Department of Medical Informatics, School of Allied Health Sciences, Kitasato University, Sagamihara, Kanagawa, Japan.
Acta Histochem. 2012 Jul;114(4):318-26. doi: 10.1016/j.acthis.2011.06.008. Epub 2011 Jul 20.
Connexin 32s (Cx32s) were immunolocalized in fetal rat hepatocytes and their distribution was determined qualitatively. We used image analysis using a quantitative index (QI) of Cx32 (QI Cx32) defined as the area of Cx32s/number of cells in cultured fetal rat hepatocytes. Hepatocytes from livers of fetal rats were separated by collagenase digestion and low centrifugation on gestational day 17. Cells were cultured for 3 days in dexamethasone (DEX)-supplemented medium (Dex0). The medium was replaced with fresh medium and cells were continuously cultured for 3 days with DEX or epidermal growth factor supplemented medium (Dex3 or EGF3). After culture termination, cells were fixed and stained using the fluorescein-labeled antibody method for Cx32s and diaminophenylindole staining for nuclei. Thirty pairs of histological images for Cx32s and nuclei, 180 images in total, were obtained from each condition. The QI Cx32 significantly increased from 284.1 ± 102.0 (mean and SD, n=26) of Dex0 to 428.9 ± 101.0 of Dex3 (n=28) (P<0.05, Kruskal-Wallis test, then Steel-Dwass test). The increase of QI Cx32 was compatible with the morphological observations. The image analysis processing time after preparation for 180 images was reduced from 8h needed for manual operations to 1 min using ImageJ software with our macro routine.
缝隙连接蛋白 32 亚型(Cx32s)在胎鼠肝细胞中被免疫定位,并定性测定其分布。我们使用图像分析,采用一种量化指数(QI)来定义 Cx32(QI Cx32),该指数表示培养的胎鼠肝细胞中 Cx32 的面积/细胞数量。在妊娠第 17 天,通过胶原酶消化和低离心从胎鼠肝脏中分离肝细胞。细胞在添加地塞米松(DEX)的培养基(Dex0)中培养 3 天。将培养基更换为新鲜培养基,并在含有 DEX 或表皮生长因子的培养基中连续培养 3 天(Dex3 或 EGF3)。培养结束后,用荧光素标记的抗体法固定和染色 Cx32s,并用二氨基苯吲哚染色细胞核。每个条件获得 30 对 Cx32s 和细胞核的组织学图像,总共 180 个图像。QI Cx32 从 Dex0 的 284.1 ± 102.0(平均值和标准差,n=26)显著增加到 Dex3 的 428.9 ± 101.0(n=28)(P<0.05,Kruskal-Wallis 检验,然后 Steel-Dwass 检验)。QI Cx32 的增加与形态学观察结果一致。使用我们的宏程序,在准备 180 个图像后的图像分析处理时间从手动操作所需的 8 小时减少到 1 分钟。