A novel flat-embedding method to prepare ultrathin cryosections from cultured cells in their in situ orientation

被引:39
作者
Oorschot, V
de Wit, H
Annaert, WG
Klumperman, J
机构
[1] Univ Utrecht, Med Ctr, Dept Cell Biol, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Inst Biomembranes, NL-3584 CX Utrecht, Netherlands
[3] Ctr Biomed Genet, Utrecht, Netherlands
[4] Katholieke Univ Leuven VIB, Gasthuisberg, Ctr Human Genet, Lab Neuronal Cell Biol, Louvain, Belgium
关键词
cryoultramicrotomy; immunogold; PC12; cells; hippocampal neurons; electron microscopy; flat-embedding;
D O I
10.1177/002215540205000809
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunogold labeling of ultrathin cryosections provides a sensitive and quantitative method to localize proteins at the ultrastructural level. An obligatory step in the routine preparation of cryosections from cultured cells is the detachment of cells from their substrate and subsequent pelleting. This procedure precludes visualization of cells in their in situ orientation and hampers the study of polarized cells. Here we describe a method to sample cultured cells from a petri dish or coverslip by embedding them in a 12% gelatin slab. Subsequently, sections can be prepared in parallel or perpendicular to the plane of growth. Our method extends the cryosectioning technique to applications in studying polarized cells and correlative light-electron microscopy.
引用
收藏
页码:1067 / 1080
页数:14
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