Freezing of rat macrophages

The effect of freeze-thawing was studied in cryoprotected (10% dimethyl sulfoxide) rat peritoneal macrophages. Recovery after post-thaw washing was about 50%. Phagocytosis of latex particles seemed unhampered by this procedure, whereas the abilty to adhere to glass and the amount of Fc and C₃ receptors were moderately reduced. Low temperature preservation of macrophages might be a useful storage method, as it is for lymphocytes and tissue culture cells.     

大熊猫精液超低温冷冻的比较

对卧龙自然保护区大熊猫研究中心的9只雄性大熊猫电刺激采精,比较研究了稀释液中甘油含量、精液离心、不同稀释液和冷冻方法对大熊猫精液超低温冷冻保存后的活力、运动状态和顶体的影响。稀释液中甘油的含量为4％－5％较好,冻精解冻后的活力和顶体的正常率能保持鲜精的一半。离心和未离心的精液经超低温冷冻,解冻后的活力和运动状态都较接近。TEST和SFS两种稀释液的效果没有明显的差异。细管的冷冻过程较颗粒方便、快捷,时间容易控制,是一种较好的超低温冷冻精液的方法。     

Freezing human ES cells

Here we demonstrate how our lab freezes HuES human embryonic stem cell lines. A healthy, exponentially expanding culture is washed with PBS to remove residual media that could otherwise quench the Trypsin reaction. Warmed 0.05% Trypsin-EDTA is then added to cover the cells, and the plate allowed to incubate for up to 5 mins at room temperature. During this time cells can be observed rounding, and colonies lifting off the plate surface. Gentle repeated pipetting will remove cells and colonies from the plate surface. Trypsinized cells are placed in a standard conical tube containing pre-warmed hES cell media to quench remaining trypsin, and then spun. Cells are resuspended growth media at a concentration of approximately one million cells in one mL of media, a concentration such that one frozen aliquot is sufficient to resurrect a culture on a 10 cm plate. After cells are adequately resuspended, ice cold freezing media is added at equal volume. Cell suspensions are mixed thoroughly, aliquoted into freezing vials, and allowed to slowly freeze to -80 C over 24 hours. Frozen cells can then moved to the vapor phase of liquid nitrogen for long term storage, or remain at -80 for approximately six months.     

Plant Freezing and Damage

Imaging methods are giving new insights into plant freezingand the consequent damage that affects survival and distributionof both wild and crop plants. Ice can enter plants through stomataand hydathodes. Intrinsic nucleation of freezing can also occur.The initial growth of ice through the plant can be as rapidas 40 mm s^-1, although barriers can limit this growth. Onlya small fraction of plant water is changed to ice in this firstfreezing event. Nevertheless, this first rapid growth of iceis of key importance because it can initiate further, potentiallylethal, freezing at any site that it reaches. Some organs andtissues avoid freezing by supercooling. However, supercooledparts of buds can dehydrate progressively, indicating that avoidanceof freezing-induced dehydration by deep supercooling is onlypartial. Extracellular ice forms in freezing-intolerant as wellas freezing-tolerant species and causes cellular dehydration.The single most important cause of freezing-damage is when thisdehydration exceeds what cells can tolerate. In freezing-adaptedspecies, lethal freezing-induced dehydration causes damage tocell membranes. In specific cases, other factors may also causedamage, examples being cell death when limits to deep supercoolingare exceeded, and death of shoots when freezing-induced embolismsin xylem vessels persist. Extracellular masses of ice can damagethe structure of organs but this may be tolerated, as in extra-organfreezing of buds. Experiments to genetically engineer expressionof fish antifreeze proteins have not improved freezing toleranceof sensitive species. A better strategy may be to confer toleranceof cellular dehydration.Copyright 2001 Annals of Botany Company Freezing, dehydration, infrared video thermography, low temperature scanning electron microscopy, NMR micro-imaging     

Freezing material without electricity

When collecting in the field, biological samples can be kept cool at 0 C in ice slush, or frozen at -20 C in a crushed ice + salt (NaCl) cold mixture, in well-insulated containers, for several hours or days.     

Freezing injury to erythrocytes. I. Freezing patterns and post-thaw hemolysis.

The extent of hemolysis of human red blood cells suspended in different concentrations of glycerol and frozen at various cooling rates was investigated on the basis of morphological observation in the frozen state. Hemolysis of the cells in the absence of glycerol showed a V-shaped curve in terms of cooling rates. There was 70% hemolysis at an optimal cooling rate of approximately 10³ °C/min and 100% hemolysis at all other rates tested. Morphologically, a lower than optimal cooling rate resulted in cellular shrinkage, while a higher than optimal rate resulted in the formation of intracellular ice.The cryoprotective effect of glycerol was dependent upon its concentration and on the cooling rate. Samples frozen at 10³ and 10⁴ °C/min showed freezing patterns which differed from cell to cell. The size of intraand extracellular ice particles became smaller, and there was less shrinkage or deformation of cells as the rate of cooling and concentration of glycerol were increased.There was some correlation between the morphology of frozen cells and the extent of post-thaw hemolysis, but the minimum size of intracellular ice crystals which might cause hemolysis could not be estimated. As a cryotechnique for electron microscopy, the addition of 30% glycerol and ultrarapid freezing at 10⁵ °C/min are minimum requirements for the inhibition of ice formation and the prevention of the corresponding artifacts in erythrocytes.     

