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小鼠体内α2-抗纤溶酶-蛋白酶复合物血浆清除的独特途径。

A unique pathway for the plasma elimination of alpha 2-antiplasmin-protease complexes in mice.

作者信息

Gonias S L, Fuchs H E, Pizzo S V

出版信息

Thromb Haemost. 1982 Oct 29;48(2):208-10.

PMID:6758181
Abstract

Radiolabeled alpha 2-antiplasmin cleared slowly from the circulation of mice. Complex formation with either plasmin or trypsin resulted in a significant increase in the plasma elimination rate of the protease inhibitor. Approximately 20 min and 14 min were required for 50% of the injected alpha 2-antiplasmin-plasmin and alpha 2-antiplasmin-trypsin to clear from the circulation, respectively. Significant competition was observed when radiolabeled alpha 2-antiplasmin-plasmin was cleared in the presence of a large molar excess of unlabeled alpha 2-antiplasmin-plasmin. alpha 1-Antitrypsin-trypsin failed to complete with radiolabeled alpha 2-antiplasmin-plasmin even when present at 2000 fold molar excess. Organ distribution studies localized the major site of alpha 2-antiplasmin-plasmin clearance in the liver. Microscopic autoradiography data suggested that the cell responsible for the clearance pathway was the hepatocyte.

摘要

放射性标记的α2-抗纤溶酶从小鼠循环系统中清除缓慢。与纤溶酶或胰蛋白酶形成复合物会导致蛋白酶抑制剂的血浆清除率显著增加。分别约需20分钟和14分钟,注射的α2-抗纤溶酶-纤溶酶和α2-抗纤溶酶-胰蛋白酶的50%才能从循环中清除。当在大量摩尔过量的未标记α2-抗纤溶酶-纤溶酶存在的情况下清除放射性标记的α2-抗纤溶酶-纤溶酶时,观察到显著的竞争。即使α1-抗胰蛋白酶-胰蛋白酶以2000倍摩尔过量存在,也无法与放射性标记的α2-抗纤溶酶-纤溶酶竞争。器官分布研究确定肝脏是α2-抗纤溶酶-纤溶酶清除的主要部位。显微放射自显影数据表明,负责清除途径的细胞是肝细胞。

相似文献

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A unique pathway for the plasma elimination of alpha 2-antiplasmin-protease complexes in mice.小鼠体内α2-抗纤溶酶-蛋白酶复合物血浆清除的独特途径。
Thromb Haemost. 1982 Oct 29;48(2):208-10.
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Kinetics of the inhibition of plasmin in acidified human plasma.酸性人血浆中纤溶酶抑制作用的动力学
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An enzyme-linked immunosorbent assay (ELISA) for the measurement of plasmin-alpha 2-antiplasmin complex in human plasma--application to the detection of in vivo activation of the fibrinolytic system.一种用于检测人血浆中纤溶酶-α2-抗纤溶酶复合物的酶联免疫吸附测定法(ELISA)——在纤溶系统体内激活检测中的应用
Thromb Haemost. 1986 Oct 21;56(2):124-7.
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Catabolic pathways for streptokinase, plasmin, and streptokinase activator complex in mice. In vivo reaction of plasminogen activator with alpha 2-macroglobulin.小鼠中链激酶、纤溶酶及链激酶激活剂复合物的分解代谢途径。纤溶酶原激活剂与α2-巨球蛋白的体内反应。
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Alpha 2-antiplasmin Enschede is not an inhibitor, but a substrate, of plasmin.α2-抗纤溶酶恩斯赫德不是纤溶酶的抑制剂,而是其底物。
Biochem J. 1988 Oct 15;255(2):609-15.
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[Hepatocyte receptors for proteinase inhibitor complexes with plasmin].[蛋白酶抑制剂与纤溶酶复合物的肝细胞受体]
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Alpha 2-macroglobulin is the primary inhibitor of miniplasmin in vitro and in vivo in the mouse. Comparison with alpha 2-antiplasmin in simultaneous reaction experiments.α2-巨球蛋白是小鼠体内外微小纤溶酶的主要抑制剂。在同步反应实验中与α2-抗纤溶酶的比较。
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Assessment of the relative contribution of different protease inhibitors to the inhibition of plasmin in vivo.评估不同蛋白酶抑制剂在体内对纤溶酶抑制作用的相对贡献。
Thromb Haemost. 1993 Feb 1;69(2):141-6.
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Antiplasmin: the forgotten serpin?抗纤溶酶:被遗忘的丝氨酸蛋白酶抑制剂?
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The autoimmune blistering skin disease bullous pemphigoid. The presence of plasmin/alpha 2-antiplasmin complexes in skin blister fluid indicates plasmin generation in lesional skin.自身免疫性水疱性皮肤病大疱性类天疱疮。皮肤水疱液中存在纤溶酶/α2-抗纤溶酶复合物表明皮损部位有纤溶酶生成。
J Clin Invest. 1993 Aug;92(2):978-83. doi: 10.1172/JCI116674.

引用本文的文献

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Low-density lipoprotein receptor-related protein 1 is an essential receptor for myelin phagocytosis.低密度脂蛋白受体相关蛋白1是髓鞘吞噬作用的必需受体。
J Cell Sci. 2009 Apr 15;122(Pt 8):1155-62. doi: 10.1242/jcs.040717. Epub 2009 Mar 19.
2
Assignment of a single disulphide bridge in human alpha2-antiplasmin: implications for the structural and functional properties.人α2-抗纤溶酶中单个二硫键的定位:对结构和功能特性的影响
Biochem J. 1997 May 1;323 ( Pt 3)(Pt 3):847-52. doi: 10.1042/bj3230847.
3
A nonantigenic covalent streptokinase-polyethylene glycol complex with plasminogen activator function.
一种具有纤溶酶原激活剂功能的非抗原性共价链激酶 - 聚乙二醇复合物。
J Clin Invest. 1985 Feb;75(2):413-9. doi: 10.1172/JCI111715.
4
Alpha 2-macroglobulin is the primary inhibitor of miniplasmin in vitro and in vivo in the mouse. Comparison with alpha 2-antiplasmin in simultaneous reaction experiments.α2-巨球蛋白是小鼠体内外微小纤溶酶的主要抑制剂。在同步反应实验中与α2-抗纤溶酶的比较。
Biochem J. 1988 Oct 15;255(2):725-30.
5
A common neoepitope is created when the reactive center of C1-inhibitor is cleaved by plasma kallikrein, activated factor XII fragment, C1 esterase, or neutrophil elastase.当C1抑制剂的反应中心被血浆激肽释放酶、活化的因子XII片段、C1酯酶或中性粒细胞弹性蛋白酶切割时,会产生一种常见的新表位。
J Clin Invest. 1988 Aug;82(2):700-5. doi: 10.1172/JCI113650.
6
Human plasma kallikrein and C1 inhibitor form a complex possessing an epitope that is not detectable on the parent molecules: demonstration using a monoclonal antibody.人血浆激肽释放酶与C1抑制剂形成一种复合物,该复合物具有在其母体分子上无法检测到的表位:使用单克隆抗体的证明。
Proc Natl Acad Sci U S A. 1985 Aug;82(15):5190-3. doi: 10.1073/pnas.82.15.5190.