Caballero Montserrat, Lightfoot Harry M, Lapaglia Michael, Pleasant Andrew, Hatada Seigo, Cairns Bruce A, Fair Jeffrey H
Department of Surgery, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7211, USA.
J Surg Res. 2007 Aug;141(2):134-40. doi: 10.1016/j.jss.2006.04.041. Epub 2007 May 31.
Embryonic stem (ES) cells have been investigated as a potential replacement therapy for failed organs, such as the liver. However, detection of hepatic engraftment from candidate stem cells has been difficult due to low engraftment efficiency. Previous detection methods required that the graft be processed by molecular and/or immunohistochemical techniques, limiting further functional studies. This study evaluated the use of three-dimensional fluorescent stereomicroscopy for gross detection of ES cell derived hepatic engraftment.
Murine ES cells expressing the enhanced green fluorescence protein (EGFP) underwent directed endodermal lineage differentiation. Three days after two thirds partial hepatectomy, cells were injected into the liver parenchyma, and livers were harvested at 10 to 20 d and examined by fluorescence stereomicroscopy with a GFP2 long pass filter (100447084; Leica Microsystems AG, Wetzlar, Germany). The sensitivity and reliability of the test was evaluated using quantitative polymerase chain reaction (q-PCR) to assay for the presence of EGFP mRNA in the tissue.
Fluorescent microscopy detected EGFP-positive cells engrafted with normal histology in 5 of 11 specimens. EGFP mRNA was confirmed in all five specimens by q-PCR. Only one of the 11 specimens was negative by fluorescence stereomicroscopy and positive by q-PCR, P < 0.02, Fisher's exact test.
Utilization of three-dimensional stereomicroscopy with a GFP2 long pass filter is a powerful and fast screening tool for GFP-ES derived hepatic engraftment.
胚胎干细胞(ES细胞)已被研究作为诸如肝脏等衰竭器官的潜在替代疗法。然而,由于移植效率低,检测候选干细胞的肝移植一直很困难。以前的检测方法要求通过分子和/或免疫组织化学技术处理移植物,这限制了进一步的功能研究。本研究评估了三维荧光体视显微镜用于ES细胞源性肝移植大体检测的应用。
表达增强型绿色荧光蛋白(EGFP)的小鼠ES细胞进行定向内胚层谱系分化。在三分之二部分肝切除术后三天,将细胞注入肝实质,在10至20天收获肝脏,并使用GFP2长通滤光片(100447084;徕卡微系统公司,德国韦茨拉尔)通过荧光体视显微镜检查。使用定量聚合酶链反应(q-PCR)检测组织中EGFP mRNA的存在,评估该检测的敏感性和可靠性。
荧光显微镜在11个标本中的5个中检测到具有正常组织学的EGFP阳性细胞移植。通过q-PCR在所有五个标本中均证实了EGFP mRNA。11个标本中只有1个通过荧光体视显微镜检查为阴性,通过q-PCR检查为阳性,P<0.02,Fisher精确检验。
使用带有GFP2长通滤光片的三维体视显微镜是用于GFP-ES源性肝移植的强大而快速的筛选工具。