Direct attachment of cell suspensions to high-pressure freezing specimen planchettes

被引:20
作者
Sawaguchi, A
Yao, X
Forte, JG
McDonald, KL [1 ]
机构
[1] Univ Calif Berkeley, Electron Microscopy Lab, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
来源
JOURNAL OF MICROSCOPY-OXFORD | 2003年 / 212卷
关键词
electron microscopy; freeze substitution; gastric parietal cell; HeLa cell; high-pressure freezing; immunogold labelling; primary culture;
D O I
10.1046/j.1365-2818.2003.01225.x
中图分类号
TH742 [显微镜];
学科分类号
摘要
We describe a procedure for high-pressure freezing (HPF) of cultured cells using the HPF aluminium planchettes as a substrate. Cells are either grown directly on planchettes covered with Matrigel or allowed to attach to poly-L-lysine-coated planchettes. This method allows for rapid transfer of the cells into the HPF and minimizes physical and physiological trauma to the cells. Furthermore, the yield of well-frozen cells approaches 100% for every cell type we have tried so far. In this report, we show well-preserved ultrastructure in mitotic and interphase HeLa cells, isolated gastric parietal cells and isolated gastric glands. Immunogold labelling of H+/K+-ATPase is shown in parietal cells of isolated gastric glands embedded in LR White resin. The aluminium planchettes appear to have little effect on cell physiology, as demonstrated by the fact that parietal cells cultured for 24-28 h on the planchettes retain their responsiveness to stimulation with histamine.
引用
收藏
页码:13 / 20
页数:8
相关论文
共 18 条
[1]   Syntaxin 3 is required for cAMP-induced acid secretion: streptolysin O-permeabilized gastric gland model [J].
Ammar, DA ;
Zhou, RH ;
Forte, JG ;
Yao, XB .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 282 (01) :G23-G33
[2]   Functionally distinct pools of actin in secretory cells [J].
Ammar, DA ;
Nguyen, PNB ;
Forte, JG .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 281 (02) :C407-C417
[3]  
Demaree RS, 2001, MICROWAVE TECHNIQUES AND PROTOCOLS, P1, DOI 10.1007/978-1-59259-128-2_1
[4]  
Duman JG, 2002, J CELL SCI, V115, P1251
[5]  
Forte JG, 1996, TRENDS CELL BIOL, V6, P45, DOI 10.1016/0962-8924(96)81009-9
[6]  
FORTE TM, 1977, GASTROENTEROLOGY, V73, P941
[7]   ADVANCES IN ULTRA-RAPID FREEZING FOR THE PRESERVATION OF CELLULAR ULTRASTRUCTURE [J].
GILKEY, JC ;
STAEHELIN, LA .
JOURNAL OF ELECTRON MICROSCOPY TECHNIQUE, 1986, 3 (02) :177-210
[8]   Cryopreparation provides new insight into the effects of brefeldin A on the structure of the HepG2 Gel apparatus [J].
Hess, MW ;
Müller, M ;
Debbage, PL ;
Vetterlein, M ;
Pavelkat, M .
JOURNAL OF STRUCTURAL BIOLOGY, 2000, 130 (01) :63-72
[9]  
Hohenberg H., 1997, Journal of Computer-Assisted Microscopy, V9, P69
[10]   HIGH-PRESSURE FREEZING OF CELL-SUSPENSIONS IN CELLULOSE CAPILLARY TUBES [J].
HOHENBERG, H ;
MANNWEILER, K ;
MULLER, M .
JOURNAL OF MICROSCOPY, 1994, 175 :34-43