成人心室组织低温保存制备活心肌切片的研究

Alessandra M. Lodrini, Esmee J. Groeneveld, Meindert Palmen, Jesper Hjortnaes, Anke M. Smits, Marie-José Goumans
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引用次数: 0

摘要

活体心肌切片(LMS)是可以在培养中维持的成人心肌超薄切片。这些切片为研究心肌细胞(CMs)、其他心脏细胞类型和细胞外基质之间的相互作用提供了一个独特的平台,同时在较长时间内维持CMs的细胞结构和电表型。尽管LMS比其他心脏模型有优势,但它也有局限性,特别是对切片质量的依赖。影响切片质量的主要因素是处理心脏组织块的方法。目前的方法通常需要在切除组织块后立即准备切片,这限制了实验的时间。为了解决这一限制,我们开发了一种简单的成人心肌冷冻保存程序,允许在后期制备LMS。该方案提供了所需设备和试剂的清单,以及处理心肌和切片制备的方法的详细描述。我们提出的典型结果表明,冷冻保存的人类心脏组织保留生物量和结构完整性,可与新鲜获得的心肌相媲美。此外,我们评估了来自新鲜和冷冻保存样品的LMS。组织学分析证实,在没有电刺激的情况下,培养24小时至5天后,所有LMS的存活能力、正常细胞形态和CMs之间的间隙连接都得到了保留。低温保存延长了组织收集和LMS制备之间的间隔,便于进行更长期和更复杂的实验。进一步研究冷冻保存对各种心脏细胞类型的影响,将促进更好的供体器官管理和有效地储存来自众多供体和疾病状态的心脏样本。©2024作者。Wiley期刊有限公司发表的现行方案:基本方案1:制备和保存成人心肌基本方案2:从冷冻保存的心肌块中制备成人活心肌切片
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cryopreservation of Human Adult Ventricular Tissue for the Preparation of Viable Myocardial Slices

Cryopreservation of Human Adult Ventricular Tissue for the Preparation of Viable Myocardial Slices

Living myocardial slices (LMS) are ultrathin sections of adult myocardium that can be maintained in culture. These slices provide a unique platform for studying interactions between cardiomyocytes (CMs), other cardiac cell types, and the extracellular matrix while maintaining the cytoarchitecture and electrical phenotype of CMs over extended periods. Despite their advantages over other cardiac models, LMS have limitations, particularly their reliance on slice quality. The primary factor influencing the quality of the slices is the method used to process the cardiac tissue block. Current methods typically require immediate slice preparation following the excision of the tissue block, which restricts the timing of experiments. To address this limitation, we developed a simple procedure for cryopreserving human adult myocardium, allowing the preparation of LMS at a later stage. The protocol provides a list of required equipment and reagents, as well as a detailed description of the methodology for processing the myocardium and slice preparation. We present typical results demonstrating that cryopreserved human cardiac tissue retains biomass and structural integrity comparable to freshly obtained myocardium. Furthermore, we assessed the LMS derived from both fresh and cryopreserved samples. Histological analysis confirmed the preservation of viability, normal cytomorphology, and gap junctions between CMs in all LMS after 24 h and up to 5 days of culture in the absence of electrical stimulation. Cryopreservation extends the interval between tissue collection and LMS preparation, facilitating longer-term and more complex experiments. Further research into the impact of cryopreservation on various cardiac cell types will promote better donor organ management and efficient banking of cardiac samples from a multitude of donors and disease states. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Preparation and preservation of human adult myocardium

Basic Protocol 2: Preparation of adult living myocardial slices from cryopreserved blocks

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