John Elliot (2010) CIL:7874, Mus musculus, permanent cell line cell. CIL. Dataset

This is part of a triplicate data set of non-overlapping fields of NIH 3T3 fibroblasts cultured on polystyrene. Each set is indicated by the well number. Each image contains 4 images of each field as a time series. The first image is the phase contrast image. The second image channel is Tenascin-C promoter driven destabilized EGFP reporter vector. The third image is Texas Red C2-maleimide (to stain cell body), and the fourth image is Dapi (to stain nuclei).

Images were collected on a Zeiss Axiovert 100. The samples were viewed with a Zeiss A-plan 10x Ph1 0.25 NA objective and recorded with a CoolSnapFX camera using 2 x 2 binning. The filters were as follows: 1.) A custom dichroic multipass beam splitter optimized for imaging DAPI, EGFP and TxRed (part# BS51019+400dclp, Chroma Technology, VT); 2.) DAPI excitation filter-360/40 nm; 3.) DAPI emission filter-460/50 nm; 4.) EGFP excitation filter-470/40 nm; 5.) EGFP emission filter-525/50 nm; 6.) TxRed excitation filter-568/24 nm; 7.) TxRed emission filter-630/60 nm. Autofocus on the TxRed color channel was performed at each location before the series of images were collected.

Protocol: The cells were seeded on TCPS dishes at ~1000 cells/well during a passage cycle. The test cultures were incubated overnight before being rinsed with PBS and then fixed with 300 uM m-maleimidobenzoyl-N-hydroxysuccinimidyl ester (MBS) in microtubule stabilizing buffer (MTSB) composed of 4% (w/v) polyethylene glycol (PEG) 8000, 100 mM 1,4-piperazinediethanesulfonic acid (PIPES),10 mM ethylene glycol-bis(2-aminoethylether)-N,N,N’,N’-tetraacetic acid (EGTA), pH 6.9 for at least 16h at RT. The fixative was removed and solution of 0.05% Triton X100 in PBS containing 10 ng/mL of Tx Red C2-maleimide and 2 ng/mL DAPI for 2h. The staining solution was removed, cells were rinsed with PBS/3% BSA, and 0.05% sodium azide and PBS. A 50% glycerol/10 mM Tris, pH 8.0 containing 2ng/mL DAPI and 0.9g/l 1,4-diazobicyclo[2,2,2]octane (DABCO) as an antifade reagent was then added to each well for imaging purposes. The bottom of the wells were wiped with 70% ethanol wipe and then a dry wipe before imaging.

Purpose: The purpose of the dataset was to measure the distribution of EGFP fluorescence intensities within individual cells in the population. Using the image sets collected, a plugin for ImageJ was used to perform the following image analysis tasks. 1.) The Txred images (which is a general purpose cell body stain) were segmented by manual thresholding. 2.) The resulting mask was used to define cell ROIs on the DAPI and EGFP images. 3.) The number of nuclei in each ROI is determined from the DAPI image and the integrated intensity of the EGFP signal in the cell is determined from ROI in the EGFP image. 4.) A local background intensity around each cell in the EGFP image is determined by dilating the ROI by 3 pixels and determining the pixel intensities in only the 3 pixel dilation area. When this data is placed in a spread sheet, you can use the results to identify cell clusters (i.e. have more than 1 nuclei), debris or partial cell (i.e. no nuclei), poor EGFP/cell measurements (i.e. high background intensity). The spreadsheet can be used to measure the distribution of EGFP cell intensities within a population of cells. The phase images were collected as quality control and validation data. The phase images provide a human validation mechanism if there are questions about the staining and/or fluorescence detection in an image.

References: 1. Langenbach, K.J., Elliott, J.T., Tona, A., and Plant, A.L. (2006) Evaluating the correlation between fibroblast morphology and promoter activity on thin films of extracellular matrix proteins. BMC-Biotechnology 6(1):14. 2.Elliott, J.T., Halter, M., Woodward, J.T., Langenbach, K.J., Tona, A., Plant, A.L. (2008) Evaluating the performance of fibrillar collagen films formed at polystyrene surfaces as cell culture substrates. Biointerphases. 3(2):19-28.

