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<i>In vitro</i>activity of cationic peptides against <i>Neisseria gonorrhoeae</i>and vaginal <i>Lactobacillus</i>species: The effect of divalent cations
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作者 Bernard J. Moncla Timothy A. Mietzner Sharon Louise Hillier 《Advances in Bioscience and Biotechnology》 2012年第3期249-255,共7页
One of the new strategies for the prevention of HIV acquisition is the use of microbicides such as topical microbicides including antimicrobial and antiviral peptides. Ideally, new drug candidates should kill pathogen... One of the new strategies for the prevention of HIV acquisition is the use of microbicides such as topical microbicides including antimicrobial and antiviral peptides. Ideally, new drug candidates should kill pathogens without determent to the normal bacterial flora considered important in health;such as hydrogen peroxide producing Lactobacillus species. The antimicrobial peptides LL-37 and LSA-5 were studied to determine their spectrum of activity against bacterial pathogens and normal flora organisms. The effects of divalent cations at biologically relevant concentrations were determined. We show the synthetic lytic peptide LSA-5 and the naturally occurring peptides LL-37 inactivate Neisseria gonorrhoeae but are less active against many normal flora members such as Lactobacillus species. Biologically relevant concentrations of calcium and magnesium prevented killing of sensitive strains. LSA-5 is more potent than LL-37, both are inhibited from killing sensitive strains by calcium and magnesium. Strains of Lactobacillus iners were killed by both microbicides even in the presence of the divalent cations. Antimicrobial peptides, such as LSA-5, have good potential for use in prevention of sexually transmitted disease, if formulated to sequester calcium and magnesium present in biological fluids. 展开更多
关键词 MICROBICIDES HIV LACTOBACILLUS Antimicrobial Peptides Cations Neisseria GONORRHOEAE
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Herpesvirus gene vectors and applications to human gene therapy 被引量:3
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作者 J.C.Gloriosc D.J.Fink 《中国实验血液学杂志》 CAS CSCD 1997年第3期283-283,共1页
Herpes simplex virus type 1 (HSV-1) naturallyestablishes latency in neurons of the nervous systemwith the concommitant expression of the latencyassociated transcripts (LATS) and the loss in
关键词 SIMPLEX TRANSCRIPTS latency promoter ATTEMPTED CITED IMMEDIATE deleted overcome aimed
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Identification and characterization of chondrogenic progenitor cells in the fascia of postnatal skeletal muscle
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作者 Guangheng Li Bo Zheng +4 位作者 Laura B.Meszaros Joseph B.Vella Arvydas Usas Tomoyuki Matsumoto Johnny Huard 《Journal of Molecular Cell Biology》 SCIE CAS CSCD 北大核心 2011年第6期369-377,共9页
