BAC-mediated transgenic expression of fluorescent autophagic protein Beclin 1 reveals a role for Beclin 1 in lymphocyte development

被引:42
作者
Arsov, I. [1 ,2 ]
Li, X. [2 ]
Matthews, G. [1 ]
Coradin, J. [1 ]
Hartmann, B. [2 ]
Simon, A. K. [2 ,3 ]
Sealfon, S. C. [2 ]
Yue, Z. [2 ]
机构
[1] CUNY York Coll, Dept Biol, Jamaica, NY 11451 USA
[2] Mt Sinai Sch Med, Dept Neurol & Neurosci, New York, NY USA
[3] John Radcliffe Hosp, Nuffield Dept Clin Med, Weatherall Inst Mol Med, Oxford OX3 9DU, England
基金
美国国家卫生研究院;
关键词
beclin; 1; autophagy; T cell; B cell; apoptosis;
D O I
10.1038/cdd.2008.59
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
Beclin 1/Atg6 is an essential component of the evolutionary conserved PtdIns(3)-kinase (Vps34) protein complex that regulates macroautophagy (autophagy) in eukaryotic cells and also interacts with antiapoptotic Bcl-2 family members, Bcl-2, and Bcl-x(L). To elucidate the physiological function of Beclin 1, we generated transgenic mice producing a green fluorescent Beclin 1 protein (Beclin 1-GFP) under Beclin 1 endogenous regulation. The beclin 1-GFP transgene is functional because it completely rescues early embryonic lethality in beclin 1-deficient mice. The transgenic mice appear normal, with undetected change in basal autophagy levels in different tissues, despite the additional expression of functional Beclin 1-GFP. Staining of Beclin 1-GFP shows mostly diffuse cytoplasmic distribution in various tissues. Detailed analysis of the transgene expression by flow cytometry reveals a Bcl-2-like biphasic expression pattern in developing T and B cells, as well as differential regulation of expression in mature versus immature thymocytes following in vitro stimulation. Moreover, thymocytes expressing high Beclin 1-GFP levels appear increasingly sensitive to glucocorticoid-induced apoptosis in vitro. Our results, therefore, support a role for Beclin 1 in lymphocyte development involving cross talk between autophagy and apoptosis.
引用
收藏
页码:1385 / 1395
页数:11
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