Mutational analysis of pig tissue factor pathway inhibitor α to increase anti-coagulation activity in pig-to-human xenotransplantation.

IF 2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Letters Pub Date : 2024-08-01 Epub Date: 2024-06-13 DOI:10.1007/s10529-024-03505-z
Chang-Hee Lee, Hyeon Jeong Lee, Si-Won Park, Jiyoon Shin, Seok-Jin Kang, In-Byung Park, Hyun Kyung Kim, Taehoon Chun
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Abstract

Blood coagulation mediated by pig tissue factor (TF), which is expressed in pig tissues, causes an instant blood-mediated inflammatory reaction during pig-to-human xenotransplantation. Previously, we generated a soluble pig tissue factor pathway inhibitor α fusion immunoglobulin (TFPI-Ig) which inhibits pig TF activity more efficiently than human TFPI-Ig in human plasma. In this study, we generated several pig TFPI-Ig mutants and tested the efficacy of these mutants in preventing pig-to-human xenogeneic blood coagulation. Structurally important amino acid residues of pig TFPI-Ig were changed into different residues by site-directed mutagenesis. Subsequently, a retroviral vector encoding each cDNA of several pig TFPI-Ig mutants was cloned and transduced into CHO-K1 cells. After establishing stable cell lines expressing each of the pig TFPI-Ig mutants, soluble proteins were produced and purified for evaluating their inhibitory effects on pig TF-mediated blood coagulation in human plasma. The replacement of K36 and K257 with R36 and H257, respectively, in pig TFPI-Ig more efficiently blocked pig TF activity in human plasma when compared with the wild-type pig TFPI-Ig. These results may provide additional information to understand the structure of pig TFPIα, and an improved pig TFPI-Ig variant that more efficiently blocks pig TF-mediated blood coagulation during pig-to-human xenotransplantation.

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对猪组织因子通路抑制剂α进行突变分析,以提高猪-人异种移植中的抗凝血活性。
猪组织中表达的猪组织因子(TF)介导的血液凝固会在猪对人异种移植过程中引起瞬间的血液介导的炎症反应。此前,我们生成了一种可溶性猪组织因子通路抑制剂α融合免疫球蛋白(TFPI-Ig),与人血浆中的人TFPI-Ig相比,它能更有效地抑制猪TF的活性。在这项研究中,我们生成了几种猪 TFPI-Ig 突变体,并测试了这些突变体在防止猪对人异种血液凝固方面的功效。通过定点突变将猪 TFPI-Ig 结构上重要的氨基酸残基改变为不同的残基。随后,克隆了编码几种猪 TFPI-Ig 突变体 cDNA 的逆转录病毒载体,并将其转导到 CHO-K1 细胞中。在建立了表达每种猪 TFPI-Ig 突变体的稳定细胞系后,生产并纯化了可溶性蛋白,以评估它们对猪 TF 介导的人血浆血液凝固的抑制作用。与野生型猪 TFPI-Ig 相比,用 R36 和 H257 分别取代猪 TFPI-Ig 中的 K36 和 K257 能更有效地阻断人血浆中猪 TF 的活性。这些结果可为了解猪 TFPIα 的结构提供更多信息,并可提供一种改进的猪 TFPI-Ig 变体,在猪对人异种移植过程中更有效地阻断猪 TF 介导的血液凝固。
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来源期刊
Biotechnology Letters
Biotechnology Letters 工程技术-生物工程与应用微生物
CiteScore
5.90
自引率
3.70%
发文量
108
审稿时长
1.2 months
期刊介绍: Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them. All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included. Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields. The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories. Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.
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