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首页> 外文期刊>Pediatric Research >Purine and Phosphoribosylpyrophosphate Metabolism of Lymphocytes and Erythrocytes of an Adenosine Deaminase Deficient Immunocompetent Child
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Purine and Phosphoribosylpyrophosphate Metabolism of Lymphocytes and Erythrocytes of an Adenosine Deaminase Deficient Immunocompetent Child

机译:嘌呤和磷酸核糖焦磷酸酯代谢的腺苷脱氨酶缺乏症的儿童的淋巴细胞和红细胞。

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Summary: Purine metabolism and phosphoribosylpyrophosphate content of lymphocytes and erythrocytes were studied in an immunocompetent black male child with a total deficiency of erythrocyte and partial deficiency of lymphocyte adenosine deaminase. The partial genetic deficiency of adenosine deaminase was demonstrated in intact lymphocytes, and was approximately one third of the deaminating activity of control lymphocytes. Intact lymphocytes of the patient did not incorporate adenosine at a faster rate than those of control lymphocytes. The patient's erythrocytes deaminating activity was low and adenine ribonucleotide synthesis from adenosine was increased several fold, while adenine incorporation into purine ribonucleotides was comparable to that of control erythrocytes. Transfusion with packed erythrocytes temporarily improved the deaminating capacity of circulating erythrocytes, but did not reduce the elevated incorporation of adenosine into purine ribonucleotides.Phosphoribosylpyrophosphate content of the patient's lymphocytes and erythrocytes was not diminished. Incubation of erythrocytes with adenosine lowered phosphoribosylpyrophosphate content while incubation with phosphate increased phosphoribosylpyrophosphate content to the same extent in mutant and control erythrocytes.Speculation: The finding that the patient's lymphocytes can deaminate adenosine to some extent may explain why the rate of adenosine incorporation into purine ribonucleotides of his lymphocytes is not increased and immune function is not impaired. Deficiency of erythrocyte adenosine deaminase results in increased adenosine incorporation, but does not appear to interfere with immune functions.
机译:摘要:在一个具有免疫能力的黑人男孩中,研究了嘌呤的代谢以及淋巴细胞和红细胞的磷酸核糖焦磷酸含量,该患者完全缺乏红细胞,并且部分缺乏淋巴细胞腺苷脱氨酶。在完整的淋巴细胞中证实了腺苷脱氨酶的部分遗传缺陷,大约是对照淋巴细胞的脱氨活性的三分之一。患者的完整淋巴细胞没有以比对照淋巴细胞更快的速率掺入腺苷。患者的红细胞脱氨活性低,由腺苷合成的腺嘌呤核糖核苷酸增加了数倍,而将嘌呤掺入嘌呤核糖核苷酸的情况与对照红细胞相当。装满红细胞的输血暂时改善了循环红细胞的脱氨能力,但并未减少腺嘌呤掺入嘌呤核糖核苷酸的升高。患者淋巴细胞和红细胞的磷酸核糖焦磷酸含量并未降低。在突变体和对照性红细胞中,用腺苷孵育红细胞会降低磷酸核糖焦磷酸含量,而与磷酸盐孵育会增加磷酸核糖焦磷酸含量。淋巴细胞的数量没有增加,免疫功能也没有受损。红细胞腺苷脱氨酶的缺乏会导致腺苷掺入增加,但似乎不会干扰免疫功能。

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