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雅拉卡蛇糖蛋白1b结合蛋白在巴西矛头蝮蛇咬伤时导致血小板减少。

Jararaca GPIb-binding protein causes thrombocytopenia during Bothrops jararaca envenomation.

作者信息

Santoro Marcelo Larami, Sachetto Ana Teresa Azevedo, Rosa Jaqueline Gomes, Torquato Ricardo José Soares, Andrade-Silva Débora, Trevisan-Silva Dilza, de Albuquerque Cynthia Zaccanini, Serrano Solange M T, de Moura Mattaraia Vânia Gomes, Tanaka Aparecida Sadae, Peichoto Maria Elisa

机构信息

Biotério Central, Instituto Butantan, Av. Dr. Vital Brasil, 1500, São Paulo, SP, 05503 - 900, Brazil.

Escola Superior do Instituto Butantan, Av. da Universidade, São Paulo, SP, Brazil.

出版信息

Sci Rep. 2024 Dec 30;14(1):31769. doi: 10.1038/s41598-024-81851-8.

Abstract

Inoculation of Bothrops jararaca snake venom (BjV) induces thrombocytopenia in humans and various animal species. Although several BjV toxins acting on hemostasis have been well characterized in vitro, it is not known which one is responsible for inducing thrombocytopenia in vivo. In previous studies, we showed that BjV incubated with metalloproteinase or serine proteinase inhibitors and/or anti-botrocetin antibodies still induced thrombocytopenia in rats and mice. Thus, herein we identified and characterized BjV toxins responsible for inducing thrombocytopenia. Initially, by filtering BjV on ultrafiltration systems, proteins with molecular masses between 30 and 50 kDa were shown to induce thrombocytopenia in mice, but they were not associated with hemorrhagic or coagulating activities. The 50 kDa ultrafiltrate was chromatographed, and two proteins (named fraction D and fraction E) induced thrombocytopenia in mice. However, neither fraction D nor fraction E induced platelet aggregation in platelet-rich plasma or whole blood from humans or mice. By mass spectrometry analysis, fraction E was identified as jararaca glycoprotein Ib (GPIb)-binding protein. Injection of these fractions caused thrombocytopenia in control or Vwf mice, showing that the axis platelet GPIb - von Willebrand factor is not involved in their biological action in vivo. New studies are necessary to understand how these proteins act in vivo.

摘要

接种巴西矛头蝮蛇毒(BjV)可导致人类和多种动物物种出现血小板减少症。尽管几种作用于止血的BjV毒素在体外已得到充分表征,但尚不清楚哪种毒素在体内导致血小板减少症。在先前的研究中,我们发现与金属蛋白酶或丝氨酸蛋白酶抑制剂和/或抗博曲酶抗体孵育的BjV仍能在大鼠和小鼠中诱导血小板减少症。因此,在本文中我们鉴定并表征了导致血小板减少症的BjV毒素。最初,通过在超滤系统上过滤BjV,发现分子量在30至50 kDa之间的蛋白质可在小鼠中诱导血小板减少症,但它们与出血或凝血活性无关。对50 kDa的超滤物进行色谱分析,两种蛋白质(分别命名为D组分和E组分)在小鼠中诱导血小板减少症。然而,D组分和E组分均未在富含血小板的血浆或来自人类或小鼠的全血中诱导血小板聚集。通过质谱分析,E组分被鉴定为巴西矛头蝮糖蛋白Ib(GPIb)结合蛋白。注射这些组分可在对照小鼠或Vwf小鼠中引起血小板减少症,表明血小板GPIb - 血管性血友病因子轴不参与它们在体内的生物学作用。需要进行新的研究以了解这些蛋白质在体内的作用方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5eb/11686094/e13c575c51ab/41598_2024_81851_Fig1_HTML.jpg

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