Identification of soluble and membrane-bound isoforms of porcine tumor necrosis factor receptor 2

被引:6
|
作者
Uribe-Herranz, Mireia [1 ]
Casinghino, Sandra R. [2 ,3 ]
Bosch-Presegue, Laia [1 ]
Fodor, William L. [2 ,3 ]
Costa, Cristina [1 ,2 ]
机构
[1] Hosp Duran & Reynals, Inst Invest Biomed Bellvitge IDIBELL, New Therapies Genes & Transplants Grp, Barcelona 08908, Spain
[2] Alex Pharmaceut Inc, Dept Mol Sci, Cheshire, CT USA
[3] Univ Connecticut, Dept Mol & Cell Biol, CT Ctr Regenerat Biol, Storrs, CT 06269 USA
关键词
cytokine; endothelium; tumor necrosis factor; tumor necrosis factor R2; Xenotransplantation; DELAYED XENOGRAFT REJECTION; ENDOTHELIAL-CELLS; FACTOR TNF; T-CELLS; IN-VIVO; ACTIVATION; EXPRESSION; ALPHA; DEATH; XENOTRANSPLANTATION;
D O I
10.1111/j.1399-3089.2011.00634.x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: TNF and its receptors TNF-Receptor 1 (TNFR1, CD120a) and TNF-Receptor 2 (TNFR2, CD120b) have been implicated in the rejection of transplanted cells and organs. Although pig TNFR1 (pTNFR1) is known to mediate the effects of human TNF in a xenogeneic setting, it is unclear whether pig TNFR2 (pTNFR2) could contribute to xenograft rejection. Methods: We have cloned the cDNA of various pTNFR2 variants by reverse transcription-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends. We have characterized the predicted proteins with bioinformatic tools and conducted expression, affinity, and functional studies to investigate their roles. Results: We have identified four isoforms of pTNFR2: one comprising the four cysteine-rich domains (CRD) conserved between species, a shorter variant (pTNFR2 Delta E7-10) encoding for a soluble isoform, another with only three CRD due to the lack of exon 4 (pTNFR2 Delta E4), and a fourth variant containing both modifications. Accordingly, multiple mRNA transcripts were observed by northern blotting. Quantitative RT-PCR determined high pTNFR2 expression in lung and immune cells and detected the two alternative splicings in all cells/tissues examined. The full receptor was moderately expressed on the surface of pig cells such as porcine aortic endothelial cells and PK-15 and was regulated by TNF. On the contrary, the membrane-bound pTNFR2 Delta E4 was located only intracellularly. Plasmon resonance studies showed that pTNFR2 binds pig and human TNF alpha with high affinity, but pTNFR2 Delta E4 interacts poorly with pig TNF alpha and does not bind to the human cytokine. Moreover, pull-down experiments with the two recombinant soluble isoforms consistently demonstrated that the two bound together and soluble pTNFR2 Delta E4 was able to modulate the TNF inhibitory activity of pTNFR2-GST in a cell-based assay. Conclusion: The pTNFR2 may participate in the process of xenograft rejection and other related events, as well as be used in soluble form to block TNF in this setting. In addition, we have discovered other pTNFR2 isoforms that may affect the pig immune responses and have an impact on rejection of xenografts.
引用
收藏
页码:131 / 146
页数:16
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