此数据集为NIH 3T3成纤维细胞在聚苯乙烯上培养的非重叠区域之一。每个集合均以孔号标识。每张图像包含每个区域的4张图像，作为时间序列。首张图像为相衬图像。第二图像通道为Tenascin-C启动子驱动的去稳定EGFP报告基因载体。第三图像为Texas Red C2-马来酰亚胺（用于染色细胞体），第四图像为Dapi（用于染色细胞核）。图像采集于蔡司Axiovert 100显微镜。样品使用蔡司A-plan 10x Ph1 0.25 NA物镜观察，并通过CoolSnapFX相机以2 x 2合并的方式进行记录。使用的滤光片如下：1）用于成像DAPI、EGFP和TxRed的自定义二向色多路复用分束器（部件号BS51019+400dclp，Chroma Technology，VT）；2）DAPI激发滤光片-360/40 nm；3）DAPI发射滤光片-460/50 nm；4）EGFP激发滤光片-470/40 nm；5）EGFP发射滤光片-525/50 nm；6）TxRed激发滤光片-568/24 nm；7）TxRed发射滤光片-630/60 nm。在收集图像系列之前，对TxRed颜色通道进行自动对焦。实验方案：细胞在传代周期中以约1000个细胞/孔的密度接种于TCPS培养皿中。测试培养物过夜培养后，用PBS冲洗，然后用含有4%（w/v）聚乙二醇8000、100 mM 1,4-吡啶二乙烷磺酸（PIPES）、10 mM乙二醇双（2-氨基乙基）乙二酸（EGTA），pH 6.9的微管稳定缓冲液（MTSB）中的300 uM m-马来酰亚胺苯甲酰-N-羟基琥珀酰亚胺酯（MBS）固定至少16小时。去除固定剂后，用含有10 ng/mL的Tx Red C2-马来酰亚胺和2 ng/mL DAPI的0.05% Triton X100在PBS中的溶液固定2小时。去除染色溶液，细胞用PBS/3% BSA和0.05%叠氮化钠及PBS冲洗。然后向每个孔中加入含有2 ng/mL DAPI和0.9g/l 1,4-二氮杂双环[2,2,2]辛烷（DABCO）作为抗褪色剂的50%甘油/10 mM Tris，pH 8.0的溶液，以便进行成像。用70%乙醇擦拭孔底，然后进行干燥擦拭，再进行成像。目的：该数据集的目的是测量单个细胞群体中EGFP荧光强度的分布。利用收集到的图像集，使用ImageJ插件执行以下图像分析任务：1）对Txred图像（一种通用细胞体染色剂）进行手动阈值分割。2）使用得到的掩模在DAPI和EGFP图像上定义细胞感兴趣区域（ROI）。3）从DAPI图像中确定每个ROI中的核数，并从EGFP图像的ROI中确定细胞中EGFP信号的积分强度。4）通过将ROI膨胀3个像素，确定EGFP图像中每个细胞周围的局部背景强度。当将这些数据放置在电子表格中时，可以使用结果来识别细胞簇（即有超过1个核的细胞）、碎片或部分细胞（即无核），以及EGFP/细胞测量不良（即高背景强度）。电子表格可用于测量细胞群体中EGFP细胞强度的分布。相衬图像作为质量控制和数据验证而被收集。相衬图像提供了一种人工验证机制，以解决图像中染色和/或荧光检测的问题。参考文献：1. Langenbach, K.J.，Elliott, J.T.，Tona, A.，Plant, A.L.（2006）评估成纤维细胞形态与细胞外基质蛋白薄膜上启动子活性的相关性。BMC-Biotechnology 6(1):14。2.Elliott, J.T.，Halter, M.，Woodward, J.T.，Langenbach, K.J.，Tona, A.，Plant, A.L.（2008）评估在聚苯乙烯表面形成的纤维状胶原蛋白薄膜作为细胞培养基质的性能。Biointerphases. 3(2):19-28。