华支睾吸虫葡萄糖摄取过程中葡萄糖转运蛋白4的功能表征。

0 PARASITOLOGY
Parasites, hosts and diseases Pub Date : 2024-11-01 Epub Date: 2024-11-22 DOI:10.3347/PHD.24051
Hojong Jun, Ernest Mazigo, Wang-Jong Lee, Yun-Kyu Park, Jin-Hee Han, Seok Ho Cha
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引用次数: 0

摘要

引起华支睾吸虫病的华支睾吸虫病在东亚国家普遍存在,并造成显著的健康风险,包括胆管并发症。尽管吡喹酮是该病的主要治疗方法,但吸虫中出现的耐药性突出表明需要采取替代策略。了解包括中华滴虫在内的吸虫的营养吸收机制,对于开发未来有效的治疗方法至关重要。本研究旨在利用合成的sinensis成虫的cDNA,研究sinensis葡萄糖转运蛋白4 (CsGTP4)的功能,并确定其在sinensis成虫营养摄取中的作用。CsGTP4的功能表征包括将其cRNA注射到非洲爪蟾卵母细胞中并分析脱氧d -葡萄糖摄取水平。结果表明,脱氧d -葡萄糖摄取依赖于脱氧d -葡萄糖孵育和CsGTP4表达时间,但不依赖于钠。浓度依赖性摄取遵循Michaelis-Menten方程,根据Lineweaver-Burk分析,Km值为2.7 mM, Vmax值为476 pmol/卵母细胞/h。未观察到放射性标记的α-酮戊二酸盐、对氨基马来酸盐、牛磺胆酸盐、精氨酸或肉毒碱的摄取。未标记的葡萄糖和半乳糖显著抑制CsGTP4对脱氧d -葡萄糖的摄取,并呈浓度依赖性。在强酸性和碱性条件下,其活性均受到明显抑制。这些对CsGTP4的葡萄糖摄取动力学和pH依赖性的见解为吸虫的营养获取提供了更深入的了解。这项研究有助于开发新的抗寄生虫药物,解决受影响地区的重大社会经济挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional characterization of glucose transporter 4 involved in glucose uptake in Clonorchis sinensis.

Clonorchis sinensis, which causes clonorchiasis, is prevalent in East Asian countries and poses notable health risks, including bile duct complications. Although praziquantel is the primary treatment for the disease, the emerging resistance among trematodes highlights the need for alternative strategies. Understanding the nutrient uptake mechanisms in trematodes, including C. sinensis, is crucial for developing future effective treatments. This study aimed to characterize the function of C. sinensis glucose transporter 4 (CsGTP4) and determine its role in nutrient uptake employing synthesized cDNA of adult C. sinensis worms. The functional characterization of CsGTP4 involved injecting its cRNA into Xenopus laevis oocytes and analyzing the deoxy-D-glucose uptake levels. The results demonstrated that deoxy-D-glucose uptake depended on the deoxy-D-glucose incubation and CsGTP4 expression time, but not sodium-dependent. The concentration-dependent uptake followed the Michaelis-Menten equation, with a Km value of 2.7 mM and a Vmax value of 476 pmol/oocyte/h based on the Lineweaver-Burk analysis. No uptake of radiolabeled α-ketoglutarate, p-aminohippurate, taurocholate, arginine, or carnitine was observed. The uptake of deoxy-D-glucose by CsGTP4 was significantly inhibited by unlabeled glucose and galactose in a concentration-dependent manner. It was significantly inhibited under strongly acidic and basic conditions. These insights into the glucose uptake kinetics and pH dependency of CsGTP4 provide a deeper understanding of nutrient acquisition in trematodes. This study contributes to the development of novel antiparasitic agents, addressing a considerable socioeconomic challenge in affected regions.

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2.70
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