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视杆和视锥光感受器细胞外段中的糖酵解酶和一种GLUT-1葡萄糖转运蛋白。

Glycolytic enzymes and a GLUT-1 glucose transporter in the outer segments of rod and cone photoreceptor cells.

作者信息

Hsu S C, Molday R S

机构信息

Department of Biochemistry, Faculty of Medicine, University of British Columbia, Vancouver, Canada.

出版信息

J Biol Chem. 1991 Nov 15;266(32):21745-52.

PMID:1939198
Abstract

The presence of glycolytic enzymes and a GLUT-1-type glucose transporter in rod and cone outer segments was determined by enzyme activity assays, glucose uptake measurements, Western blotting, and immunofluorescence microscopy. Enzyme activities of six glycolytic enzymes including hexokinase, phosphofructokinase, aldolase, glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, pyruvate kinase, and lactate dehydrogenase, were found to be present in purified rod outer segment (ROS) preparations. Immunofluorescence microscopy of bovine and chicken retina sections labeled with monoclonal antibodies against glyceraldehyde-3-phosphate dehydrogenase, phosphoglycerate kinase, and lactate dehydrogenase have confirmed that these enzymes are present in rod and cone outer segments and not simply contaminants from the inner segments or other cells. Rod outer segments were also found to contain glucose transport activity as detected by 3-O-[14C]methylglucose uptake and exchange. The glucose transporter had a Km of 6.3 mM and a Vmax of 0.15 nmol of 3-O-methylglucose/s/mg of ROS membrane protein for net uptake and a Km of 29 mM and a Vmax of 1.06 nmol of 3-O-methylglucose/s/mg of ROS membrane protein for equilibrium exchange. These Km values for net uptake and equilibrium exchange are similar to values obtained for human red blood cells and are characteristic of GLUT-1-type glucose transporter. The transport was inhibited by both cytochalasin B and phloretin. Western blot analysis and immunofluorescence microscopy using type-specific glucose transporter antibodies indicated that both rod and cone outer segment plasma membranes have a GLUT-1 glucose transporter of Mr 45K as found in red blood cells and brain microsomal membranes. Solid-phase radioimmune competitive inhibition studies indicated that rod outer segment plasma membranes contained 15% the number of glucose transporters found in human red blood cell membranes and had an estimated density of 400 glucose transporter per micron2 of plasma membrane. These studies support the view that outer segments can generate energy in the form of ATP and GTP by anaerobic glycolysis to supply at least some of the energy requirements for phototransduction and other metabolic processes.

摘要

通过酶活性测定、葡萄糖摄取测量、蛋白质印迹法和免疫荧光显微镜法,确定了视杆和视锥细胞外段中糖酵解酶和GLUT-1型葡萄糖转运蛋白的存在。在纯化的视杆细胞外段(ROS)制剂中发现了包括己糖激酶、磷酸果糖激酶、醛缩酶、甘油醛-3-磷酸脱氢酶、磷酸甘油酸激酶、丙酮酸激酶和乳酸脱氢酶在内的六种糖酵解酶的酶活性。用抗甘油醛-3-磷酸脱氢酶、磷酸甘油酸激酶和乳酸脱氢酶的单克隆抗体标记的牛和鸡视网膜切片的免疫荧光显微镜检查证实,这些酶存在于视杆和视锥细胞外段,而不仅仅是来自内段或其他细胞的污染物。通过3-O-[14C]甲基葡萄糖摄取和交换检测发现,视杆细胞外段也含有葡萄糖转运活性。对于净摄取,葡萄糖转运蛋白的Km为6.3 mM,Vmax为0.15 nmol的3-O-甲基葡萄糖/秒/毫克ROS膜蛋白;对于平衡交换,Km为29 mM,Vmax为1.06 nmol的3-O-甲基葡萄糖/秒/毫克ROS膜蛋白。这些净摄取和平衡交换的Km值与人类红细胞获得的值相似,是GLUT-1型葡萄糖转运蛋白的特征。运输受到细胞松弛素B和根皮素的抑制。使用类型特异性葡萄糖转运蛋白抗体的蛋白质印迹分析和免疫荧光显微镜检查表明,视杆和视锥细胞外段质膜都有一个45K的GLUT-1葡萄糖转运蛋白,如在红细胞和脑微粒体膜中发现的那样。固相放射免疫竞争性抑制研究表明,视杆细胞外段质膜中葡萄糖转运蛋白的数量是人类红细胞膜中发现数量的15%,估计质膜密度为每平方微米400个葡萄糖转运蛋白。这些研究支持了这样一种观点,即外段可以通过无氧糖酵解以ATP和GTP的形式产生能量,以满足光转导和其他代谢过程的至少一些能量需求。

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