock solutions in fetal bovine serum (ROL-FBS)
increased blastogenesis in a linear manner. Addition of 10 mu M of ROL
-FBS at the beginning of the incubation period or 16 h after enhanced
proliferative responses by 5 and 9 times, respectively, as compared to
Con A-induced cells without ROL. Suppressed proliferative response of
Con A-induced cells was seen when both RA and CAR working solutions w
ere added at a concentration of 10 mu M and 1 mu M, respectively. Howe
ver, RA and CAR pre-diluted in FBS (RA-FBS, CAR-FBS) increased prolife
rative response of Con A-induced cells in a quadratic dose-dependent m
anner. At peak levels of RA-FBS and CAR-FBS, blastogenesis was respect
ively 2.1 and 1.3 times higher than activated cells without RA-FBS or
CAR-FBS. No significant increase was detected with RA or CAR directly
diluted in RPMI medium. Cytotoxic activity of chicken NK cells was red
uced when ROL was added to the cultures, whereas RA and CAR enhanced N
K activity. Both preparations of tested compounds had similar effects
on NK activity. Our results showed that immunocompetent cell functions
were modulated by retinol, retinoic acid and beta-carotene ina dose-d
ependent manner and by the method used to prepare the working solution
s.