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本文引用的文献

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Plasma clearance of rat bikunin: evidence for receptor-mediated uptake.大鼠 bikunin 的血浆清除率:受体介导摄取的证据。
Biochem J. 1995 Jun 15;308 ( Pt 3)(Pt 3):881-7. doi: 10.1042/bj3080881.
2
Effects of exogenous hyaluronic acid and serum on matrix organization and stability in the mouse cumulus cell-oocyte complex.外源性透明质酸和血清对小鼠卵丘细胞-卵母细胞复合体中基质组织和稳定性的影响。
J Biol Chem. 1993 Sep 25;268(27):20473-81.
3
TSG-6: a TNF-, IL-1-, and LPS-inducible secreted glycoprotein associated with arthritis.TSG-6:一种与关节炎相关的肿瘤坏死因子、白细胞介素-1和脂多糖诱导分泌的糖蛋白。
J Immunol. 1993 Dec 1;151(11):6593-601.
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Characterization of the cellular binding site for the urinary trypsin inhibitor.
J Biol Chem. 1994 Aug 12;269(32):20642-7.
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The lipocalin protein family: a role in cell regulation.脂质运载蛋白家族:在细胞调节中的作用。
FEBS Lett. 1994 Oct 31;354(1):7-11. doi: 10.1016/0014-5793(94)01078-1.
6
Comparative mapping of lipocalin genes in human and mouse: the four genes for complement C8 gamma chain, prostaglandin-D-synthase, oncogene-24p3, and progestagen-associated endometrial protein map to HSA9 and MMU2.人源和鼠源脂质运载蛋白基因的比较图谱:补体C8γ链、前列腺素-D-合酶、癌基因-24p3和孕激素相关子宫内膜蛋白的四个基因定位于人9号染色体和小鼠2号染色体。
Genomics. 1994 Sep 1;23(1):145-50. doi: 10.1006/geno.1994.1470.
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cDNA and deduced amino acid sequence of human PK-120, a plasma kallikrein-sensitive glycoprotein.
FEBS Lett. 1995 Jan 3;357(2):207-11. doi: 10.1016/0014-5793(94)01364-7.
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Cloning and characterization of cDNA for inter-alpha-trypsin inhibitor family heavy chain-related protein (IHRP), a novel human plasma glycoprotein.
J Biochem. 1995 Jan;117(1):14-8. doi: 10.1093/oxfordjournals.jbchem.a124701.
9
Inhibitory effect of a conjugate between human urokinase and urinary trypsin inhibitor on tumor cell invasion in vitro.人尿激酶与尿胰蛋白酶抑制剂偶联物对体外肿瘤细胞侵袭的抑制作用
J Biol Chem. 1995 Apr 7;270(14):8361-6. doi: 10.1074/jbc.270.14.8361.
10
Mouse alpha-1-microglobulin/bikunin precursor: cDNA analysis, gene evolution and physical assignment of the gene next to the orosomucoid locus.小鼠α-1-微球蛋白/比库宁前体:cDNA分析、基因进化以及该基因在类粘蛋白基因座旁的物理定位。
Biochim Biophys Acta. 1993 Aug 19;1174(2):195-200. doi: 10.1016/0167-4781(93)90115-t.

α-抑制因子家族:从结构到调控

The inter-alpha-inhibitor family: from structure to regulation.

作者信息

Salier J P, Rouet P, Raguenez G, Daveau M

机构信息

INSERM Unit-78 and Institut Fédératif de Recherches Multidisciplinaires sur les Peptides, Boisguillaume, France.

出版信息

Biochem J. 1996 Apr 1;315 ( Pt 1)(Pt 1):1-9. doi: 10.1042/bj3150001.

DOI:10.1042/bj3150001
PMID:8670091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1217155/
Abstract

Inter-alpha-inhibitor (IalphaI) and related molecules, collectively referred to as the IalphaI family, are a group of plasma protease inhibitors. They display attractive features such as precursor polypeptides that give rise to mature chains with quite distinct fates and functions, and inter-chain glycosaminoglycan bonds within the various molecules. The discovery of an ever growing number of such molecules has raised pertinent questions about their pathophysiological functions. The knowledge of this family has long been structure-oriented, whereas the structure/function and structure/regulation relationships of the family members and their genes have been largely ignored. These relationships are now being elucidated in events such as gene transcription, precursor processing, changes in plasma protein levels in health and disease and binding capacities that involve hyaluronan as well as other plasma proteins as ligands. This review presents some recent progress made in these fields that paves the way for an understanding of the functions of IalphaI family members in vivo. Finally, given the wealth of heterogeneous, complicated and sometimes contradictory nomenclatures and acronyms currently in use for this family, a new, uniform, nomenclature is proposed for IalphaI family genes, precursor polypeptides and assembled proteins.

摘要

α-间抑制因子(IαI)及相关分子,统称为IαI家族,是一组血浆蛋白酶抑制剂。它们具有一些吸引人的特性,例如前体多肽可产生具有截然不同命运和功能的成熟链,以及不同分子内的链间糖胺聚糖键。越来越多此类分子的发现引发了关于其病理生理功能的相关问题。长期以来,对这个家族的认识一直以结构为导向,而家族成员及其基因的结构/功能和结构/调控关系在很大程度上被忽视了。现在,在诸如基因转录、前体加工、健康和疾病状态下血浆蛋白水平的变化以及涉及透明质酸和其他血浆蛋白作为配体的结合能力等事件中,这些关系正在得到阐明。本综述介绍了这些领域最近取得的一些进展,为理解IαI家族成员在体内的功能铺平了道路。最后,鉴于目前该家族使用的大量异质、复杂且有时相互矛盾的命名法和首字母缩略词,本文提出了一种新的、统一的IαI家族基因、前体多肽和组装蛋白的命名法。