Cell Preservation Technology最新文献

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Mammalian Cell Desiccation: Facing The Challenges 哺乳动物细胞干燥:面临挑战
Cell Preservation Technology Pub Date : 2006-12-01 DOI: 10.1089/CPT.2006.9996
Tamir Kanias, J. Acker
{"title":"Mammalian Cell Desiccation: Facing The Challenges","authors":"Tamir Kanias, J. Acker","doi":"10.1089/CPT.2006.9996","DOIUrl":"https://doi.org/10.1089/CPT.2006.9996","url":null,"abstract":"The current techniques for the biopreservation of mammalian cells, such as red blood cells, human platelets, sperm cells, and stem cells, rely on hypothermic storage, which has many disadvantages including high cost of maintenance and limited transportation ability. Preservation of biomaterial in the dry state at room temperature is a novel approach to meeting the growing demand for human mammalian cells in regenerative medicine. Presently, many proteins, bacteria, pharmaceutical drugs, and foods are successfully preserved in the dried state. However, mammalian cells are desiccation sensitive and cannot be stabilized in the dried state without the use of biotechnology. Several techniques have been developed to overcome this challenge including the introduction of sugars into the cells. To date there has been encouraging, but limited, success in the development of techniques for the desiccation and dry storage of human platelets and sperm cells. This review summarizes the current state of the preservation ...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"253-277"},"PeriodicalIF":0.0,"publicationDate":"2006-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.9996","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60915038","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 44
Embryonic Stem Cell Processing in Obtaining Insulin-Producing Cells: A Technical Review 胚胎干细胞加工获得胰岛素生成细胞:技术综述
Cell Preservation Technology Pub Date : 2006-12-01 DOI: 10.1089/CPT.2006.9997
R. Enseñat‐Waser, A. Santana, Beatriz Paredes, M. Zenke, J. Reig, E. Roche
{"title":"Embryonic Stem Cell Processing in Obtaining Insulin-Producing Cells: A Technical Review","authors":"R. Enseñat‐Waser, A. Santana, Beatriz Paredes, M. Zenke, J. Reig, E. Roche","doi":"10.1089/CPT.2006.9997","DOIUrl":"https://doi.org/10.1089/CPT.2006.9997","url":null,"abstract":"Diabetes mellitus derives from the absence of insulin hormone in the organism, usually due to the destruction of insulin-producing pancreatic β-cells either by immune attack or glucolipotoxic mechanisms. Insulin is a key hormone in controlling nutrient (glucose and fatty acids) homeostasis, as well as modulating both their uptake and metabolism by peripheral target tissues, such as skeletal muscle and adipose tissue. Insulin injection can partially mimic endogenous hormone function, although it does not avoid the appearance of secondary complications such as retinopathy, nephropathy, neuropathy, and cardiovascular disorders. Implantation of de novo insulin-producing cells in the organism could be a long-term solution in the treatment of the disease, restoring the lost function. Transplantation of highly pure isolated islets (pancreatic cell clusters where β-cells are located) from cadaveric donors is a possibility, although there are still many problems to resolve, such as immune rejection, low isolation ...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"278-289"},"PeriodicalIF":0.0,"publicationDate":"2006-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.9997","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60915105","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
In vitro culture of cryopreserved caprine ovarian tissue pieces and isolated follicles 超低温保存的山羊卵巢组织块和离体卵泡的体外培养
Cell Preservation Technology Pub Date : 2006-12-01 DOI: 10.1089/CPT.2006.9998
A. Rodrigues, S. Costa, Rita Santos, C. Amorim, C. M. Lucci, S. Báo, J. Nunes, D. Rondina, J. R. Figueiredo
{"title":"In vitro culture of cryopreserved caprine ovarian tissue pieces and isolated follicles","authors":"A. Rodrigues, S. Costa, Rita Santos, C. Amorim, C. M. Lucci, S. Báo, J. Nunes, D. Rondina, J. R. Figueiredo","doi":"10.1089/CPT.2006.9998","DOIUrl":"https://doi.org/10.1089/CPT.2006.9998","url":null,"abstract":"The objective of the present study was to evaluate the effects of cryopreservation of goat preantral follicles, in situ and isolated, using dimethyl sulfoxide (DMSO) and ethylene glycol (EG). Follicles were cryopreserved and cultured in vitro, and follicle viability was assessed by Trypan Blue staining before and after culture. The viability of follicles cryopreserved in situ using 1.5 M DMSO (64% ± 5.3 and 60% ± 7.4) or 3.0 M EG (58% ± 3.7 and 45% ± 4.4) after days 1 and 5, respectively, of culture was lower (p 0.05). For isolated follicles, the percentage of viable fresh follicles was higher than follicles cryopreserved in EG on days 1 and 5 of culture, and in DMSO on day 1 of culture. Follicle diameter was not altered during culture, both for fresh and cryopreserved follicles and when follicles were cultured in situ or isolated. In conclusion, caprine preantral follicles were successfully cryopreserved, especially in situ, and follicle viability after isolation was similar between fresh and cryopreserved follicles after 1 day of culture, when DMSO was used. © Mary Ann Liebert, Inc.","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"290-298"},"PeriodicalIF":0.0,"publicationDate":"2006-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.9998","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60915187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
