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触珠蛋白相关蛋白是一种高亲和力结合血红蛋白的血浆蛋白。

Haptoglobin-related protein is a high-affinity hemoglobin-binding plasma protein.

作者信息

Nielsen Marianne Jensby, Petersen Steen Vang, Jacobsen Christian, Oxvig Claus, Rees David, Møller Holger Jon, Moestrup Søren Kragh

机构信息

Department of Medical Biochemistry, University of Aarhus, DK-8000 Aarhus C, Denmark.

出版信息

Blood. 2006 Oct 15;108(8):2846-9. doi: 10.1182/blood-2006-05-022327. Epub 2006 Jun 15.

Abstract

Haptoglobin-related protein (Hpr) is a primate-specific plasma protein associated with apolipoprotein L-I (apoL-I)-containing high-density lipoprotein (HDL) particles shown to be a part of the innate immune defense. Despite the assumption hitherto that Hpr does not bind to hemoglobin, the present study revealed that recombinant Hpr binds hemoglobin as efficiently as haptoglobin (Hp). However, in contrast to Hp, Hpr did not promote any high-affinity binding to the scavenger receptor CD163. Binding of hemoglobin to circulating native Hpr incorporated into the HDL fraction was indicated by hemoglobin-affinity precipitation of plasma Hpr together with apoL-I. In conclusion, plasma has 2 high-affinity hemoglobin-binding haptoglobins instead of one, but only Hp-hemoglobin complexes are efficiently recognized by CD163. Circulating Hpr-bound hemoglobin should therefore be taken into consideration when measuring "free" plasma hemoglobin. Furthermore, Hpr-bound hemoglobin might contribute to the biologic activity of the circulating apoL-I/Hpr-containing HDL particles.

摘要

触珠蛋白相关蛋白(Hpr)是一种灵长类动物特有的血浆蛋白,与含载脂蛋白L-I(apoL-I)的高密度脂蛋白(HDL)颗粒相关,被证明是天然免疫防御的一部分。尽管此前一直认为Hpr不与血红蛋白结合,但本研究表明,重组Hpr与血红蛋白的结合效率与触珠蛋白(Hp)一样高。然而,与Hp不同的是,Hpr不会促进与清道夫受体CD163的任何高亲和力结合。血浆Hpr与apoL-I的血红蛋白亲和沉淀表明血红蛋白与掺入HDL组分中的循环天然Hpr结合。总之,血浆中有两种而不是一种具有高亲和力的血红蛋白结合触珠蛋白,但只有Hp-血红蛋白复合物能被CD163有效识别。因此,在测量“游离”血浆血红蛋白时应考虑循环中与Hpr结合的血红蛋白。此外,与Hpr结合的血红蛋白可能有助于含apoL-I/Hpr的循环HDL颗粒的生物活性。

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