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N-Glycolylneuraminic Acid (Neu5Gc) Null Large Animals by Targeting the CMP-Neu5Gc Hydroxylase (CMAH)

机译:通过针对CMP-Neu5Gc羟化酶(CMAH)的N-乙二醇神经氨酸(Neu5Gc)的大型动物

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摘要

The two major sialic acids described in mammalian cells are the N-glycolylneuraminic acid (Neu5Gc) and the N-acetylneuraminic acid (Neu5Ac). Neu5Gc synthesis starts from the N-acetylneuraminic acid (Neu5Ac) precursor modified by an hydroxylic group addition catalyzed by CMP-Neu5Ac hydroxylase enzyme (CMAH). In humans, CMAH was inactivated by a 92 bp deletion occurred 2–3 million years ago. Few other mammals do not synthetize Neu5Gc, however livestock species used for food production and as a source of biological materials for medical applications carry Neu5Gc. Trace amounts of Neu5Gc are up taken through the diet and incorporated into various tissues including epithelia and endothelia cells. Humans carry “natural,” diet-induced Anti-Neu5Gc antibodies and when undertaking medical treatments or receiving transplants or devices that contain animal derived products they can cause immunological reaction affecting pharmacology, immune tolerance, and severe side effect like serum sickness disease (SSD). Neu5Gc null mice have been the main experimental model to study such phenotype. With the recent advances in genome editing, pigs and cattle KO for Neu5Gc have been generated always in association with the αGal KO. These large animals are normal and fertile and provide additional experimental models to study such mutation. Moreover, they will be the base for the development of new therapeutic applications like polyclonal IgG immunotherapy, Bioprosthetic Heart Valves, cells and tissues replacement.
机译:哺乳动物细胞中描述的两种主要唾液酸是N-羟乙酰神经氨酸(Neu5Gc)和N-乙酰神经氨酸(Neu5Ac)。 Neu5Gc的合成始于被CMP-Neu5Ac羟化酶(CMAH)催化的羟基加成修饰的N-乙酰神经氨酸(Neu5Ac)前体。在人类中,CMAH因2到300万年前发生的92 bp缺失而失活。很少有其他哺乳动物不合成Neu5Gc,但是用于食品生产和医学用途的生物材料来源的牲畜物种携带Neu5Gc。通过饮食摄取微量的Neu5Gc,并掺入包括上皮和内皮细胞在内的各种组织中。人类携带“天然的”饮食诱导的抗Neu5Gc抗体,当进行医学治疗或接受包含动物衍生产品的移植物或设备时,它们会引起免疫反应,从而影响药理学,免疫耐受性以及严重的副作用,例如血清病(SSD) 。 Neu5Gc无效小鼠已成为研究此类表型的主要实验模型。随着基因组编辑的最新进展,Neu5Gc的猪和牛KO始终与αGalKO结合产生。这些大型动物正常且肥沃,并提供了额外的实验模型来研究此类突变。此外,它们将成为开发新的治疗应用程序的基础,例如多克隆IgG免疫疗法,生物假体心脏瓣膜,细胞和组织替代。

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