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Autofluorescence multiphoton microscopy for visualization of tissue morphology and cellular dynamics in murine and human airways

机译:自发荧光多光子显微镜用于观察鼠和人气道的组织形态和细胞动力学

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The basic understanding of inflammatory airway diseases greatly benefits from imaging the cellular dynamics of immune cells. Current imaging approaches focus on labeling specific cells to follow their dynamics but fail to visualize the surrounding tissue. To overcome this problem, we evaluated autofluorescence multiphoton microscopy for following the motion and interaction of cells in the airways in the context of tissue morphology. Freshly isolated murine tracheae from healthy mice and mice with experimental allergic airway inflammation were examined by autofluorescence multiphoton microscopy. In addition, fluorescently labeled ovalbumin and fluorophore-labeled antibodies were applied to visualize antigen uptake and to identify specific cell populations, respectively. The trachea in living mice was imaged to verify that the ex vivo preparation reflects the in vivo situation. Autofluorescence multiphoton microscopy was also tested to examine human tissue from patients in short-term tissue culture. Using autofluorescence, the epithelium, underlying cells, and fibers of the connective tissue, as well as blood vessels, were identified in isolated tracheae. Similar structures were visualized in living mice and in the human airway tissue. In explanted murine airways, mobile cells were localized within the tissue and we could follow their migration, interactions between individual cells, and their phagocytic activity. During allergic airway inflammation, increased number of eosinophil and neutrophil granulocytes were detected that moved within the connective tissue and immediately below the epithelium without damaging the epithelial cells or connective tissues. Contacts between granulocytes were transient lasting 3?min on average. Unexpectedly, prolonged interactions between granulocytes and antigen-uptaking cells were observed lasting for an average of 13?min. Our results indicate that autofluorescence-based imaging can detect previously unknown immune cell interactions in the airways. The method also holds the potential to be used during diagnostic procedures in humans if integrated into a bronchoscope.
机译:对炎症性气道疾病的基本了解极大地受益于对免疫细胞的细胞动力学成像。当前的成像方法集中于标记特定的细胞以跟随它们的动态,但是不能可视化周围的组织。为了克服这个问题,我们评估了自发荧光多光子显微镜在组织形态学背景下跟踪气道中细胞的运动和相互作用的能力。通过自体荧光多光子显微镜检查从健康小鼠和患有实验性过敏性气道炎症的小鼠中新鲜分离的鼠气管。此外,分别使用荧光标记的卵清蛋白和荧光团标记的抗体观察抗原摄取并鉴定特定的细胞群。对活体小鼠的气管成像,以验证离体制剂反映了体内情况。还测试了自发荧光多光子显微镜,以检查来自短期组织培养中患者的人体组织。使用自发荧光,在分离的气管中鉴定出结缔组织的上皮,下层细胞和纤维以及血管。在活体小鼠和人类气道组织中可以看到类似的结构。在外植鼠气道中,活动细胞位于组织内,我们可以追踪它们的迁移,单个细胞之间的相互作用以及它们的吞噬活性。在过敏性气道炎症期间,检测到嗜酸性粒细胞和嗜中性粒细胞增多,这些嗜酸性粒细胞和嗜中性粒细胞在结缔组织内移动并直接位于上皮细胞下方,而不会损害上皮细胞或结缔组织。粒细胞之间的接触是短暂的,平均持续3分钟。出乎意料的是,观察到粒细胞与抗原摄取细胞之间的相互作用延长了,平均持续了13分钟。我们的结果表明,基于自身荧光的成像可以检测出气道中以前未知的免疫细胞相互作用。如果集成到支气管镜中,该方法还具有在人类诊断过程中使用的潜力。

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