The Development of an Animal Product-free, Precision-cut Lung Slice Cryopreservation and Post-thaw Culture Method.

IF 3 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Atla-Alternatives To Laboratory Animals Pub Date : 2025-05-01 Epub Date: 2025-04-27 DOI:10.1177/02611929251336446
Holger P Behrsing, Khalid Amin, David Allen, Joseph Hughes, McKenzie Obermok, Vivek Patel
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引用次数: 0

Abstract

As new approach methodologies (NAMs) are increasingly explored to identify dependable and accurate non-animal alternatives to predict human toxicities, several 3-D test systems have emerged as excellent models of the human respiratory tract. Among these, human precision-cut lung slices (hPCLS) are considered highly relevant, as they contain many cell types (including key immune cells), feature small airway structures and boast native respiratory parenchymal architecture. However, a lack of long-term preservation methods has hampered the use of the hPCLS model for repeat and mainstream testing. In the current study, a range of potential methods were progressively evaluated for the optimum recovery of hPCLS after thawing and multi-week culturing. These methods featured: five different cryopreservation buffer (CB) recipes; freezing either before or after culture initiation; two culture media (based on E-199 and DMEM/F12); and two culture maintenance methods (submerged and air-liquid interface (ALI)). Endpoints used for the assessment of hPCLS culture health included the WST-8 viability assay, protein content and H&E histology of slice sections. Two of the CBs and immediate cryopreservation after slicing produced hPCLS with higher post-thaw viability. While both media recipes and culture methods maintained high slice viability for approximately 2 weeks, the use of DMEM-F12-based medium in ALI culture was superior for the 3-week cultures. Applying due diligence to hPCLS cryopreservation and post-thaw method development provides researchers with an underutilised human respiratory model. Studies making use of cryopreserved banks of normal or diseased tissues (from a diverse demographic pool of donors) can now be initiated as desired, repeated, or expanded upon to interrogate numerous aspects of physiology, toxicology and drug efficacy. These can be applied as routine screening applications or complex evaluations, including those benefitting a regulatory setting.

一种无动物制品、精密切割的肺片冷冻保存和解冻后培养方法的建立。
随着人们越来越多地探索新的方法(NAMs)来确定可靠和准确的非动物替代品来预测人类毒性,一些3d测试系统已经成为人类呼吸道的优秀模型。其中,人类精确肺切片(hPCLS)被认为是高度相关的,因为它们包含许多细胞类型(包括关键免疫细胞),具有小气道结构和天然呼吸实质结构。然而,长期保存方法的缺乏阻碍了hPCLS模型在重复和主流检测中的应用。在目前的研究中,我们逐步评估了一系列潜在的方法,以获得解冻和多周培养后hPCLS的最佳恢复。这些方法的特点是:五种不同的低温保存缓冲液(CB)配方;在开始培养之前或之后进行冷冻;两种培养基(基于E-199和DMEM/F12);以及两种培养维护方法(浸没和气液界面(ALI))。用于评估hcls培养健康的终点包括WST-8活力测定、蛋白质含量和切片H&E组织学。两个CBs和切片后立即冷冻保存产生具有较高解冻后活力的hPCLS。虽然两种培养基配方和培养方法都能保持大约2周的高切片活力,但在ALI培养中使用基于dmem - f12的培养基在3周的培养中具有优势。对hPCLS冷冻保存和解冻后方法开发进行尽职调查,为研究人员提供了一个未充分利用的人类呼吸模型。利用冷冻保存的正常或病变组织库(来自不同的捐赠者)的研究现在可以根据需要启动,重复或扩展,以询问生理学,毒理学和药物功效的许多方面。这些可以应用于常规筛选应用或复杂评估,包括那些有利于监管设置的应用。
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来源期刊
CiteScore
3.80
自引率
3.70%
发文量
60
审稿时长
>18 weeks
期刊介绍: Alternatives to Laboratory Animals (ATLA) is a peer-reviewed journal, intended to cover all aspects of the development, validation, implementation and use of alternatives to laboratory animals in biomedical research and toxicity testing. In addition to the replacement of animals, it also covers work that aims to reduce the number of animals used and refine the in vivo experiments that are still carried out.
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