German Red Cross Blood Service West, Bad Kreuznach and Hagen, Germany; Center for Innovation Competence: Humoral Immune Reactions in Cardiovascular Diseases (ZIK HIKE); Institute of Immunology and Transfusion Medicine, University Hospital Greifswald, Greifswald, Germany; Clinical and Experimental Pathology, Research Center Borstel, Airway Research Center North, Member of the German Center for Lung Research, Borstel, Germany.
Transfusion. 2013 Dec;53(12):3217-23. doi: 10.1111/trf.12160. Epub 2013 Mar 11.
The HNA-3a antigen is an important antibody target in the pathophysiology of transfusion-related acute lung injury (TRALI). It is encoded by the choline transporter-like protein 2 (CTL2) gene, which exists in the two transcript variants TV1 and TV2, differing in the upstream promoter and coding region. Only TV1 has been demonstrated to enable choline transport across the cell membrane.
The aim of this study was to determine the CTL2 transcript pattern in human peripheral blood cells and tissues and its capacity to bind HNA-3a antibodies. RNA was isolated from human whole blood, isolated neutrophils, mononuclear blood cells, leukoreduced platelets, human lung, liver, and colon. After reverse transcription, the single-stranded cDNA was amplified using primer combinations specific for the respective transcript. Plasmids containing the entire CTL2 coding cDNA of the transcript variant TV1 or TV2 served as controls. HEK293T cells expressing both variants were used to determine the binding of HNA-3a antibodies.
The shorter TV2 transcript was demonstrated in each RNA sample derived from human peripheral blood tested so far, as well as in human lung and liver, whereas the longer TV1 transcript was only detected in human lung and colon. TV1 and TV2 had the same binding capacity to HNA-3a antibodies.
The expression of TV1 and TV2 is tissue and cell specific, with peripheral blood cells expressing only TV2. This does not affect binding of HNA-3a antibodies. Whether the unequal expression might be relevant in the pathogenesis of TRALI remains to be investigated.
HNA-3a 抗原是输血相关性急性肺损伤(TRALI)病理生理学中的一个重要抗体靶标。它由胆碱转运蛋白样蛋白 2(CTL2)基因编码,该基因存在两个转录变体 TV1 和 TV2,在启动子上游和编码区存在差异。只有 TV1 已被证明能够使胆碱跨细胞膜转运。
本研究旨在确定 CTL2 转录本在人外周血细胞和组织中的模式及其与 HNA-3a 抗体结合的能力。从人全血、分离的嗜中性粒细胞、单核细胞、白细胞减少的血小板、人肺、肝和结肠中分离 RNA。逆转录后,使用针对各自转录本的引物组合扩增单链 cDNA。包含转录变体 TV1 或 TV2 的全长 CTL2 编码 cDNA 的质粒用作对照。表达两种变体的 HEK293T 细胞用于确定 HNA-3a 抗体的结合。
迄今为止,在测试的每种源自人外周血的 RNA 样本中都证明了较短的 TV2 转录本的存在,以及在人肺和肝中,而较长的 TV1 转录本仅在人肺和结肠中检测到。TV1 和 TV2 对 HNA-3a 抗体具有相同的结合能力。
TV1 和 TV2 的表达具有组织和细胞特异性,外周血细胞仅表达 TV2。这并不影响 HNA-3a 抗体的结合。在 TRALI 的发病机制中,这种不均匀的表达是否相关仍有待研究。