From the Departments of Laboratory Medicine (Dr Torres) and Neurology (Dr Levene), Yale University School of Medicine, New Haven, Connecticut; and the Department of Biomedical Engineering, Yale University School of Engineering and Applied Science, New Haven, Connecticut (Drs Torres and Levene and Mr Vesuna).
Arch Pathol Lab Med. 2014 Mar;138(3):395-402. doi: 10.5858/arpa.2013-0094-OA. Epub 2013 Jul 5.
Despite continuing advances in tissue processing automation, traditional embedding, cutting, and staining methods limit our ability for rapid, comprehensive visual examination. These limitations are particularly relevant to biopsies for which immediate therapeutic decisions are most necessary, faster feedback to the patient is desired, and preservation of tissue for ancillary studies is most important. The recent development of improved tissue clearing techniques has made it possible to consider use of multiphoton microscopy (MPM) tools in clinical settings, which could address difficulties of established methods.
To demonstrate the potential of MPM of cleared tissue for the evaluation of unembedded and uncut pathology samples.
Human prostate, liver, breast, and kidney specimens were fixed and dehydrated by using traditional histologic techniques, with or without incorporation of nucleic acid fluorescent stains into dehydration steps. A benzyl alcohol/benzyl benzoate clearing protocol was substituted for xylene. Multiphoton microscopy was performed on a home-built system.
Excellent morphologic detail was achievable with MPM at depths greater than 500 μm. Pseudocoloring produced images analogous to hematoxylin-eosin-stained images. Concurrent second-harmonic generation detection allowed mapping of collagen. Subsequent traditional section staining with hematoxylin-eosin did not reveal any detrimental morphologic effects. Sample immunostains on renal tissue showed preservation of normal reactivity. Complete reconstructions of 1-mm cubic samples elucidated 3-dimensional architectural organization.
Multiphoton microscopy on cleared, unembedded, uncut biopsy specimens shows potential as a practical clinical tool with significant advantages over traditional histology while maintaining compatibility with gold standard techniques. Further investigation to address remaining implementation barriers is warranted.
尽管组织处理自动化技术不断取得进展,但传统的包埋、切割和染色方法限制了我们进行快速、全面的可视化检查的能力。这些限制在需要立即做出治疗决策的活检中尤为重要,因为我们希望更快地向患者提供反馈,并且最重要的是要保留组织用于辅助研究。最近改进的组织透明化技术的发展使得在临床环境中考虑使用多光子显微镜 (MPM) 工具成为可能,这可以解决现有方法的困难。
展示 MPM 对未包埋和未切割的病理样本进行评估的潜力。
人类前列腺、肝脏、乳房和肾脏标本使用传统的组织学技术进行固定和脱水,其中包括或不包括将核酸荧光染料纳入脱水步骤。用苯甲醇/苯甲酸苄酯透明液代替二甲苯。多光子显微镜在自制系统上进行。
MPM 可在大于 500μm 的深度实现出色的形态细节。伪彩色产生类似于苏木精-伊红染色图像的图像。同时进行的二次谐波产生检测允许对胶原进行映射。随后用苏木精-伊红进行传统的切片染色不会显示出任何形态学的有害影响。对肾脏组织进行免疫染色的样本显示出正常反应性的保留。对 1mm 立方样本的完整重建阐明了三维结构组织。
对未包埋、未切割的活检标本进行多光子显微镜检查显示出作为一种实用的临床工具的潜力,与传统组织学相比具有显著优势,同时保持与金标准技术的兼容性。需要进一步调查以解决剩余的实施障碍。