INSERM U618, Protéases et Vectorisation Pulmonaires, IFR 135 Imagerie Fonctionnelle, Université François Rabelais, Tours, France.
Biochimie. 2010 Nov;92(11):1568-79. doi: 10.1016/j.biochi.2010.03.011. Epub 2010 Mar 24.
Two kininogens are found in mammalian sera: HK (high molecular weight kininogen) and LK (low molecular weight kininogen) with the exception of the rat which encompasses a third kininogen, T-Kininogen (TK). Kininogens are multifunctional glycosylated molecules related to cystatins (clan IH, family I25). They harbor three cystatin domains but only two of them are tight-binding inhibitors of cysteine cathepsins. HK and LK, but not TK, are precursors of potent peptide hormones, the kinins, which are released proteolytically by tissue and plasma kallikreins. Besides these classical features novel functions of kininogens have been recently discovered; they are described in the second part of this review. HKa, which corresponds to the kinin-free two-chain HK and its isolated domain D5 (kininostatin), possesses angiostatic and pro-apoptotic properties, inhibits the proliferation of endothelial cells and participates in the regulation of angiogenesis. Moreover, some HK-derived peptides display potent and broad-spectrum microbicidal properties against both Gram-positive and Gram-negative bacteria, and thus may offer a promising alternative to conventional antibiotic therapy. Of seminal interest, a kininogen-derived peptide inhibits activation of the contact phase system of coagulation and protects mice with invasive Streptococcus pyogenes infection from pulmonary lesions. On the other hand, TK is a biomarker of aging at the end of lifespan of elderly rats. However, although TK has been initially identified as an acute phase reactant, and earlier known as alpha-l-acute phase globulin, the increase of TK in liver and plasma is not known to relate to any inflammatory event during the senescence process.
高分子量激肽原(HK)和低分子量激肽原(LK),除大鼠外,大鼠还包含第三种激肽原,即 T 激肽原(TK)。激肽原是与半胱氨酸蛋白酶抑制剂(家族 I25)相关的多功能糖基化分子。它们含有三个半胱氨酸蛋白酶抑制剂结构域,但只有两个是半胱氨酸蛋白酶的紧密结合抑制剂。HK 和 LK,但不是 TK,是强效肽激素激肽的前体,这些激肽通过组织和血浆激肽释放酶蛋白水解释放。除了这些经典特征外,激肽原的新功能最近也被发现;在这篇综述的第二部分中对它们进行了描述。HKA 对应于无激肽的二链 HK 和其分离的结构域 D5(激肽抑制素),具有血管生成抑制和促凋亡特性,抑制内皮细胞的增殖,并参与血管生成的调节。此外,一些 HK 衍生肽对革兰氏阳性和革兰氏阴性细菌具有强大且广谱的杀菌作用,因此可能为传统抗生素治疗提供有前途的替代方案。值得注意的是,一种激肽原衍生肽抑制凝血接触相系统的激活,并保护侵袭性化脓性链球菌感染的小鼠免受肺部损伤。另一方面,TK 是老年大鼠寿命末期衰老的生物标志物。然而,尽管 TK 最初被鉴定为急性期反应物,并且早期被称为α-1-急性期球蛋白,但肝脏和血浆中 TK 的增加与衰老过程中的任何炎症事件都没有关系。