Dieter Brandner; Ginger Withers (2010) CIL:10348, Rattus, multipolar neuron. CIL. Dataset

Cultured hippocampal neurons after 14 days in vitro, immunostained for MAP2, a microtubule associated protein localized to dendrites (red) but not axons, which are not apparent in the immunofluorescence channel. Both axons, and dendrites, can be seen in the hidden phase micrograph which can be turned on using the edit function in the detailed viewer. Neurons at 10, 14, and 17 days in vitro are represented in this image group.

Detailed methods: Embryonic rat hippocampal neurons were prepared as previously described (see Kaech and Banker, 2006, Nat Protoc). Cells were prepared for fluorescent staining as previously described (Withers and Banker, 1998, in Culturing Nerve Cells, MIT Press). Briefly, cells were fixed (4% formaldehyde, 4% sucrose in phosphate buffered saline, pH 7.4), permeabilized with 0.25% Triton and immunostained for MAP2 (HM2, from Sigma with d549 conjugated secondary, excitation, 555, emission, 568, Jackson Immunoresearch). Images were acquired with a Leica DMRA microscope with a 40X lens (HCX PL Fluotar, NA 0.75), Photometrics CoolSnap ES CCD camera and MetaMorph software. A multilayer stack of the fluorescent image of MAP2 staining and the phase image was generated using MetaMorph.

在体外培养14天的海马神经元，经MAP2（微管相关蛋白，定位于树突，红色染色）免疫染色，轴突（在免疫荧光通道中不显影）未出现。在隐藏相位显微镜下，可通过详细查看器中的编辑功能激活，可观察到轴突和树突。本图像组展示了体外培养10天、14天和17天的神经元。详细方法：如前所述制备胚胎大鼠海马神经元（参见Kaech和Banker，2006，Nat Protoc）。细胞制备用于荧光染色，如前所述（Withers和Banker，1998，在《培养神经细胞》一书中，MIT Press）。简而言之，细胞经4%甲醛、4%蔗糖在磷酸盐缓冲盐溶液中固定（pH 7.4），用0.25%的Triton进行渗透，并经MAP2（HM2，Sigma产品，d549偶联二抗，激发波长555，发射波长568，Jackson Immunoresearch）进行免疫染色。图像采用Leica DMRA显微镜配备40X镜头（HCX PL Fluotar，NA 0.75），Photometrics CoolSnap ES CCD相机和MetaMorph软件获取。使用MetaMorph生成MAP2染色荧光图像和相位图像的多层堆栈。