Ingenbleek Y, Young V
Department of Food Sciences, University Louis-Pasteur, Illkirch, Strasbourg, France.
Annu Rev Nutr. 1994;14:495-533. doi: 10.1146/annurev.nu.14.070194.002431.
The name "transthyretin" reflects the dual physiological roles of this tetrameric unglycosylated plasma protein. TTR is one of three specific carrier proteins involved in the transport of both thyroid hormones and of retinol through the mediation of RBP. TTR is a product of the visceral compartment, and its hepatic synthesis is exquisititely sensitive to both the adequacy and levels of protein and energy intakes--hence the proposal of TTR as a nutritional marker. To date, 38 TTR variants have been described, most of which are associated with variable degrees of cardiac and/or neural tissue amyloid deposits. All known variants arise from a single AA substitution due to single point mutation in the coding region of the TTR gene. Under acute stress conditions, the synthesis of TTR, RBP, and CBG is abruptly depressed by a cytokine-directed orchestration of new metabolic priorities, with a redistribution of organ and tissue protein pools. It is proposed that TTR, RBP, and CBG behave as acute-booster reactants (ABRs), actively participating in the cascade of metabolic events characterizing the stress reaction along pathways best explained by the free hormone/vitamin hypothesis. The latter is governed by the law of mass action--the spontaneous dissociation and instant uptake by hepatocytes of the ligands freed from their specific carrier proteins, which creates a transient hyperthyroid, hyperretinoid, and hypercortisolic climate. This response generally does not exceed four or five days because the initial impact of injury normally subsides, but it may last longer if complications occur. The magnitude and adequacy of the stress responses depend on the preceding nutritional status as assessed by TTR plasma levels and are proportionate to the severity of insult. Clinical, animal, and molecular studies concur to demonstrate the dualistic stimulatory or inhibitory effects triggered by the ligands, whose unmetabolized fractions are excreted in the urinary output. Thyroid hormones and retinoids appear to control the early maturation processes and the synthesis of primary transcripts, whereas cortisol preferentially modulates the secondary responses and confers a protective effect on healthy tissues. During acute stress, the evolutionary patterns of visceral proteins and inflammatory markers exhibit compulsory mirror images. However, they change in independent ways under more chronic circumstances. A relatively simple biochemical micromethod based on the simultaneous measurement of plasma TTR, albumin, CRP, and orosomucoid aggregated into a PINI is proposed for the early recognition and follow-up of both nutritional and inflammatory facets of the disease spectrum.
“转甲状腺素蛋白”这个名称反映了这种四聚体无糖基化血浆蛋白的双重生理作用。转甲状腺素蛋白是三种特定载体蛋白之一,通过视黄醇结合蛋白(RBP)的介导参与甲状腺激素和视黄醇的运输。转甲状腺素蛋白是内脏腔室的产物,其肝脏合成对蛋白质和能量摄入的充足程度和水平极为敏感,因此有人提议将转甲状腺素蛋白作为一种营养标志物。迄今为止,已描述了38种转甲状腺素蛋白变体,其中大多数与不同程度的心脏和/或神经组织淀粉样沉积物有关。所有已知变体均由转甲状腺素蛋白基因编码区的单点突变导致的单个氨基酸取代引起。在急性应激条件下,转甲状腺素蛋白、视黄醇结合蛋白和皮质类固醇结合球蛋白的合成会因细胞因子引导的新代谢优先级编排而突然受到抑制,同时器官和组织蛋白池会重新分布。有人提出,转甲状腺素蛋白、视黄醇结合蛋白和皮质类固醇结合球蛋白表现为急性增强反应物(ABR),通过游离激素/维生素假说能最好解释的途径,积极参与表征应激反应的代谢事件级联。后者受质量作用定律支配——配体从其特定载体蛋白上自发解离并被肝细胞立即摄取,这会营造一种短暂的甲状腺功能亢进、视黄醇过多和皮质醇过多的状态。这种反应通常不会超过四五天,因为损伤的初始影响通常会消退,但如果出现并发症,可能会持续更长时间。应激反应的强度和充分程度取决于通过血浆转甲状腺素蛋白水平评估的先前营养状况,并与损伤的严重程度成正比。临床、动物和分子研究一致证明配体引发的二元刺激或抑制作用,其未代谢部分会随尿液排出。甲状腺激素和类视黄醇似乎控制早期成熟过程和初级转录本的合成,而皮质醇则优先调节次级反应并对健康组织产生保护作用。在急性应激期间,内脏蛋白和炎症标志物的进化模式呈现出强制的镜像关系。然而,在更慢性的情况下,它们会以独立的方式发生变化。有人提出一种相对简单的生化微量方法,基于同时测量血浆转甲状腺素蛋白、白蛋白、C反应蛋白和结合珠蛋白聚合成一个PINI,用于疾病谱营养和炎症方面的早期识别和随访。