Smith Sarah E, White Richard A, Grant David A, Grant Sheila A
Department of Bioengineering, University of Missouri, 250 Agricultural Engineering Building, Columbia, MO, 65211, USA.
Department of Orthopaedic Surgery, University of Missouri, Columbia, MO, 65212, USA.
Transgenic Res. 2015 Oct;24(5):911-9. doi: 10.1007/s11248-015-9891-7. Epub 2015 Jun 25.
Green fluorescent protein (GFP) animal models have become increasingly popular due to their potential to enhance in vivo imaging and their application to many fields of study. We have developed a technique to observe host tissue integration into scaffolds using GFP expressing swine and fluorescence imaging. Current fluorescence imaging preparation methods cannot be translated to a full GFP animal model due to several challenges and limitations that are investigated here. We have implanted tissue scaffolds into GFP expressing swine and have prepared explanted scaffolds for fluorescence imaging using four different methods including formalin fixation and paraffin embedding, vapor fixation, freshly prepared paraformaldehyde fixation, and fresh frozen tissue. Explanted scaffolds and tissue were imaged using confocal microscopy with spectral separation to evaluate the GFP animal model for visualization of host tissue integration into explanted scaffolds. All methods except fresh frozen tissue induced autofluorescence of the scaffold, preventing visualization of detail between host tissue and scaffold fibers. Fresh frozen tissue preparation allowed for the most reliable visualization of fluorescent host tissue integration into non-fluorescent scaffolds. It was concluded that fresh frozen tissue preparation is the best method for fluorescence imaging preparation when using scaffolds implanted into GFP whole animal models.
绿色荧光蛋白(GFP)动物模型因其在增强体内成像方面的潜力及其在许多研究领域的应用而越来越受欢迎。我们开发了一种利用表达GFP的猪和荧光成像来观察宿主组织整合到支架中的技术。由于本文所研究的几个挑战和限制,目前的荧光成像制备方法无法转化为完整的GFP动物模型。我们已将组织支架植入表达GFP的猪体内,并使用四种不同方法制备用于荧光成像的外植支架,包括福尔马林固定和石蜡包埋、蒸汽固定、新鲜制备的多聚甲醛固定以及新鲜冷冻组织。使用具有光谱分离功能的共聚焦显微镜对外植支架和组织进行成像,以评估GFP动物模型用于观察宿主组织整合到外植支架中的情况。除新鲜冷冻组织外,所有方法均诱导了支架的自发荧光,从而无法观察到宿主组织与支架纤维之间的细节。新鲜冷冻组织制备能够最可靠地观察到荧光宿主组织整合到非荧光支架中。得出的结论是,当使用植入GFP全动物模型的支架时,新鲜冷冻组织制备是荧光成像制备的最佳方法。