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21.
22.
Derivation and spontaneous differentiation of human embryonic stem cells 总被引:16,自引:0,他引:16 下载免费PDF全文
Embryonic stem (ES) cells are unique cells derived from the inner cell mass of the mammalian blastocyst. These cells are immortal and pluripotent, retain their developmental potential after prolonged culture, and can be continuously cultured in an undifferentiated state. Many in vitro differentiation systems have been developed for mouse ES cells, including reproducible methods for mouse ES cell differentiation into haematopoietic and neural precursors, cardiomyocytes, insulin‐secreting cells, endothelial cells and various other cell types. The derivation of new human ES cell lines provides the opportunity to develop unique models for developmental research and for cell therapies. In this review we consider the derivation and spontaneous differentiation of human ES cells. 相似文献
23.
汪希 《上海第二医科大学学报》2002,14(2)
Objective In order to improve the in vivo gene transfer into the heart muscle, we have designed a ECG-synchronized microinjection system that allows sequential gene delivery to the myocardium.Methods A cannula was introduced into the right carotid artery of the Wistar rat under general anesthesia.With the ECG-synchronized injection during diastole, the genetic vector (Ad CMV lacZ ) infusion was performed with various concentrations( l07 ~ l010pfu ) and different frequency ( the ratio of heart beats per injection from 1: 1 to 4: 1 ). The hearts of the rats were removed after 7 days for histological examination. Results Best results were obtained with a total vector amount of l09 pfu and a good ratio 3: 1 between heart frequency and injection frequency. The transfection efficiency was increased by use of vasodilators and by an increase of vascular permeability. No signs of myocardial ischemia or ventricular arrythmia were observed. Conclusion We have established a novel and safe method for in vivo gene transfer into the heart. Transgene expression suggests that this method may be useful technique to study cardiac function of treat cardiac diseases by means of gene theratpy. 相似文献
24.
白细胞介素-18基因修饰的胎肝细胞经脾移植对小鼠免疫功能的影响 总被引:2,自引:1,他引:1
目的:观察表达mIL-18的重组腺病毒基因修饰的胎肝细胞(AdmIL-18/BNL.CL2)经脾移植对正常小鼠免疫功能的影响。方法:实验组小鼠经脾移植AdmIL-18/BNL.CL2,同时设LacZ病毒对照组(Ad-LacZ/BNL.CL2),BNL.CL2细胞对照组及空白对照组。2周后处死,留取血清,制备腹腔巨噬细胞、脾淋巴细胞、肝组织匀浆液,提取肝组织总RNA。采用ELISA法检测各组小鼠血清、腹腔Mφ和脾细胞培养上清、肝匀浆中细胞因子的含量;采用半定量RT-PCR法,检测肝组织细胞因子mRNA相对表达量;以LDH释放法测定腹腔Mφ杀伤活性和脾NK细胞活性,用MTT还原比色法测定脾淋巴细胞的增殖活性。结果:实验组小鼠血清、细胞培养上清及肝匀浆中,IL-18、IL-2、IFN-γ、TNF-α稔均高于其它对照组,而IL-4、IL-10水平则低于对照组;半定量RT-PCR结果与ELISA检测结果一致;同时,实验组腹腔Mφ的杀伤活性和脾NK细胞活性,及脾淋巴细胞增殖活性也明显高于对照组。结论:AdmIL-18能有效转染至胎肝细胞并稳定表达mIL-18;AdmIL-18基因修饰的胎肝细胞经脾移植后,可显著提高肝脏、脾脏免疫细胞活性,活化腹腔Mφ,促进Th1类细胞因子表达,抑制Th2类细胞因子的分泌。 相似文献
25.
Rats were trained in a Y-maze on a two-choice simultaneous black-white discrimination with either black or white as S+. Animals were then transferred to one of three discrimination tasks. In task 1 (New S–), a new stimulus, either vertical or horizontal stripes, was substituted for the original S–. In task 2 (New S+), a new stimulus, either vertical or horizontal stripes as in task 1, was substituted for the original S+. In task 3 (New S+/S–) animals were trained on horizontal-vertical discrimination. The pre-trial administration of 1 mg/kg d-amphetamine facilitated the acquisition of the original black-white discrimination with both black as S+ and white as S+. Likewise, the drug improved performance in all three transfer conditions. However, the course of learning in the three transfer tasks was different in the placebo- and amphetamine-treated animals. Amphetamine-treated animals were disrupted more by a change in S+ than by a change in S–, whereas the opposite pattern was evident in the placebo controls. When both discriminative stimuli were changed, placebo animals exhibited pronounced decrement in performance, whereas amphetamine animals exhibited excellent learning. The implications of these findings for the effects of amphetamine on discrimination learning are discussed. 相似文献
26.
