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Airway and alveolar epithelial cells in culture.培养中的气道和肺泡上皮细胞。
Eur Respir J. 2019 Nov 7;54(5). doi: 10.1183/13993003.00742-2019. Print 2019 Nov.
2
Embedding of Precision-Cut Lung Slices in Engineered Hydrogel Biomaterials Supports Extended Culture.精密切割肺切片在工程化水凝胶生物材料中的嵌入支持了延长培养。
Am J Respir Cell Mol Biol. 2020 Jan;62(1):14-22. doi: 10.1165/rcmb.2019-0232MA.
3
Inactivation of nuclear histone deacetylases by EP300 disrupts the MiCEE complex in idiopathic pulmonary fibrosis.EP300 通过使核组蛋白去乙酰化酶失活来破坏特发性肺纤维化中的 MiCEE 复合物。
Nat Commun. 2019 May 20;10(1):2229. doi: 10.1038/s41467-019-10066-7.
4
Cellular Senescence: The Trojan Horse in Chronic Lung Diseases.细胞衰老:慢性肺部疾病中的特洛伊木马。
Am J Respir Cell Mol Biol. 2019 Jul;61(1):21-30. doi: 10.1165/rcmb.2018-0410TR.
5
Live imaging of alveologenesis in precision-cut lung slices reveals dynamic epithelial cell behaviour.实时成像技术在精密肺切片中的肺泡发生研究中揭示了动态上皮细胞行为。
Nat Commun. 2019 Mar 12;10(1):1178. doi: 10.1038/s41467-019-09067-3.
6
Generation of Human 3D Lung Tissue Cultures (3D-LTCs) for Disease Modeling.用于疾病建模的人源三维肺组织培养物(3D-LTCs)的生成
J Vis Exp. 2019 Feb 12(144). doi: 10.3791/58437.
7
Small airway hyperresponsiveness in COPD: relationship between structure and function in lung slices.COPD 中的小气道高反应性:肺切片中结构与功能的关系。
Am J Physiol Lung Cell Mol Physiol. 2019 Mar 1;316(3):L537-L546. doi: 10.1152/ajplung.00325.2018. Epub 2019 Jan 10.
8
The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis.mTORC1/4E-BP1 轴在纤维化过程中代表一个关键的信号节点。
Nat Commun. 2019 Jan 2;10(1):6. doi: 10.1038/s41467-018-07858-8.
9
Establishment and Analysis of Tumor Slice Explants As a Prerequisite for Diagnostic Testing.肿瘤切片外植体的建立与分析作为诊断测试的前提条件
J Vis Exp. 2018 Nov 29(141). doi: 10.3791/58569.
10
Differential effects of Nintedanib and Pirfenidone on lung alveolar epithelial cell function in ex vivo murine and human lung tissue cultures of pulmonary fibrosis.尼达尼布和吡非尼酮对肺纤维化体外培养的鼠和人肺组织肺泡上皮细胞功能的差异影响。
Respir Res. 2018 Sep 15;19(1):175. doi: 10.1186/s12931-018-0876-y.

三维精准肺切片的应用和方法。疾病建模与药物发现。

Applications and Approaches for Three-Dimensional Precision-Cut Lung Slices. Disease Modeling and Drug Discovery.

机构信息

Lung Bioengineering and Regeneration, Department of Experimental Medical Science.

Wallenberg Center for Molecular Medicine.

出版信息

Am J Respir Cell Mol Biol. 2020 Jun;62(6):681-691. doi: 10.1165/rcmb.2019-0276TR.

DOI:10.1165/rcmb.2019-0276TR
PMID:31991090
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7401444/
Abstract

Chronic lung diseases (CLDs), such as chronic obstructive pulmonary disease, interstitial lung disease, and lung cancer, are among the leading causes of morbidity globally and impose major health and financial burdens on patients and society. Effective treatments are scarce, and relevant human model systems to effectively study CLD pathomechanisms and thus discover and validate potential new targets and therapies are needed. Precision-cut lung slices (PCLS) from healthy and diseased human tissue represent one promising tool that can closely recapitulate the complexity of the lung's native environment, and recently, improved methodologies and accessibility to human tissue have led to an increased use of PCLS in CLD research. Here, we discuss approaches that use human PCLS to advance our understanding of CLD development, as well as drug discovery and validation for CLDs. PCLS enable investigators to study complex interactions among different cell types and the extracellular matrix in the native three-dimensional architecture of the lung. PCLS further allow for high-resolution (live) imaging of cellular functions in several dimensions. Importantly, PCLS can be derived from diseased lung tissue upon lung surgery or transplantation, thus allowing the study of CLDs in living human tissue. Moreover, CLDs can be modeled in PCLS derived from normal lung tissue to mimic the onset and progression of CLDs, complementing studies in end-stage diseased tissue. Altogether, PCLS are emerging as a remarkable tool to further bridge the gap between target identification and translation into clinical studies, and thus open novel avenues for future precision medicine approaches.

摘要

慢性肺部疾病(CLD),如慢性阻塞性肺疾病、间质性肺疾病和肺癌,是全球发病率的主要原因之一,给患者和社会带来了重大的健康和经济负担。有效的治疗方法稀缺,需要相关的人类模型系统来有效地研究 CLD 发病机制,从而发现和验证潜在的新靶点和治疗方法。来自健康和患病人体组织的离体肺切片(PCLS)代表了一种很有前途的工具,可以很好地模拟肺部自然环境的复杂性,最近,人类组织的方法和获取途径的改进,导致 PCLS 在 CLD 研究中的应用增加。在这里,我们讨论了使用人离体肺切片来促进我们对 CLD 发展的理解的方法,以及 CLD 的药物发现和验证。PCLS 使研究人员能够研究不同细胞类型和细胞外基质之间在肺部自然三维结构中的复杂相互作用。PCLS 进一步允许对细胞功能进行高分辨率(实时)成像。重要的是,PCLS 可以从肺部手术后或移植的病变肺组织中获得,从而可以在活体人组织中研究 CLD。此外,CLD 可以在源自正常肺组织的 PCLS 中建模,以模拟 CLD 的发作和进展,补充对终末期病变组织的研究。总之,PCLS 正在成为一个非常有前途的工具,进一步弥合了目标识别与转化为临床研究之间的差距,从而为未来的精准医学方法开辟了新的途径。