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成骨细胞与诱导剂对骨髓基质干细胞的增殖与成骨分化的影响 被引量:10
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作者 黄开 章庆国 蔡国锋 《中国修复重建外科杂志》 CAS CSCD 北大核心 2006年第2期125-129,共5页
目的探索一种新的骨髓基质干细胞(marrowstromalstemcells,MSCs)增殖与成骨分化的体外诱导培养体系。方法乳大鼠颅骨来源的第3代成骨细胞与诱导剂(1nmol/L地塞米松、10mmol/Lβ-甘油磷酸钠、50μg/ml抗坏血酸)对大鼠股骨、胫骨来源的MSC... 目的探索一种新的骨髓基质干细胞(marrowstromalstemcells,MSCs)增殖与成骨分化的体外诱导培养体系。方法乳大鼠颅骨来源的第3代成骨细胞与诱导剂(1nmol/L地塞米松、10mmol/Lβ-甘油磷酸钠、50μg/ml抗坏血酸)对大鼠股骨、胫骨来源的MSCs生长的影响。于8块24孔板上培养MSCs,每孔接种5×104个第3代MSCs。按培养成分不同分为4组,每组2块。DMEM培养为对照组;诱导剂培养为诱导剂组;成骨细胞培养为成骨细胞组;联合使用成骨细胞与诱导剂培养为联合诱导组。计数诱导1~8d各组MSCs的数量并绘制细胞生长曲线,检测诱导10d的MSCs的碱性磷酸酶活性,采用RT-PCR检测诱导2周时MSCs骨钙素mRNA的表达水平。结果原代及传代MSCs形态正常。细胞生长曲线示MSCs数量均随时间延长增加。成骨细胞组增殖最快,诱导剂组增殖最慢,5~8d成骨细胞组及诱导剂组细胞数量与对照组比较,差异有统计学意义(P<0.05)。联合诱导组碱性磷酸酶活性为2.01±0.56U与对照组0.68±0.14U、诱导剂组1.27±0.43U及成骨细胞组0.77±0.19U比较,差异均有统计学意义(P<0.05)。对照组不表达骨钙素mRNA,诱导剂组为0.783±0.094、联合诱导组为0.814±0.071与成骨细胞组0.302±0.026比较,差异均有统计学意义(P<0.05)。结论联合使用成骨细胞和诱导剂诱导MSCs,不影响MSCs的正常增殖而促进MSCs的成骨分化,诱导效果较好,可望成为一种新的骨组织工程种子细胞的体外培养体系。 展开更多
关键词 骨组织工程 骨髓基质干细胞 成骨细胞 诱导剂培养
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Callus and Adventitious Buds Formation from Stem Explants of Balsam Pear (Momordica charantia L.) 被引量:2
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作者 Y. Tang L. Wang C. Ma B. Liu J. Liu H. X. Li 《Journal of Agricultural Science and Technology(B)》 2011年第1期146-150,共5页
The effects of sterilization pretreatment, sampling time and growth regulators on callus formation, explant contamination and adventitious bud induction from stems of balsam pear (Momordica charantia L.) were invest... The effects of sterilization pretreatment, sampling time and growth regulators on callus formation, explant contamination and adventitious bud induction from stems of balsam pear (Momordica charantia L.) were investigated. Sterilized for 6 rain with 0.1% (w/v) mercuric chloride solution is an essential sterilization method for stems. June and July proved to be better for material taking, followed by May. The callus formation rate of balsam pears reached the highest when medium added with IBA 1.0mg/L and BA 2.0 mg/L, while the optimum medium for adventitious bud induction was MS added with IBA 0.5mg/L and BA 4.0 mg/L. And it will provide theoretical and technical basis for rapid propagation and breeding. 展开更多
关键词 Balsam pear (Momordica charantia L.) tissue culture adventitious buds
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Conservation of Iris bismarckiana Regel (Iridaceae) Using Plant Regeneration via Somatic Embryogenesis
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作者 Sawsan A. Oran Ahmad H. AI-Gabbiesh 《Journal of Agricultural Science and Technology(A)》 2014年第7期605-611,共7页
In an attempt to propagate and conserve the rare, showy bulbous plants of Iris bismarckiana, newly recorded to the flora of Jordan and to contribute to the conservation the wild lris species in Jordan, a simple rapid,... In an attempt to propagate and conserve the rare, showy bulbous plants of Iris bismarckiana, newly recorded to the flora of Jordan and to contribute to the conservation the wild lris species in Jordan, a simple rapid, time consuming protocol has been developed using plant regeneration via somatic embryogenesis. Somatic embryogenesis was induced in zygotic embryo culture on Murashige and Skoog (MS) medium supplemented with 2,4-dichlorophenoxy acetic acid (8 mg/L) as the sole plant growth regulator, where both embryogenesis calli and somatic embryos were induced. Separation of embryos from embryo clusters was necessary to enhance the frequency of germination. Germination was stimulated by separation of embryos successfully from embryo clusters and transferred onto fresh MS medium. Data obtained were analyzed as a complete random design with three replications. Calli fragments that were transferred to embryogenesis induction medium (EIM) produced white embryo-like globular structures within two weeks. Within three more weeks, clusters of structures at various stages of development could be found on the same callus. The applied technique is rewarding and encouraging for further research on the endangered wild species of Iris in Jordan. 展开更多
关键词 CONSERVATION somatic embryogenesis plant regeneration flower base MS callus induction medium (CIM) Irisbismarckiana.
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Enhanced production of thermostable laccases from a native strain of Pycnoporus sanguineus using central composite design 被引量:1
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作者 Leticia I. RAMíREZ-CAVAZOS Charles JUNGHANNS +4 位作者 Rakesh NAIR Diana L. CáRDENAS-CHáVEZ Carlos HERNáNDEZ-LUNA Spiros N. AGATHOS Roberto PARRA 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2014年第4期343-352,共10页
The production of thermostable laccases from a native strain of the white-rot fungus Pycnoporus sanguineus isolated in Mexico was enhanced by testing different media and a combination of inducers including copper sulf... The production of thermostable laccases from a native strain of the white-rot fungus Pycnoporus sanguineus isolated in Mexico was enhanced by testing different media and a combination of inducers including copper sulfate(CuSO4).The best conditions obtained from screening experiments in shaken flasks using tomato juice,CuSO4,and soybean oil were integrated in an experimental design.Enhanced levels of tomato juice as the medium,CuSO4and soybean oil as inducers(36.8%(v/v),3 mmol/L,and 1%(v/v),respectively) were determined for 10 L stirred tank bioreactor runs.This combination resulted in laccase titer of 143000 IU/L(2,2'-azino-bis(3-ethylbenzthiazoline-6- sulfonic acid),pH 3.0),which represents the highest activity so far reported for P.sanguineus in a 10-L fermentor.Other interesting media resulting from the screening included glucose-bactopeptone which increased laccase activity up to 20000 IU/L,whereas the inducers Acid Blue 62 and Reactive Blue 19 enhanced enzyme production in this medium 10 times.Based on a partial characterization,the laccases of this strain are especially promising in terms of thermostability(half-life of 6.1 h at 60 °C) and activity titers. 展开更多
关键词 Enhanced laccase production Central composite design Screening media INDUCERS Tomato juice medium Soybean oil Copper sulfate
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