Effect of Quercetin on Capacitation Status and Lipid Peroxidation of Stallion Spermatozoa 槲皮素对种马精子获能状态及脂质过氧化的影响
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.169
M. Mcniven, G. Richardson
{"title":"Effect of Quercetin on Capacitation Status and Lipid Peroxidation of Stallion Spermatozoa","authors":"M. Mcniven, G. Richardson","doi":"10.1089/CPT.2006.4.169","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.169","url":null,"abstract":"Lower fertility of preserved stallion semen may be caused by damage to the spermatozoa or premature capacitation during storage. We investigated the use of the flavonoid, quercetin, with a standard skim milk extender for storage of stallion spermatozoa to prevent premature capacitation and acrosome reaction and to reduce the damage to spermatozoa from lipid peroxidation. Several concentrations of quercetin (0.05, 0.1, 0.2, 0.3 mM) were mixed with skim milk-glucose extender, and the antioxidant effectiveness was assessed using xanthine–xanthine oxidase challenge for 21 h. The effect of quercetin on capacitation status of sperm was assessed during a 4 h incubation at 33°C, and a storage trial at 5°C for 6 days. In addition, the ability of sperm stored in quercetin extender to undergo capacitation and acrosome reaction was assessed using heparin and A23187. Lipid peroxidation in the sperm after challenge was inhibited by any concentration of quercetin in the medium, while 0.1 and 0.3 mM quercetin were most e...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"169-177"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.169","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60913456","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
The Field of Cellular Cryopreservation 细胞冷冻保存领域
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.147
J. Baust
{"title":"The Field of Cellular Cryopreservation","authors":"J. Baust","doi":"10.1089/CPT.2006.4.147","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.147","url":null,"abstract":"","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"147-148"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.147","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60912798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Osmotic Stress and Cryoprotectant Toxicity on Mouse Oocyte Fertilization and Subsequent Embryonic Development In Vitro 渗透应激和冷冻保护剂毒性对小鼠卵母细胞体外受精和胚胎发育的影响
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.149
J. Huang, Haixiao Chen, Seang Tan, R. Chian
{"title":"Effects of Osmotic Stress and Cryoprotectant Toxicity on Mouse Oocyte Fertilization and Subsequent Embryonic Development In Vitro","authors":"J. Huang, Haixiao Chen, Seang Tan, R. Chian","doi":"10.1089/CPT.2006.4.149","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.149","url":null,"abstract":"Supplementation of cryoprotectant agent (CPA) into freezing solution causes osmotic change and this change together with toxicity of CPA may damage the oocytes before freezing. The objectives of the present study were to evaluate the tolerance of mouse oocytes to osmotic changes and to compare the toxicity of the permeable CPAs. Denuded mouse oocytes were exposed to (1) 0.5 M, 1.0 M, or 2.0 M sucrose in HEPES-buffered modified human tubal fluid (mHTF), respectively, for 3 min at the room temperature; exposed to (2) either 1.0 M or 2.0 M ethylene glycol (EG), 1,2-propanediol (PROH), dimethyl sulfoxide (Me2SO) and glycerol in HEPES-buffered mHTF for 3 min at room temperature, respectively. Following exposure, the oocytes were inseminated by in vitro fertilization (IVF), and the zygotes were further cultured to assess embryonic development in vitro. Additional analyses included morphologic evaluation of meiotic spindle organization and chromosome alignment as well as aneuploidy. Exposure to 2.0 M sucrose sig...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"31 1","pages":"149-160"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.149","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60912820","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 29
Thermally Induced Introduction of Trehalose into Primary Rat Hepatocytes 热诱导海藻糖导入原代大鼠肝细胞
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.178
Xiaoming He, Arthi A. Amin, A. Fowler, M. Toner
