Ottonello S, Petrucco S, Maraini G
J Biol Chem. 1987 Mar 25;262(9):3975-81.
We have investigated the steps by which retinol, released from plasma retinol-binding protein (RBP), enters the cells and is accumulated for the most part as a retinyl-ester, only a small fraction of it being present as a complex with cytoplasmic retinol-binding protein (CRBP). For this purpose, we have developed a cell-free system composed of plasma membrane-enriched fractions from bovine retinal pigment epithelium which selectively incorporates exogenous vitamin A when presented as a retinol-RBP complex. Upon incubation in the presence of [3H]retinol-RBP, isolated plasma membrane fractions take up and esterify retinol. A 4-fold reduction of total vitamin A incorporation is observed in conditions which specifically inhibit retinyl-ester formation, thus indicating that the two processes of retinol uptake and esterification are functionally coupled. Evidence is presented that retinol bound to a plasma membrane receptor sharing functional and structural similarities with CRBP is the actual substrate for esterification. Vitamin A accumulation seems to require retinol esterification to allow the recycling of a limited number of free, plasma membrane-associated, retinol receptors. Mobilization of retinol stored as a membrane-bound retinyl-ester is mediated by a membrane-associated hydrolase activity selectively controlled by the level of apo-CRBP which acts as a carrier for the released retinol. Up to 90% of membrane-bound vitamin A is released upon incubation in the presence of apo-CRBP (11 microM) with concomitant formation of retinol-CRBP. The overall process, in which retinol never needs to leave its binding proteins, allows the accumulation of vitamin A in the form of a membrane-bound retinyl-ester and its regulated mobilization as a retinol-CRBP complex.
我们研究了从血浆视黄醇结合蛋白(RBP)释放出来的视黄醇进入细胞并大部分以视黄酯形式积累的步骤,其中只有一小部分以与细胞质视黄醇结合蛋白(CRBP)形成的复合物形式存在。为此,我们开发了一种无细胞系统,该系统由来自牛视网膜色素上皮的富含质膜的部分组成,当以视黄醇-RBP复合物形式呈现时,该部分会选择性地摄取外源性维生素A。在[3H]视黄醇-RBP存在下孵育时,分离的质膜部分摄取并酯化视黄醇。在特异性抑制视黄酯形成的条件下,观察到总维生素A摄取量降低了4倍,这表明视黄醇摄取和酯化这两个过程在功能上是耦合的。有证据表明,与CRBP在功能和结构上具有相似性的与质膜受体结合的视黄醇是酯化的实际底物。维生素A的积累似乎需要视黄醇酯化,以允许有限数量的游离、与质膜相关的视黄醇受体循环利用。储存为膜结合视黄酯的视黄醇的动员由一种膜相关水解酶活性介导,该活性由作为释放的视黄醇载体的脱辅基CRBP水平选择性控制。在脱辅基CRBP(11 microM)存在下孵育时,高达90%的膜结合维生素A会释放出来,并伴随形成视黄醇-CRBP。整个过程中视黄醇无需离开其结合蛋白,这使得维生素A能够以膜结合视黄酯的形式积累,并作为视黄醇-CRBP复合物进行调节性动员。