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患有小叶间胆管稀少综合征(阿拉吉列综合征)儿童的成纤维细胞培养物中的2-脱氧-D-葡萄糖摄取及脂肪酸含量

2-Deoxy-D-glucose uptake and fatty acid content in fibroblast cultures from children with syndromic paucity of interlobular bile ducts (Alagille syndrome).

作者信息

Couturier M, Lemonnier F

机构信息

Unité de Recherche d' Hépatologie Pédiatrique INSERM U56, Hôpital Bicêtre, France.

出版信息

J Inherit Metab Dis. 1991;14(2):215-27. doi: 10.1007/BF01800593.

DOI:10.1007/BF01800593
PMID:1886406
Abstract

2-Deoxy-D-glucose (2-DOG) uptake was studied in skin fibroblast cultures from control children and children with Alagille syndrome or syndromic paucity of interlobular bile ducts (PILBD). No significant differences in uptake were observed between patients and controls. However, as the scatter of the results was larger in the fibroblasts from patients, we attempted to establish for these patients a relationship between 2-DOG uptake and some biochemical parameters. We observed an inverse relationship between this uptake and the levels of plasma cholesterol and phospholipids (r = -0.85). Compared to controls, 2-DOG uptake was significantly lower in cultures from patients who had very high levels of cholesterol (P2 group), but not in cultures from patients with moderately increased levels of cholesterol (P1 group). The level of total cellular cholesterol in cultured cells from the P1 and P2 groups was not significantly different from the control level, but we found marked differences between the concentrations of fatty acids. In the cultures from patients (especially the P2 group), we observed a significant increase in total fatty acids; among the saturated fatty acids, this increase chiefly concerned the 18:0 (14%) and among the polyunsaturated the n - 3 fatty acids (55%). The high concentrations of 20:5, 22:5 and 22:6, which enhance membrane fluidity, might explain the decrease in 2-DOG uptake found in the cultures from patients (P2 group) with PILBD. The nature of these abnormalities might be connected with the genetic origin of Alagille syndrome.

摘要

对来自对照儿童以及患有阿拉吉耶综合征或综合征性小叶间胆管缺乏症(PILBD)的儿童的皮肤成纤维细胞培养物中的2-脱氧-D-葡萄糖(2-DOG)摄取情况进行了研究。患者与对照之间在摄取方面未观察到显著差异。然而,由于患者的成纤维细胞结果的离散度更大,我们试图为这些患者建立2-DOG摄取与一些生化参数之间的关系。我们观察到这种摄取与血浆胆固醇和磷脂水平呈负相关(r = -0.85)。与对照相比,胆固醇水平非常高的患者(P2组)的培养物中2-DOG摄取显著更低,但胆固醇水平中度升高的患者(P1组)的培养物中并非如此。P1组和P2组培养细胞中的总细胞胆固醇水平与对照水平无显著差异,但我们发现脂肪酸浓度存在显著差异。在患者的培养物中(尤其是P2组),我们观察到总脂肪酸显著增加;在饱和脂肪酸中,这种增加主要涉及18:0(14%),在多不饱和脂肪酸中则涉及n - 3脂肪酸(55%)。可增强膜流动性的20:5、22:5和22:6的高浓度可能解释了PILBD患者(P2组)培养物中2-DOG摄取的降低。这些异常的性质可能与阿拉吉耶综合征的遗传起源有关。

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引用本文的文献

1
Fatty acid content in lymphocytes from children with syndromic paucity of interlobular bile ducts, Alagille syndrome.患有小叶间胆管综合征(阿拉吉耶综合征)的儿童淋巴细胞中的脂肪酸含量
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