Dumler F, Cortes P
Department of Medicine, Henry Ford Hospital, Detroit, Michigan 48202.
Am J Physiol. 1988 Dec;255(6 Pt 1):C712-8. doi: 10.1152/ajpcell.1988.255.6.C712.
Uridine diphosphosugars (UDP-sugars: UDP-N-acetylglucosamine, UDP-glucose, and UDP-glucuronic acid) are essential coenzymes for the synthesis of glomerular basement membrane and mesangial matrix (GBM-MM). This study has characterized UDP-sugar metabolism in rat and human glomerular cells in tissue culture. Culture of rat mesangial cells in medium containing dialyzed fetal calf serum resulted in UTP loss (28 +/- 4 nmol.mg DNA-1.h-1); the addition of 2 microM orotate to this medium resulted in net UTP accretion (5.42 +/- 0.06 nmol.mg DNA-1.h-1). Rat mesangial cells demonstrated 16- and 29- to 46-fold greater UTP and UDP-sugar pools, respectively, than whole glomeruli. In human mesangial cells, 6-azauridine (500 microM) decreased UDP-sugar pools by 48% (P less than 0.05), whereas uridine (50 microM) produced a 2.5-fold increase. Human and rat mesangial cells had greater (1.8- to 6.1-fold) UDP-sugar pools than epithelial cells and 1.7-3.4 times greater labeled precursor incorporation into UDP-sugars. In conclusion, glomerular cells utilize both exogenous orotate and uridine for ribonucleotide synthesis, and the extracellular concentration of these precursors markedly influence the formation and cellular content of UDP-sugars. Prominent differences exist between separate glomerular cell populations in their metabolism of UDP-sugars. This may represent diverse activity of glycosylating reactions.
尿苷二磷酸糖(UDP-糖:UDP-N-乙酰葡糖胺、UDP-葡萄糖和UDP-葡糖醛酸)是肾小球基底膜和系膜基质(GBM-MM)合成所必需的辅酶。本研究已对组织培养中大鼠和人肾小球细胞的UDP-糖代谢进行了表征。在含有透析胎牛血清的培养基中培养大鼠系膜细胞导致UTP损失(28±4 nmol·mg DNA⁻¹·h⁻¹);向该培养基中添加2 μM乳清酸导致UTP净增加(5.42±0.06 nmol·mg DNA⁻¹·h⁻¹)。大鼠系膜细胞的UTP池和UDP-糖池分别比整个肾小球大16倍和29至46倍。在人系膜细胞中,6-氮杂尿苷(500 μM)使UDP-糖池减少48%(P<0.05),而尿苷(50 μM)使UDP-糖池增加2.5倍。人和大鼠系膜细胞的UDP-糖池比上皮细胞大(1.8至6.1倍),且标记前体掺入UDP-糖的量是上皮细胞的1.7至3.4倍。总之,肾小球细胞利用外源性乳清酸和尿苷进行核糖核苷酸合成,这些前体的细胞外浓度显著影响UDP-糖的形成和细胞含量。不同肾小球细胞群体在UDP-糖代谢方面存在显著差异。这可能代表了糖基化反应的不同活性。