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条件培养基蛋白在牛嗜铬细胞模型中的促心律失常作用。

Pro-arrhythmogenic effects of conditioned medium proteins in a model of bovine chromaffin cells.

机构信息

Department of Neuroscience, University of Minnesota, 4-158 Jackson Hall, 321 Church St s.e., Minneapolis, MN55455, USA.

Department of Pharmacology and Therapeutic, Universidad Autónoma de Madrid, Av. Arzobispo Morcillo 4, 28029Madrid, Spain.

出版信息

Parasitology. 2021 Nov;148(13):1612-1623. doi: 10.1017/S003118202100130X. Epub 2021 Aug 13.

Abstract

Asymptomatic sudden death is the principal cause of mortality in Chagas disease. There is little information about molecular mechanisms involved in the pathophysiology of malignant arrhythmias in Chagasic patients. Previous studies have involved Trypanosoma cruzi secretion proteins in the genesis of arrhythmias ex vivo, but the molecular mechanisms involved are still unresolved. Thus, the aim was to determine the effect of these secreted proteins on the cellular excitability throughout to test its effects on catecholamine secretion, sodium-, calcium-, and potassium-conductance and action potential (AP) firing. Conditioned medium was obtained from the co-culture of T. cruzi and Vero cells (African green monkey kidney cells) and ultra-filtered for concentrating immunogenic high molecular weight parasite proteins. Chromaffin cells were assessed with the parasite and Vero cells control medium. Parasite-secreted proteins induce catecholamine secretion in a dose-dependent manner. Additionally, T. cruzi conditioned medium induced depression of both calcium conductance and calcium and voltage-dependent potassium current. Interestingly, this fact was related to the abolishment of the hyperpolarization phase of the AP produced by the parasite medium. Taken together, these results suggest that T. cruzi proteins may be involved in the genesis of pro-arrhythmic conditions that could influence the appearance of malignant arrhythmias in Chagasic patients.

摘要

无症状性猝死是导致恰加斯病患者死亡的主要原因。目前关于恰加斯病患者恶性心律失常病理生理学中涉及的分子机制的信息很少。先前的研究涉及克氏锥虫分泌蛋白在心律失常发生中的作用,但涉及的分子机制仍未解决。因此,本研究旨在通过测试其对儿茶酚胺分泌、钠、钙和钾电导以及动作电位(AP)发放的影响,来确定这些分泌蛋白对细胞兴奋性的影响。将克氏锥虫和 Vero 细胞(非洲绿猴肾细胞)共培养物获得的条件培养基进行超滤,以浓缩免疫原性高分子量寄生虫蛋白。用寄生虫和 Vero 细胞对照培养基评估嗜铬细胞。寄生虫分泌蛋白以剂量依赖的方式诱导儿茶酚胺分泌。此外,T. cruzi 条件培养基诱导钙电流和钙及电压依赖性钾电流的抑制。有趣的是,这一事实与寄生虫培养基产生的 AP 去极化相的消除有关。综上所述,这些结果表明,T. cruzi 蛋白可能参与了致心律失常条件的产生,这可能影响到恰加斯病患者恶性心律失常的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02a/11010060/1019de88c714/S003118202100130X_figAb.jpg

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