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单糖转运至一种星虫动物——迪斯氏阔沙蚕血细胞的过程。

Monosaccharide transport into hemocytes of a sipunculan worm Themiste dyscrita.

作者信息

Ingermann R L, Hall R E, Bissonnette J M, Terwilliger R C

出版信息

Am J Physiol. 1985 Jul;249(1 Pt 2):R139-44. doi: 10.1152/ajpregu.1985.249.1.R139.

Abstract

The hemerythrin-containing blood cells, or hemocytes, of the sipunculan worm Themiste dyscrita were found to have a stereospecific and nonconcentrative monosaccharide transport system. The transport system transferred both D-glucose and 3-O-methyl-D-glucose (3-OMG), and transport into cells by this system was rapid, reaching 50% equilibrium in approximately 20 s at 10 degrees C with an initial concentration gradient of 0.1 mM; the contribution to total uptake by simple diffusion was very small. 3-OMG uptake showed saturation kinetics with a low half-saturation constant (Km less than or equal to 0.1 mM). The uptake of labeled 3-OMG by the hemocytes was strongly inhibited by unlabeled 3-OMG, 2-deoxy-D-glucose, alpha- and beta-D-glucose, D-galactose, and D-mannose. It was moderately inhibited by D-xylose, only slightly by alpha-methyl-D-glucoside and D-fructose, and uninhibited by sucrose, L-glucose, or D-sorbitol. Phloretin was more potent than phloridzin in blocking entry of 3-OMG. Cytochalasin B did not bind tightly to the T. dyscrita transporter and was not a potent inhibitor of transport; it half-maximally inhibited 3-OMG transport at 0.1 mM. Therefore, despite some differences the data suggest functional similarities in the mechanism of monosaccharide transport into blood cells of mammals and this invertebrate.

摘要

人们发现,星虫动物门的奇异索沙蚕(Themiste dyscrita)含血赤蛋白的血细胞(即血淋巴细胞)具有立体特异性且非浓缩性的单糖转运系统。该转运系统可转运D - 葡萄糖和3 - O - 甲基 - D - 葡萄糖(3 - OMG),通过此系统向细胞内的转运速度很快,在10℃下,初始浓度梯度为0.1 mM时,约20秒内即可达到50%的平衡;简单扩散对总摄取量的贡献非常小。3 - OMG的摄取呈现出饱和动力学,其半饱和常数较低(Km≤0.1 mM)。血细胞对标记的3 - OMG的摄取受到未标记的3 - OMG、2 - 脱氧 - D - 葡萄糖、α - 和β - D - 葡萄糖、D - 半乳糖以及D - 甘露糖的强烈抑制。它受到D - 木糖的中度抑制,受到α - 甲基 - D - 葡萄糖苷和D - 果糖的轻度抑制,而不受蔗糖、L - 葡萄糖或D - 山梨醇的抑制。根皮素在阻断3 - OMG进入方面比根皮苷更有效。细胞松弛素B与奇异索沙蚕转运体的结合不紧密,不是有效的转运抑制剂;在0.1 mM时,它对3 - OMG转运的抑制作用达到半数最大效应。因此,尽管存在一些差异,但这些数据表明哺乳动物和这种无脊椎动物的血细胞中单糖转运机制在功能上具有相似性。

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