Freezing Tolerance of Shoot and Flower Primordia of Coniferous Buds by Extraorgan Freezing

Shoot and flower primordia of vegetative and flower buds ofextremely or very hardy conifers belonging to the subfamilyAbietoideae of the Pinaceae, survived between –40 and–70?C by extraorgan freezing, which differed greatly dependingupon species. The water in these organs gradually froze outwith decreasing temperatures when cooled very slowly, whichenabled these organs to survive %40?C or below. The same icesegregation in shoot and flower primordia by extraorgan freezingwas observed in most of the temperate conifers belonging toTaxaceae, Cephalotaxaceae, Taxodiaceae and Cuppressaceae, makingthem resistant to temperatures between –15 and –25?C.In these conifers, scales acted as an ice sink, unlike the conifersof Abietoideae. The rates of cooling and exosmosis of waterin the shoot or flower primordia, their size, and their abilityto tolerate freeze-dehydration or its related stress play animportant role in determining whether death is caused by freeze-dehydrationor intraorgan freezing. Even in very hardy conifers, low temperature exotherms fromfreezing within the shoot primordia appeared between –30and –35?C on the DTA profiles when cooled continuouslyunder laboratory conditions from 5?C to –50?C at 2 to5?C/h. Appearance of low temperature exotherms always resultedin death. However, in the coldest area of Hokkaido, where theair temperature cools down to –40?C or below nearly everyyear, such an intraorgan freezing seems seldom to occur, especiallyin natural stands. On the other hand, low temperatures below–25?C seldom occur in warm-temperate climates. Thus, itmay be considered that in both boreal and temperate coniferstheir shoot and flower primordia seem to tolerate freeze dehydrationby extraorgan freezing under natural conditions. ¹ Contribution No. 2431 from the rnstitute of Low TemperatureScience. (Received March 27, 1982; Accepted August 12, 1982)     

Freezing of stallion epididymal sperm

Inseminations with frozen-thawed epididymal sperm have resulted in low-pregnancy rates of mares. If fertility of epididymal sperm could be improved, it would help to preserve genetic material from stallions that have suffered severe injuries, been castrated or have died. The aim of the present study was to investigate the effect of different extenders and pre-freezing addition of capacitation media on freezability of epididymal sperm and on storage at 5 degrees C for 24h. In experiment 1, epididymal sperm samples were diluted and subsequently frozen with three different extenders: Botu-Crio, EDTA-Lactose and INRA-82. Motility analysis using computer assisted sperm analyzer (CASA) demonstrated better motility for sperm in Botu-Crio than in the other extenders; EDTA-Lactose yielded better motility than INRA-82 on most evaluated parameters. There was no difference in membrane integrity among the studied extenders. From 18 inseminated mares, 12 (66%) were pregnant 15 days after AI with frozen-thawed epididymal sperm showing that Botu-Crio was able to maintain the fertility potential. In experiment 2, the effect of incubation of epididymal sperm before freezing in three capacitation media (Fert Talp, Sperm Talp, Talp+Progesterone), seminal plasma, or control was tested. Based on post-thaw motility evaluation by CASA, samples incubated in Sperm Talp showed better motility values. There were no differences in plasma or acrosomal membranes or in mitochondrial potential among groups. We concluded that Botu-Crio was better than the other extenders in the ability to preserve epididymal sperm and that pre-freeze addition of Sperm Talp was also beneficial.     

高山植物的抗寒抗冻特性

综述了高山植物光合作用对冰冻低温胁迫的反应和适应特性,阐述了高山植物呼吸作用的低温适应特点;对高山植物抗冻机制作了详细分析和讨论。     

高山植物的抗寒抗冻特性

综述了高山植物光合作用对冰冻低温胁迫的反应和适应特性,阐述了高山植物呼吸作用的低温适应特点;对高山植物抗冻机制作了详细分析和讨论。     

Dichloro-tetrafluoro-ethane as a Freezing Agent

Surgical skin planing is, in the hands of an experienced operator, a safe and highly effective procedure for treating a number of cutaneous defects, most notably pitted acne scars.The operation is facilitated by the use of a new instrument (jet-spray handpiece) which allows the operator to freeze the skin and plane it almost simultaneously, and by a new freezing agent, dichlorotetrafluoro-ethane, which adds to the safety by eliminating the old hazards of inflammability, explosion, and the toxic inhalation of ethyl chloride.The ability to sharply differentiate between keloid and hypertrophic scar is fundamental to surgical skin planing. A hypertrophic scar results from the removal or destruction of the cutaneous appendages (hair follicles, oil and sweat glands and ducts); whereas a keloid is an idiosyncratic response without regard to damage of the appendages.Properly performed surgical planing does not entirely remove these appendages and therefore healing occurs without scarring.