Department of Pharmaceutical Sciences, School of Pharmacy, North Dakota State University, Sudro Hall, Room 203, Fargo, ND, 58108-6050, USA.
Department of Animal Sciences, North Dakota State University, Fargo, ND, USA.
Cell Tissue Res. 2019 Jun;376(3):425-432. doi: 10.1007/s00441-019-02995-y. Epub 2019 Feb 2.
The lung tissue contains a heterogeneous milieu of bronchioles, epithelial, airway smooth muscle (ASM), alveolar, and immune cell types. Healthy bronchiole comprises epithelial cells surrounded by ASM cells and helps in normal respiration. In contrast, airway remodeling, or plasticity, increases surrounding of bronchial epithelium during inflammation, especially in asthmatic condition. Given the profound functional difference between ASM, epithelial, and other cell types in the lung, it is imperative to separate and isolate different cell types of lungs for genomics, proteomics, and molecular analysis, which will improve the diagnostic and therapeutic approach to treat cell-specific lung disorders. Laser capture microdissection (LCM) is the technique generally used for the isolation of specific cell populations under direct visual inspection, which plays a crucial role to evaluate cell-specific effect in clinical and preclinical setup. However, maintenance of tissue RNA quality and integrity in LCM studies are very challenging tasks. It is obvious to believe that the major factor affecting the RNA quality is tissue-fixation method. The prime focus of this study was to address the RNA quality factors within the lung tissue using the different solvent system to fix tissue sample to obtain high-quality RNA. Paraformaldehyde and Carnoy's solutions were used for fixing the lung tissue and compared RNA integrity in LCM captured lung tissue samples. To further confirm the quality of RNA, we measured cellular marker genes in collected lung tissue samples from control and mixed allergen (MA)-induced asthmatic mouse model using qRT-PCR technique. RNA integrity number showed a significantly better quality of RNA in lung tissue samples fixed with Carnoy's solution compared to paraformaldehyde solution. Isolated RNA from MA-induced asthmatic murine lung epithelium, smooth muscle, and granulomatous foci using LCM showed a significant increase in remodeling gene expression compared to control which confirm the quality and integrity of isolated RNA. Overall, the study concludes tissue fixation solvent can alter the quality of RNA in the lung and the outcome of the results.
肺组织包含异质的小气道、上皮细胞、气道平滑肌 (ASM)、肺泡和免疫细胞类型。健康的小气道由 ASM 细胞环绕的上皮细胞组成,有助于正常呼吸。相比之下,气道重塑或可塑性会在炎症期间增加支气管上皮周围的细胞数量,尤其是在哮喘情况下。鉴于肺中的 ASM、上皮细胞和其他细胞类型之间存在显著的功能差异,因此必须分离和分离肺的不同细胞类型,用于基因组学、蛋白质组学和分子分析,这将改善针对特定细胞类型的肺部疾病的诊断和治疗方法。激光捕获显微切割 (LCM) 是一种通常用于在直接目视检查下分离特定细胞群体的技术,它在临床和临床前设置中评估细胞特异性效应方面起着至关重要的作用。然而,在 LCM 研究中保持组织 RNA 质量和完整性是非常具有挑战性的任务。显然,影响 RNA 质量的主要因素是组织固定方法。本研究的主要重点是使用不同的溶剂系统固定组织样本,以获得高质量的 RNA,从而解决肺组织内的 RNA 质量因素。使用多聚甲醛和卡诺氏液固定肺组织,并比较 LCM 捕获的肺组织样本中的 RNA 完整性。为了进一步确认 RNA 的质量,我们使用 qRT-PCR 技术测量了来自对照和混合过敏原 (MA) 诱导的哮喘小鼠模型收集的肺组织样本中的细胞标记基因。RNA 完整性数显示,用卡诺氏液固定的肺组织样本的 RNA 质量明显更好。使用 LCM 从小鼠哮喘模型的肺上皮细胞、平滑肌和肉芽肿焦点中分离的 RNA 显示,与对照相比,重塑基因的表达显著增加,这证实了分离 RNA 的质量和完整性。总体而言,该研究得出结论,组织固定溶剂可以改变肺组织中的 RNA 质量和结果。