MATURATIONAL CHANGES INDUCED BY 1-ALPHA,25-DIHYDROXYVITAMIN-D(3) IN TYPE-II CELLS FROM FETAL-RAT LUNG EXPLANTS

Specific binding sites for la,25 dihydroxyvitamin D3 [1alpha,25-(OH)2D 3] localized to type II pneumocytes have been evidenced in fetal rat l ung at the end of gestation, suggesting a role for vitamin D3 in the c ontrol of lung maturation. In this study, we describe the morphologica l changes that occur in lung explants from 18-day-old rat fetuses grow n for 1 and 2 days in control conditions and in the presence of 1alpha ,25(OH)2D3 (10(-9) M) or dexamethasone (10(-7) M). Point Counting and planimetric measurements on light and electron micrographs show that 1 alpha,25-(OH)2D3 1) dramatically decreases the mean glycogen content o f type II cell profiles between days 1 and 2 of the culture, suggestin g an acceleration of the glycogenolytic processes normally occuring at that stage and 2) does not change the intracellular osmiophilic lamel lar body (OLB) content of cell profiles, but increases the amount of i ntraluminal sufactant by 126% when expressed as surfactant clusters su rface area/section sur face area and by 129% when expressed on a per c ell basis, suggesting a stimulation of surfactant synthesis and secret ion. By contrast, dexamethasone, increases the mean intracellular OLB content of type II cell profiles by 306% and decreases the relative su rface area of secreted material by 53 and 73%. In conclusion, 1alpha,2 5(OH)2D3 accelerates the physiological maturation of fetal rat type II pneumocytes and could represent a key factor for the onset of normal lung function at birth.