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Impaired T cell function in argininosuccinate synthetase deficiency
被引:37
作者:
Tarasenko, Tatyana N.
[1
]
Gomez-Rodriguez, Julio
[1
]
McGuire, Peter J.
[1
]
机构:
[1] NHGRI, NIH, Bethesda, MD 20892 USA
基金:
美国国家卫生研究院;
关键词:
immunity;
arginine;
metabolism;
differentiation;
L-ARGININE;
GENE-EXPRESSION;
ZETA-CHAIN;
AMINO-ACID;
METABOLISM;
PROLIFERATION;
LYMPHOCYTES;
CITRULLINE;
D O I:
10.1189/jlb.1AB0714-365R
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
ASS1 is a cytosolic enzyme that plays a role in the conversion of citrulline to arginine. In human and mouse tissues, ASS1 protein is found in several components of the immune system, including the thymus and T cells. However, the role of ASS1 in these tissues remains to be defined. Considerable attention has been focused recently on the role of metabolism in T cell differentiation and function. Based on the expression of ASS1 in the immune system, we hypothesized that ASS1 deficiency would result in T cell defects. To evaluate this question, we characterized immune function in hypomorphic fold/fold mice. Analysis of splenic T cells by flow cytometry showed a marked reduction in T cell numbers with normal expression of activation surface markers. Gene therapy correction of liver ASS1 to enhance survival resulted in a partial recovery of splenic T cells for characterization. In vitro and in vivo studies demonstrated the persistence of the ASS1 enzyme defect in T cells and abnormal T cell differentiation and function. Overall, our work suggests that ASS1 plays a role in T cell function, and deficiency produces primary immune dysfunction. In addition, these data suggest that patients with ASS1 deficiency (citrullinemia type I) may have T cell dysfunction.
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页码:273 / 278
页数:6
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