Intramuscular injection of bone morphogenetic proteins(BMPs)has been shown to induce ectopic bone formation.A chondrogenic phase is typically observed in this process,which suggests that there may exist a chondrogenic... Intramuscular injection of bone morphogenetic proteins(BMPs)has been shown to induce ectopic bone formation.A chondrogenic phase is typically observed in this process,which suggests that there may exist a chondrogenic subpopulation of cells residing in skeletal muscle.Two prospective cell populations were isolated from rat skeletal muscle:fascia-derived cells(FDCs),extracted from gluteus maximus muscle fascia(epimysium)and muscle-derived cells(MDCs)isolated from the muscle body.Both populations were investigated for their cell surface marker profiles(flowcytometry analysis),proliferation rates as well as their myogenic and chondrogenic potentials.The majority of FDCs expressed mesenchymal stromal cell markers but not endothelial cell markers.FDCs underwent chondrogenic differentiation after BMP4 treatment in vitro,but not myogenic differentiation.Although MDCs showed chondrogenic potential,they expressed the myogenic cell marker desmin and readily underwent myogenic differentiation in vitro;however,the chondrogenic potential of the MDCs is confounded by the presence of FDC-like cells residing in the muscle perimysium and endomysium.To clarify the role of the muscle-derived myogenic cells in chondrogenesis,mixed pellets with varying ratios of FDCs and L6 myoblasts were formed and studied for chondrogenic potential.Our results indicated that the chondrogenic potential of the mixed pellets decreased with the increased ratio of myogenic cells to FDCs supporting the role of FDCs in chondrogenesis.Taken together,our results suggest that non-myogenic cells residing in the fascia of skeletal muscle have a strong chondrogenic potential and may represent a novel donor cell source for cartilage regeneration and repair. 展开更多
关键词 skeletal muscle FASCIA CHONDROCYTES CARTILAGE
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抗肌萎缩蛋白小基因对Duchenne肌营养不良病理改变的治疗作用 被引量:3
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作者 黎红华 张苏明 +5 位作者 方思羽 陈春莲 罗运达 官阳 汪道文 Xiao Xiao 《中华医学杂志》 CAS CSCD 北大核心 2003年第17期1513-1516,共4页
目的 探讨Duchenne肌营养不良 (DMD)的病理变化和治疗方法。方法 采用重组腺相关病毒载体 (rAAV)介导的人抗肌萎缩蛋白小基因 (SMCKA3999)观察DMD的病理改变和治疗作用。将抗肌萎缩蛋白小基因SMCKA3999克隆至rAAV并包装成rAAVSMCKA399... 目的 探讨Duchenne肌营养不良 (DMD)的病理变化和治疗方法。方法 采用重组腺相关病毒载体 (rAAV)介导的人抗肌萎缩蛋白小基因 (SMCKA3999)观察DMD的病理改变和治疗作用。将抗肌萎缩蛋白小基因SMCKA3999克隆至rAAV并包装成rAAVSMCKA3999病毒 ,将 5× 10 9病毒颗粒分多点注射于DMD模型鼠mdx腓肠肌 ,4个月后取局部肌组织 ,分别采用免疫荧光、埃文斯氏蓝染料、电镜等方法 ,观察rAAVSMCKA3999对DMD病理改变的治疗作用。结果 rAAVSMCKA3999有效稳定表达并使肌膜缺失的抗肌萎缩蛋白恢复 ,明显改善DMD肌肉病理改变。结论 rAAVSMCKA3999能显著改善mdx小鼠骨骼肌病理变化 。 展开更多
关键词 抗肌萎缩蛋白小基因 DUCHENNE肌营养不良 病理 治疗
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重组腺相关病毒载体介导的LacZ基因转染骨胳肌途径的研究 被引量:1
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作者 黎红华 张苏明 +3 位作者 方思羽 陈春莲 汪道文 Xiao Xiao 《中华医学遗传学杂志》 CAS CSCD 2004年第6期604-607,共4页
目的研究重组腺相关病毒载体(recombinantadeno-associatedvirusvector,rAAV)介导的β-半乳糖苷酶的结构基因LacZ,构建的rAAVLacZ病毒经不同途径给药后骨骼肌的转染效率、表达持续时间,为rAAV载体介导的目的基因对Duchenne肌营养不良的... 目的研究重组腺相关病毒载体(recombinantadeno-associatedvirusvector,rAAV)介导的β-半乳糖苷酶的结构基因LacZ,构建的rAAVLacZ病毒经不同途径给药后骨骼肌的转染效率、表达持续时间,为rAAV载体介导的目的基因对Duchenne肌营养不良的基因治疗探索合适的给药途径。方法采用报告基因LacZ、包装质粒PXX2、腺病毒成份辅助质粒PXX6三质粒共转染293细胞,包装重组腺相关病毒载体介导的rAAVLacZ,将rAAVLacZ局部腓肠肌肌肉注射转染至C57/BL6鼠骨胳肌,分别于单点注射后2个月、5个月取肌肉切片X-Gal染色。采用经股动脉注射rAAVLacZ观察LacZ基因在后肢骨骼肌的转染表达。结果(1)C57/BL6鼠局部肌注rAAVLacZ后,2个月和5个月时,均呈LacZ基因阳性表达,5个月时无表达减低。(2)经股动脉注射rAAVLacZ,C57/BL6小鼠后肢骨骼肌的肌膜及血管壁平滑肌LacZ基因广泛转染。结论重组腺相关病毒载体介导的报告基因LacZ可在C57/BL6鼠骨胳肌中高效持续表达5个月以上,经股动脉转染是有希望的下肢肌肉转染途径,此工作为神经肌肉遗传病,尤其是Duchenne肌营养不良基因治疗的进一步研究奠定了基础。 展开更多
关键词 重组腺相关病毒载体 转染 介导 LACZ基因 表达 骨骼肌 股动脉注射 报告基因 目的基因 质粒
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