Sato M, Hiragun A
Department of Oncology, Tokyo Metropolitan Institute of Medical Science, Japan.
J Cell Physiol. 1988 Jun;135(3):545-50. doi: 10.1002/jcp.1041350326.
The active metabolite of vitamin D3, 1 alpha,25-dihydroxyvitamin D3 (1,25(OH)2D3), inhibited morphologic and enzymatic expression during differentiation of preadipocyte to adipocyte. In the presence of approximately 6.4-20 X 10(-10) M 1,25(OH)2D3, the triacylglycerol accumulation was only 50% of that of fully differentiated control cells. High-affinity binding sites for 1,25-dihydroxyvitamin D3 were detected in two preadipose cell lines. The 1,25(OH)2D3 binding component sediments at 3.3 S in 4-24% (w/v) sucrose gradients prepared in hypertonic buffer. Binding assay revealed that Nmax was 70 fmol/mg protein and 90 fmol/mg protein, and Kd value was 170 pM and 37 pM in cell lines ST 13 and 3T3 L1, respectively. We also found that differentiated adipocytes did not contain specific receptors for 1,25(OH)2D3. 1,25(OH)2D3, 1(OH)D3, 24,25(OH)2D3, and 24(OH)D3 all suppressed differentiation of preadipocytes to adipocytes, and the dose required closely reflected the affinities of the various metabolites and the synthetic derivative for 1,25(OH)2D3 receptor. It is suggested that the action of vitamin D3 on preadipocyte differentiation may result from a receptor-mediated event.
维生素D3的活性代谢产物1α,25 - 二羟基维生素D3(1,25(OH)2D3)在脂肪前体细胞向脂肪细胞分化过程中抑制其形态和酶表达。在约6.4 - 20×10(-10) M的1,25(OH)2D3存在下,三酰甘油积累量仅为完全分化的对照细胞的50%。在两种脂肪前体细胞系中检测到1,25 - 二羟基维生素D3的高亲和力结合位点。在高渗缓冲液中制备的4 - 24%(w/v)蔗糖梯度中,1,25(OH)2D3结合成分在3.3 S处沉降。结合试验表明,在细胞系ST 13和3T3 L1中,Nmax分别为70 fmol/mg蛋白和90 fmol/mg蛋白,Kd值分别为170 pM和37 pM。我们还发现分化的脂肪细胞不含有1,25(OH)2D3的特异性受体。1,25(OH)2D3、1(OH)D3、24,25(OH)2D3和24(OH)D3均抑制脂肪前体细胞向脂肪细胞的分化,所需剂量密切反映了各种代谢产物和合成衍生物对1,25(OH)2D3受体的亲和力。提示维生素D3对脂肪前体细胞分化的作用可能是由受体介导的事件引起的。