Increased iron uptake in the bladder wall of racemose cysts of Taenia solium

IF 1.4 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular and biochemical parasitology Pub Date : 2022-09-01 DOI:10.1016/j.molbiopara.2022.111496
Miguel A. Orrego , Carlos M. Vasquez , Kayla Togneri , Juan P. Laclette , Hector H. Garcia , Theodore E. Nash , for the Cysticercosis Working Group in Peru
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引用次数: 1

Abstract

Racemose neurocysticercosis is an aggressive infection caused by the aberrant expansion and proliferation of the bladder wall of the Taenia solium cyst within the subarachnoid spaces of the human brain. The parasite develops and proliferates in a microenvironment with low concentrations of growth factors and micronutrients compared to serum. Iron is important for essential biological processes, but its requirement for racemose cyst viability and proliferation has not been studied. The presence of iron in the bladder wall of racemose and normal univesicular T. solium cysts was determined using Prussian blue staining. Iron deposits were readily detected in the bladder wall of racemose cysts but were not detectable in the bladder wall of univesicular cysts. Consistent with this finding, the genes for two iron-binding proteins (ferritin and melanotransferrin) and ribonucleotide reductase were markedly overexpressed in the racemose cyst compared to univesicular cysts. The presence of iron in the bladder wall of racemose cysts may be due to its increased metabolic rate due to proliferation.

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猪带绦虫总状囊肿膀胱壁铁摄取增加
总状神经囊虫病是一种侵袭性感染,由人类大脑蛛网膜下腔内的猪带绦虫囊肿膀胱壁异常扩张和增殖引起。与血清相比,寄生虫在生长因子和微量营养素浓度较低的微环境中发育和增殖。铁在重要的生物过程中是重要的,但其对总状囊肿生存和增殖的需求尚未研究。用普鲁士蓝染色法测定总状囊性和正常单泡性梭状囊性膀胱壁铁的存在。总状囊肿膀胱壁易检出铁质沉积,而单囊性囊肿膀胱壁未检出铁质沉积。与这一发现一致的是,与单囊性囊肿相比,总状囊肿中两种铁结合蛋白(铁蛋白和黑素转铁蛋白)和核糖核苷酸还原酶的基因明显过表达。总状囊肿膀胱壁铁的存在可能是由于其增殖引起的代谢速率增加。
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来源期刊
CiteScore
2.90
自引率
0.00%
发文量
51
审稿时长
63 days
期刊介绍: The journal provides a medium for rapid publication of investigations of the molecular biology and biochemistry of parasitic protozoa and helminths and their interactions with both the definitive and intermediate host. The main subject areas covered are: • the structure, biosynthesis, degradation, properties and function of DNA, RNA, proteins, lipids, carbohydrates and small molecular-weight substances • intermediary metabolism and bioenergetics • drug target characterization and the mode of action of antiparasitic drugs • molecular and biochemical aspects of membrane structure and function • host-parasite relationships that focus on the parasite, particularly as related to specific parasite molecules. • analysis of genes and genome structure, function and expression • analysis of variation in parasite populations relevant to genetic exchange, pathogenesis, drug and vaccine target characterization, and drug resistance. • parasite protein trafficking, organelle biogenesis, and cellular structure especially with reference to the roles of specific molecules • parasite programmed cell death, development, and cell division at the molecular level.
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