An endogenous hybrid mRNA encodes TWE-PRIL, a functional cell surface TWEAK-APRIL fusion protein

被引:116
作者
Pradet-Balade, B
Medema, JP
López-Fraga, M
Lozano, JC
Kolfschoten, GM
Picard, A
Martínez, C
Garcia-Sanz, JA [1 ]
Hahne, M
机构
[1] Ctr Nacl Biotecnol, Dept Immunol & Oncol, E-28049 Madrid, Spain
[2] Leiden Univ, Dept Immunohematol & Blood Transfus, Med Ctr, NL-2333 ZA Leiden, Netherlands
[3] Lab Arago, Observ Banyuls, UMR 7628,CNRS, Lab Arago, F-66650 Banyuls sur Mer, France
关键词
APRIL; cell membrane anchoring; hybrid mRNA; TNF family; TWEAK;
D O I
10.1093/emboj/cdf565
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
TWEAK and APRIL are two recently identified tumour necrosis factor (TNF) ligand family members, implicated in angiogenesis and immune regulation, respectively. TWEAK is a transmembrane protein expressed on the cell surface, whereas APRIL acts solely as a secreted factor. In this report, using RACE, RT-PCR, cDNA library screening and an RNase protection assay, we characterize a hybrid transcript between TWEAK and APRIL mRNAs. The encoded TWE-PRIL protein is composed of TWEAK cytoplasmic and transmembrane domains fused to the APRIL C-terminal domain. TWE-PRIL mRNA is expressed and translated in human primary T cells and monocytes, and endogenous TWE-PRIL protein was detected in primary human T lymphocytes and monocytic cell lines. TWE-PRIL is membrane anchored and presents the APRIL receptor-binding domain at the cell surface. It is a biologically active ligand, as it stimulates cycling in T- and B-lymphoma cell lines. Much like membrane-bound and secreted TNF-alpha, the different cellular localizations of TWE-PRIL and APRIL suggest that they exert distinct biological roles.
引用
收藏
页码:5711 / 5720
页数:10
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