Kumagai J, Johnson L R
Department of Physiology and Cell Biology, University of Texas Medical School, Houston 77030.
Am J Physiol. 1988 Jan;254(1 Pt 1):G81-6. doi: 10.1152/ajpgi.1988.254.1.G81.
Polyamines are necessary for the growth of eukaryotic cells and are supplied either by new synthesis or cellular uptake. To our knowledge, no information is available on polyamine uptake by gastrointestinal cells. In the current study, isolated villous enterocytes from the rat accumulated putrescine to an eightfold concentration gradient. Uptake was temperature dependent, saturable, and inhibited by 1 mM KCN. Kinetic analysis showed a Km of 1.23 X 10(-5) M and a Vmax of 2.60 X 10(-10) mol.10(6) cells-1.15 min-1. Enterocytes from the distal one-fourth of the gut showed the highest rate of uptake. Putrescine uptake was inhibited by cadaverine and spermine but not by the amino acids asparagine, AIB, or leucine. Sodium replacement by choline, lithium, N-methyl-D-glucamine, or tetramethylammonium significantly inhibited uptake, but replacement of Na+ by sucrose or mannitol was without effect. The inhibition observed was believed to be due to the ability of the cations to interact in some way with the carrier. Neither ouabain nor digitoxigenin had any effect on uptake. These data indicate that putrescine is accumulated by villous enterocytes by a carrier-mediated process that does not appear to involve Na+ contransport.
多胺是真核细胞生长所必需的,可通过新合成或细胞摄取来提供。据我们所知,尚无关于胃肠道细胞摄取多胺的相关信息。在本研究中,从大鼠分离出的绒毛状肠上皮细胞将腐胺积累至八倍浓度梯度。摄取过程依赖温度、具有饱和性,并受到1 mM KCN的抑制。动力学分析显示,其Km为1.23×10⁻⁵ M,Vmax为2.60×10⁻¹⁰ mol·10⁶细胞⁻¹·15 min⁻¹。来自肠道远端四分之一部位的肠上皮细胞摄取速率最高。腐胺的摄取受到尸胺和精胺的抑制,但不受天冬酰胺、AIB或亮氨酸等氨基酸的抑制。用胆碱、锂、N-甲基-D-葡糖胺或四甲基铵替代钠可显著抑制摄取,但用蔗糖或甘露醇替代Na⁺则无影响。据信所观察到的抑制是由于阳离子能够以某种方式与载体相互作用。哇巴因和洋地黄毒苷对摄取均无任何影响。这些数据表明,腐胺是通过绒毛状肠上皮细胞通过一种不涉及Na⁺共转运的载体介导过程而积累的。