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探索临床前研究的维度:3D培养作为恰加斯病心脏纤维化的研究模型

Exploring the Dimensions of Pre-Clinical Research: 3D Cultures as an Investigative Model of Cardiac Fibrosis in Chagas Disease.

作者信息

Seydel Clara Monteiro, Gonzaga Beatriz Matheus de Souza, Coelho Laura Lacerda, Garzoni Luciana Ribeiro

机构信息

Laboratório de Inovações em Terapias, Ensino e Bioprodutos, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz, Rio de Janeiro 21040-360, Brazil.

出版信息

Biomedicines. 2024 Jun 25;12(7):1410. doi: 10.3390/biomedicines12071410.

Abstract

A three-dimensional (3D) cell culture can more precisely mimic tissues architecture and functionality, being a promising alternative model to study disease pathophysiology and drug screening. Chagas disease (CD) is a neglected parasitosis that affects 7 million people worldwide. () mechanisms of invasion/persistence continue to be elucidated. Benznidazole (BZ) and Nifurtimox (NF) are trypanocidal drugs with few effects on the clinical manifestations of the chronic disease. Chronic Chagas cardiomyopathy (CCC) is the main manifestation of CD due to its frequency and severity. The development of fibrosis and hypertrophy in cardiac tissue can lead to heart failure and sudden death. Thus, there is an urgent need for novel therapeutic options. Our group has more than fifteen years of expertise using 3D primary cardiac cell cultures, being the first to reproduce fibrosis and hypertrophy induced by infection in vitro. These primary cardiac spheroids exhibit morphological and functional characteristics that are similar to heart tissue, making them an interesting model for studying CD cardiac fibrosis. Here, we aim to demonstrate that our primary cardiac spheroids are great preclinical models which can be used to develop new insights into CD cardiac fibrosis, presenting advances already achieved in the field, including disease modeling and drug screening.

摘要

三维(3D)细胞培养可以更精确地模拟组织架构和功能,是研究疾病病理生理学和药物筛选的一种有前景的替代模型。恰加斯病(CD)是一种被忽视的寄生虫病,全球有700万人受其影响。()侵袭/持续存在的机制仍在不断阐明。苯并硝唑(BZ)和硝呋替莫(NF)是杀锥虫药物,对慢性病的临床表现影响甚微。慢性恰加斯心肌病(CCC)是CD的主要表现,因其发病率和严重程度所致。心脏组织中纤维化和肥大的发展可导致心力衰竭和猝死。因此,迫切需要新的治疗选择。我们团队在使用3D原代心脏细胞培养方面拥有超过十五年的专业经验,是首个在体外重现感染诱导的纤维化和肥大的团队。这些原代心脏球体表现出与心脏组织相似的形态和功能特征,使其成为研究CD心脏纤维化的一个有趣模型。在此,我们旨在证明我们的原代心脏球体是优秀的临床前模型,可用于深入了解CD心脏纤维化,展示该领域已取得的进展,包括疾病建模和药物筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b68/11274318/e5f4cf913303/biomedicines-12-01410-g001.jpg

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