Tu Haohua, Liu Yuan, Turchinovich Dmitry, Marjanovic Marina, Lyngsø Jens, Lægsgaard Jesper, Chaney Eric J, Zhao Youbo, You Sixian, Wilson William L, Xu Bingwei, Dantus Marcos, Boppart Stephen A
Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA, Max Planck Institute for Polymer Research, Ackermannweg 10, Mainz, 55128, Germany.
Nat Photonics. 2016 Aug;10(8):534-540. doi: 10.1038/nphoton.2016.94. Epub 2016 May 23.
The preparation, staining, visualization, and interpretation of histological images of tissue is well-accepted as the gold standard process for the diagnosis of disease. These methods were developed historically, and are used ubiquitously in pathology, despite being highly time and labor intensive. Here we introduce a unique optical imaging platform and methodology for label-free multimodal multiphoton microscopy that uses a novel photonic crystal fiber source to generate tailored chemical contrast based on programmable supercontinuum pulses. We demonstrate collection of optical signatures of the tumor microenvironment, including evidence of mesoscopic biological organization, tumor cell migration, and (lymph-)angiogenesis collected directly from fresh mammary tissue. Acquisition of these optical signatures and other cellular or extracellular features, which are largely absent from histologically processed and stained tissue, combined with an adaptable platform for optical alignment-free programmable-contrast imaging, offers the potential to translate stain-free molecular histopathology into routine clinical use.
组织的组织学图像的制备、染色、可视化和解读,作为疾病诊断的金标准流程已被广泛接受。这些方法是历史上发展起来的,尽管耗时且费力,但在病理学中被广泛使用。在此,我们介绍一种独特的光学成像平台和无标记多模态多光子显微镜方法,该方法使用新型光子晶体光纤源,基于可编程超连续脉冲生成定制的化学对比度。我们展示了从新鲜乳腺组织直接收集肿瘤微环境的光学特征,包括介观生物组织、肿瘤细胞迁移和(淋巴)血管生成的证据。获取这些光学特征以及其他细胞或细胞外特征(这些在组织学处理和染色的组织中基本不存在),再结合用于无光学对准可编程对比度成像的适应性平台,为将无染色分子组织病理学转化为常规临床应用提供了潜力。