Jet freezing of cells and tissues with and without cryoprotectants

Author(s):  
M.V. Parthasarathy ◽  
Carole Daugherty ◽  
T. Müller

For the past several years cryofixation/freeze-substitution techniques have become valuable alternatives to chemical fixation of biological specimens. The superiority of cryofixation in preserving labile cell structures has been documented in several studies. Commercially available jet freezers and the BAL-TEC HPM010 high pressure freezer have extended high quality cryofixation from monolayer cells to cells relatively deep inside tissues. High pressure freezing can theoretically freeze biological materials of 0.5 mm thickness without the use of cryoprotectants and propane jet freezing is reported to freeze biological samples up to 40 μm in thickness without cryoprotection. Although high pressure freezing is the obvious method of choice for freezing large biological samples, its high cost combined with its apparent inability to consistently preserve microfilaments in some plant cells has prompted us to explore the capability of jet freezing to yield well frozen samples with and without cryoprotectants.We used the commercially available jet freezer JFD 030 (BAL-TEC) to obtain our results. Tightly pelleted cells sandwiched between 0.1 mm thick copper specimen carriers normally froze well without any cryoprotectants, after propane jet freezing (Figs. 1-2).

Author(s):  
J.Z. Kiss ◽  
L.A. Staehelin

Electron microscopy of chemically fixed plant tissues has lead to important insights into the relationship between structure and function of plant cells. However, the slow rate of chemical fixation (seconds to minutes) potentially permits numerous artifacts to be induced. Most of these limitations ofs chemical fixatives can be overcome by the use of cryofixation techniques since cell structure is stabilized rapidly (milliseconds). Several types of cryofixation techniques have been developed such as cold metal block freezing and propane jet freezing. Although application of these techniques has yielded exciting new information, they are limiting in that specimens can be preserved only to a relatively shallow depth (approx. 40 μm). In contrast, under optimal conditions, high pressure freezing (HPF) at 2100 bar can produce excellent freezing of biological samples up to 600 μm in thickness. Since a commercial HPF apparatus has only recently become available, the number of systematic structural studies of biological samples utilizing HPF is still rather limited, and basic questions concerning specimen preparation and processing, HPF artifacts, and interpretation of images need to be addressed.


2001 ◽  
Vol 7 (S2) ◽  
pp. 728-729
Author(s):  
Paul Walther

Imaging of fast frozen samples is the most direct approach for electron microscopy of biological specimen in a defined physiological state. It prevents chemical fixation and drying artifacts. High pressure freezing allows for ice-crystal-free cryo-fixation of tissue pieces up to a thickness of 200 urn and a diameter of 2 mm without prefixation. Such a frozen disc, however, is not directly amenable to electron microscopic observation: The structures of interest have to be made amenable to the electron beam, and the structures of interest must produce enough contrast to be recognized in the electron microscope. This can be achieved by freeze fracturing, cryo-sectioning or freeze substitution.The figures show high pressure frozen bakers yeast saccharomyces cerevisiae in the cryo-SEM (Figures 1 and 2) and after freeze substitution in the TEM (Figure 3). For high pressure freezing either a Bal-Tec HPM 010 (Princ. of Liechtenstein; Figures 1 and 2), or a Wohlwend HPF (Wohlwend GmbH, Sennwald, Switzerland; Figure 3) were used.


Author(s):  
LUCY RU-SIU YIN

The ultimate aim of ultrastructural fixation of biological specimen is to preserve all the compartments in their native state. Cryofixation is a superior method than conventional chemical fixation in reaching this goal. However, ice crystal formation during cryofixation often damages the structures. High pressure (2100 bar) freezing provides a way to alter freezing properties while cool down the specimen at a relatively high rate, minimizing the ice crystal formation. Nearly vitrified samples(up to 500 um) have been obtained with this method. Samples in suspension tend to get lost during high pressure freezing. The low percentage (∼30%) of successfully cryofixed specimens can be improved if the sample completely fills the cavity of the metal specimen carriers in which the specimen is frozen. Various methods to overcome sample loss are reported in this study.


2006 ◽  
Vol 12 (S02) ◽  
pp. 442-443
Author(s):  
DM Sherman ◽  
CP Huang

Extended abstract of a paper presented at Microscopy and Microanalysis 2006 in Chicago, Illinois, USA, July 30 – August 3, 2006


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