Absence of mitochondrial uncoupling protein 1 affects apoptosis in thymocytes, thymocyte/T-cell profile and peripheral T-cell number

被引:17
作者
Adams, Alison E. [1 ]
Kelly, Orlagh M. [1 ]
Porter, Richard K. [1 ]
机构
[1] Trinity Coll Dublin, Sch Biochem & Immunol, Dublin 2, Ireland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2010年 / 1797卷 / 6-7期
基金
爱尔兰科学基金会;
关键词
Mitochondria; Uncoupling protein; Thymus; Spleen; UCP1-DEFICIENT MICE; SKELETAL-MUSCLE; PROTON LEAK; EXPRESSION; THYMUS; ACCLIMATION; FAMILY; SPLEEN;
D O I
10.1016/j.bbabio.2010.04.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Our laboratory has previously demonstrated the presence of constitutively expressed mitochondrial uncoupling protein 1 in mouse thymocytes. In our endeavours to understand the role of mitochondrial uncoupling protein 1 in thymocyte function, we compared cell profiles in thymus and spleen of wild-type with those of UCP 1 knock-out mice, which in turn led to comparative investigations of apoptotic potential in thymocytes from these mice. We demonstrate that spleen cell numbers were reduced similar to 3-fold in UCP 1 knock-out mice compared to wild-type mice. We record a halving of CD8 single positive cell numbers in thymus with a significant incremental increase in CD4/CD8 double positives cell numbers in the thymus of UCP 1 knock-out mice compared to wild-type mice. These data are mirrored by an approximate halving of CD8 single positive cell numbers and a doubling of CD4/CD8 double positive cell numbers in the spleen of UCP 1 knock-out mice compared to wild-type mice. These differences are most probably explained by our observations of decreased apoptotic potential and higher ATP levels in thymocytes of UCP 1 knock-out mice when compared to wild-type controls. We conclude that constitutively expressed UCP 1 is a factor in determining T-cell population selection in mice. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:807 / 816
页数:10
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