Pajor A M, Moon D A, Wright S H
Department of Physiology, College of Medicine, University of Arizona, Tucson 85724.
J Membr Biol. 1989 Jan;107(1):77-88. doi: 10.1007/BF01871085.
Glucose transport was studied in marine mussels of the genus Mytilus. Initial observations, with intact animals and isolated gills, indicated that net uptake of glucose occurred in mussels by a carrier-mediated, Na+-sensitive process. Subsequent studies included use of brush-border membrane vesicles (BBMV) in order to characterize this transport in greater detail. The highest activity of Na+-dependent glucose transport was found in the brush-border membrane fractions used in this study, while basal-lateral membrane fractions contained the highest specific binding of ouabain. Glucose uptake into BBMV showed specificity for Na+, and concentrative glucose transport was observed in the presence of an inwardly directed Na+ gradient. There was a single saturable pathway for glucose uptake, with an apparent Kt of 3 microM in BBMV and 9 microM in intact gills. The kinetics of Na+ activation of glucose uptake were sigmoidal, with apparent Hill coefficients of 1.5 in BBMV and 1.2 in isolated gills, indicating that more than one Na+ may be involved in the transport of each glucose. Harmaline inhibited glucose transport in mussel BBMV with a Ki of 44 microM. The uptake of glucose was electrogenic and stimulated by an inside-negative membrane potential. The substrate specificity in intact gills and BBMV resembled that of Na+-glucose cotransporters in other systems; D-glucose and alpha-methyl glucopyranoside were the most effective inhibitors of Na+-glucose transport, D-galactose was intermediate in its inhibition, and there was little or no effect of L-glucose, D-fructose, 2-deoxy-glucose, or 3-O-methyl glucose. Phlorizin was an effective inhibitor of Na+-glucose uptake, with an apparent Ki of 154 nM in BBMV and 21 nM in intact gills. While the qualitative characteristics of glucose transport in the mussel gill were similar to those in other epithelia, the quantitative characteristics of this process reflect adaptation to the seawater environment of this animal.
对贻贝属的海洋贻贝的葡萄糖转运进行了研究。对完整动物和分离鳃的初步观察表明,贻贝中葡萄糖的净摄取是通过载体介导的、对Na⁺敏感的过程发生的。随后的研究包括使用刷状缘膜囊泡(BBMV),以便更详细地描述这种转运。在本研究中使用的刷状缘膜组分中发现了最高活性的Na⁺依赖性葡萄糖转运,而基底外侧膜组分含有最高特异性的哇巴因结合。葡萄糖摄取到BBMV中显示出对Na⁺的特异性,并且在存在内向Na⁺梯度的情况下观察到浓缩性葡萄糖转运。葡萄糖摄取有一条单一的可饱和途径,在BBMV中表观Kt为3 microM,在完整鳃中为9 microM。葡萄糖摄取的Na⁺激活动力学呈S形,在BBMV中表观希尔系数为1.5,在分离鳃中为1.2,表明每个葡萄糖的转运可能涉及不止一个Na⁺。哈尔明碱抑制贻贝BBMV中的葡萄糖转运,Ki为44 microM。葡萄糖摄取是生电的,并受到内膜负电位的刺激。完整鳃和BBMV中的底物特异性类似于其他系统中Na⁺ - 葡萄糖共转运体的底物特异性;D - 葡萄糖和α - 甲基吡喃葡萄糖苷是Na⁺ - 葡萄糖转运的最有效抑制剂,D - 半乳糖的抑制作用中等,而L - 葡萄糖、D - 果糖、2 - 脱氧 - 葡萄糖或3 - O - 甲基葡萄糖几乎没有影响。根皮苷是Na⁺ - 葡萄糖摄取的有效抑制剂,在BBMV中表观Ki为154 nM,在完整鳃中为21 nM。虽然贻贝鳃中葡萄糖转运的定性特征与其他上皮细胞中的相似,但该过程的定量特征反映了该动物对海水环境的适应性。