{"title":"Thermally Induced Introduction of Trehalose into Primary Rat Hepatocytes","authors":"Xiaoming He, Arthi A. Amin, A. Fowler, M. Toner","doi":"10.1089/CPT.2006.4.178","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.178","url":null,"abstract":"Trehalose was introduced into suspended primary rat hepatocytes through pathways resulting from thermally induced alterations of the cellular membrane. The hepatocytes were suspended in a diluted hepatocyte culture medium (medium:dH2O = 1:2) with 0.4 M trehalose during thermal treatments. A significant amount of cytoplasmic trehalose (0.07 M) was detected using high-performance liquid chromatography (HPLC) after heating hepatocytes to 39°C for 10 min in trehalose-supplemented medium. High cell viability (approximately 90%) was retained. The cytoplasmic trehalose concentration reached a plateau (approximately 0.16 M) after heating for 1–2 h. However, the cell viability decreased significantly after 30 min of heating (< approximately 72%). It was further found that by repetitive heating between 0°C and 39°C every 10 min for 1 h (0–39°C, 1 h), high cell viability (approximately 83%) could be maintained and a high cytoplasmic trehalose concentration (approximately 0.13 M) could be obtained. The trehalose-lade...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"8 1","pages":"178-187"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.178","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60913606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 22
Permeability Characteristics of Ovine Primordial Follicles Calculated with Two Parameter Kedem-Katchalsky Formulation 用双参数Kedem-Katchalsky公式计算绵羊原始卵泡的渗透性
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.188
R. Devireddy, C. Amorim, S. Leibo
{"title":"Permeability Characteristics of Ovine Primordial Follicles Calculated with Two Parameter Kedem-Katchalsky Formulation","authors":"R. Devireddy, C. Amorim, S. Leibo","doi":"10.1089/CPT.2006.4.188","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.188","url":null,"abstract":"The osmotic responses of isolated ovine primordial follicles when suspended in various concentrations of several cryoprotective additives (CPAs) have recently been published. We have used the Kedem-Katchalsky formulation, written with two parameters as variables, to calculate permeability of the follicle membrane to water, Lp, and permeability to CPAs, ω. By fitting the model to the osmotic responses of follicles determined by Amorim and colleagues, we were able to calculate the permeability coefficients in the presence of 0.5, 1.0, 1.5, 2.0, or 2.5 M solutions of each of the following CPAs: dimethylsulfoxide (DMSO), ethylene glycol (EG), propylene glycol (PROH), and glycerol (GLY). In the presence of DMSO, the best-fit values of L p ranged from 0.15 to 0.29 × 10-14 m 3/N-sec, and ω ranged from 0.30 to 0.50 × 10 -11 mol/N-sec. In the presence of EG, the corresponding values of Lp ranged from 0.25 to 0.47 × 10-14 m 3/N-sec, and ω ranged from 0.20 to 0.65 × 10 -11 mol/N-sec. In the presence of PROH, Lp ranged from 0.10 to 0.62 × 10-14 m3/N-sec, and ω ranged from 0.10 to 0.40 × 10-11 mol/N-sec. And finally, in the presence of GLY, the best-fit values of Lp ranged from 0.19 to 0.32 × 10-14 m3/N-sec, and ω ranged from 0.05 to 0.32 × 10-11 mol/N-sec. The cross correlation or the reflection coefficient, σ, defined as σ = 1 - ωυCPA/ Lp, where υCPA is the partial mole volume of the CPA, ranged from 0.763 to 0.926 in the presence of DMSO, from 0.870 to 0.977 in the presence of EG, from 0.813 to 0.983 in the presence of PROH, and from 0.918 to 0.988 in the presence of GLY. These values of Lp and ω (and σ) can be used to predict the volumetric response of ovine follicles under arbitrary CPA loading and unloading conditions and consequently, the presumptive optimal conditions. © Mary Ann Liebert, Inc.","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"188-198"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.188","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60913703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
The Therapeutic Use of Cord Blood 脐带血的治疗用途
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.161
W. Arcese, A. Picardi, R. Cerretti, L. Cudillo, G. Angelis, L. Franceschini, L. Felice, M. Postorino
{"title":"The Therapeutic Use of Cord Blood","authors":"W. Arcese, A. Picardi, R. Cerretti, L. Cudillo, G. Angelis, L. Franceschini, L. Felice, M. Postorino","doi":"10.1089/CPT.2006.4.161","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.161","url":null,"abstract":"","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"161-168"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.161","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60912889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
A New Protection Solution for Freezing Small Numbers of Sperm Inside Empty Zona Pellucida: Osmangazi-Turk Solution 空透明带内冷冻少量精子的新保护液:Osmangazi-Turk溶液
Cell Preservation Technology Pub Date : 2006-11-17 DOI: 10.1089/CPT.2006.4.199
H. Hassa, Firdevs Gurer Dr., A. Yildirim, Cavit Can, V. Sahinturk, B. Tekin
{"title":"A New Protection Solution for Freezing Small Numbers of Sperm Inside Empty Zona Pellucida: Osmangazi-Turk Solution","authors":"H. Hassa, Firdevs Gurer Dr., A. Yildirim, Cavit Can, V. Sahinturk, B. Tekin","doi":"10.1089/CPT.2006.4.199","DOIUrl":"https://doi.org/10.1089/CPT.2006.4.199","url":null,"abstract":"It is well known that an effective freezing technique is crucial for small numbers of human sperm using empty zona pellucida as straws. However, this method still has problems. The goal of this stu...","PeriodicalId":51233,"journal":{"name":"Cell Preservation Technology","volume":"4 1","pages":"199-208"},"PeriodicalIF":0.0,"publicationDate":"2006-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1089/CPT.2006.4.199","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"60913246","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
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