Limjunyawong Nathachit, Mock Jason, Mitzner Wayne
Bloomberg School of Public Health, Environmental Health Sciences, Johns Hopkins University.
Department of Medicine, Pulmonary Diseases and Critical Care Medicine, University of North Carolina School of Medicine.
J Vis Exp. 2015 Aug 31(102):e52964. doi: 10.3791/52964.
The ability to instill live agents, cells, or chemicals directly into the lung without injuring or killing the mice is an important tool in lung cancer research. Although there are a number of methods that have been published showing how to intubate mice for pulmonary function measurements, none are without potential problems for rapid tracheal instillation in large cohorts of mice. In the present paper, a simple and quick method is described that enables an investigator to carry out such instillations in an efficient manner. The method does not require any special tools or lighting and can be learned with very little practice. It involves anesthetizing a mouse, making a small incision in the neck to visualize the trachea, and then inserting an intravenous catheter directly. The small incision is quickly closed with tissue adhesive, and the mice are allowed to recover. A skilled student or technician can do instillations at an average rate of 2 min/mouse. Once the cancer is established, there is frequently a need for quantitative histologic analysis of the lungs. Traditionally pathologists usually do not bother to standardize lung inflation during fixation, and analyses are often based on a scoring system that can be quite subjective. While this may sometime be sufficiently adequate for gross estimates of the size of a lung tumor, any proper stereological quantification of lung structure or cells requires a reproducible fixation procedure and subsequent lung volume measurement. Here we describe simple reliable procedures for both fixing the lungs under pressure and then accurately measuring the fixed lung volume. The only requirement is a laboratory balance that is accurate over a range of 1 mg-300 g. The procedures presented here thus could greatly improve the ability to create, treat, and analyze lung cancers in mice.
在不伤害或杀死小鼠的情况下,将活的病原体、细胞或化学物质直接注入肺部的能力是肺癌研究中的一项重要工具。尽管已经发表了许多关于如何为小鼠插管以进行肺功能测量的方法,但对于在大量小鼠中进行快速气管内滴注而言,这些方法都存在潜在问题。在本文中,我们描述了一种简单快速的方法,使研究人员能够高效地进行此类滴注。该方法不需要任何特殊工具或照明,只需很少的练习就能学会。它包括麻醉小鼠,在颈部做一个小切口以暴露气管,然后直接插入一根静脉导管。小切口用组织粘合剂迅速闭合,让小鼠恢复。一名熟练的学生或技术人员平均每只小鼠滴注时间为2分钟。一旦建立了癌症模型,通常需要对肺部进行定量组织学分析。传统上,病理学家在固定过程中通常不会费心标准化肺的充气,分析往往基于一个相当主观的评分系统。虽然这有时可能足以对肺肿瘤的大小进行大致估计,但对肺结构或细胞进行任何适当的立体定量分析都需要可重复的固定程序和随后的肺体积测量。在这里,我们描述了在压力下固定肺部以及随后准确测量固定肺体积的简单可靠程序。唯一的要求是一台在1毫克至300克范围内准确的实验室天平。因此,本文介绍的程序可以大大提高在小鼠中创建、治疗和分析肺癌的能力。