Rossard Stéphanie, Bonmort Janine, Guinet Frédéric, Ponchet Michel, Roblin Gabriel
Laboratoire de Physiologie, Biochimie et Biologie Moléculaire Végétales, University of Poitiers, UMR CNRS 6161, 40 avenue du Recteur Pineau, 86022 Poitiers, France.
Planta. 2003 Dec;218(2):288-99. doi: 10.1007/s00425-003-1094-4. Epub 2003 Aug 15.
The uptake of cholesterol has been characterized in leaf discs from mature leaves of sugar beet ( Beta vulgaris L.). This transport system exhibited a simple saturable phase with an apparent Michaelis constant ranging from 30 to 190 microM depending on the sample. When present at 10 M excess, other sterols were able to inhibit cholesterol uptake. Moreover, binding assays demonstrated the presence of high-affinity binding sites for cholesterol in purified plasma membrane vesicles. In the range 1-60 microM, cholesterol uptake showed an active component evidenced by action of the protonophore carbonyl cyanide m-chlorophenylhydrazone. Energy was required as shown by the inhibition of uptake induced by respiration inhibitors (NaN(3)), darkness and photosynthesis inhibitors [3-(3,4-dichlorophenyl)-1,1-dimethylurea, methyl viologen]. Moreover, the process was strongly dependent on the experimental temperature. Uptake was optimal at acidic pH (4.0), sensitive to ATPase modulators, inhibited by thiol reagents (N-ethylmaleimide, p-chloromercuribenzenesulfonic acid, Mersalyl) and by the histidyl-group reagent diethyl pyrocarbonate. The addition of cholesterol did not modify H(+) flux from tissues, indicating that H(+)-co-transport was unlikely to be involved. MgATP did not increase the uptake, arguing against involvement of an ABC cassette-type transporter. By contrast, cryptogein, a sterol carrier protein from the Oomycete Phytophtora cryptogea, greatly increased absorption. Taken together, the results reported in this work suggest that plant cells contain a specific plasma membrane transport system for sterols.
已对甜菜(Beta vulgaris L.)成熟叶片的叶圆片摄取胆固醇的特性进行了研究。该转运系统表现出一个简单的饱和阶段,根据样品不同,其表观米氏常数范围为30至190微摩尔。当其他固醇以10倍过量存在时,能够抑制胆固醇摄取。此外,结合试验证明在纯化的质膜囊泡中存在胆固醇的高亲和力结合位点。在1至60微摩尔范围内,胆固醇摄取显示出一个活性成分,质子载体羰基氰化物间氯苯腙的作用证明了这一点。如呼吸抑制剂(NaN₃)、黑暗和光合作用抑制剂[3-(3,4-二氯苯基)-1,1-二甲基脲、甲基紫精]诱导的摄取抑制所示,摄取需要能量。此外,该过程强烈依赖于实验温度。摄取在酸性pH(4.0)下最佳,对ATP酶调节剂敏感,被硫醇试剂(N-乙基马来酰亚胺、对氯汞苯磺酸、汞撒利)和组氨酸基团试剂焦碳酸二乙酯抑制。胆固醇的添加并未改变组织中的H⁺通量,表明不太可能涉及H⁺共转运。MgATP并未增加摄取,这与ABC盒式转运蛋白的参与相悖。相比之下,隐地蛋白,一种来自卵菌纲植物疫霉的固醇载体蛋白,大大增加了吸收。综上所述,这项工作报道的结果表明植物细胞含有一种特定的质膜固醇转运系统。