Balanced steady-state free precession (bSSFP) has become increasingly important in clinical applications. Its signal properties have been investigated over several years by many groups, and various critical factors for bSSFP signal intensity and stability, such as off-resonances, flow, and eddy currents, have been identified. It is generally accepted that bSSFP signal intensity is a function of relaxation times, excitation angles, and spin densities only. While this is true for simple phantoms, it appears that signals from tissues are significantly less intense than predicted by theory. This work demonstrates that the molecular origin of this apparent signal reduction is due to on-resonance magnetization transfer (MT). High flip angles in combination with very short repetition times (TRs), as commonly used for bSSFP, lead to a considerable saturation in the fraction of macromolecular (MM) pool protons. As a result, bSSFP signal is strongly attenuated by up to a factor of 2 in the human brain compared to the signal expected from theory. 相似文献
27.
D. Grant Richards Kevin G. Whithear Peter C. Scott Robin B. Gasser 《Acta parasitologica / Witold Stefański Institute of Parasitology, Warszawa, Poland》2006,51(2):156-159
Coccidiosis of chickens, caused by species of Eimeria (Protozoa, Apicomplexa), is an intestinal disease of major economic importance worldwide. In the present study, the reproductive
characteristics of a precocious line (designated E. tenella Rt3+15) from Australia were investigated in chicken embryos and the implications of the findings briefly discussed. 相似文献
28.
[目的]探讨腓浅神经浅支修复桡神经缺损的临床效果。[方法]对腓浅神经浅支与桡神经形态结构进行比较,并对腓浅神经浅支移植修复桡神经缺损性损伤5例进行临床分析。[结果]腓浅神经浅支与桡神经形态结构大体一致.5例病例平均随访11(8~26)个月.按文献标准评定,优3例,良2例。[结论]腓浅神经浅支可作为修复桡神经缺损理想的供体神经。 相似文献
29.
目的制备胶原蛋白一明胶神经支架材料(CG材料)并研究其在修复大鼠10mm坐骨神经缺损实验中的疗效。方法以I型胶原蛋白、明胶通过冷冻干燥技术制备具有轴向微管结构的神经支架材料,用其桥接修复sD大鼠坐骨神经10mm缺损。术后16周分别行透射电镜,S-100、β-tubulin class Ⅲ、NFl60免疫荧光染色以及电生理检测,观察支架材料引导神经再生的疗效。结果制备的材料内部为孔径均匀且平行排列的微管结构,术后16周通过透射电镜和免疫荧光染色可见大量再生神经纤维,电生理检测神经传导速度及波幅接近自体神经移植。结论胶原蛋白一明胶支架材料能够有效的促进周围神经再生。 相似文献
30.
17β-雌二醇对子宫内膜异位症患者在位子宫内膜间质细胞β-catenin mRNA和蛋白表达的影响 总被引:2,自引:0,他引:2
目的研究17β-雌二醇(17β-E2)对子宫内膜异位症(内异症)患者在位子宫内膜间质细胞β-catenin mRNA和蛋白表达的影响,探讨Wnt/β-catenin信号通路在介导雌激素促进内异症发生发展的作用。方法体外分离培养内异症患者在位子宫内膜间质细胞。用不同浓度17β-E2处理子宫内膜间质细胞48 h;此后选用10-10mol/L 17β-E2处理子宫内膜间质细胞12、24和48 h,逆转录聚合酶链反应(RT-PCR)和免疫印迹法(Western blotting)检测17β-E2处理前后子宫内膜间质细胞β-catenin mRNA和蛋白的表达水平。同法分析雌激素受体拮抗剂ICI182,780(10-6mol/L)对17β-E2促进β-catenin mRNA和蛋白表达的影响。免疫组织化学染色观察17β-E2作用后β-catenin在子宫内膜间质细胞中的定位。结果17β-E2能明显促进内异症患者在位子宫内膜间质细胞β-catenin mRNA和蛋白的表达,并呈剂量和时间依赖性,于10-10mol/L作用48 h最明显。雌激素受体拮抗剂ICI182,780能明显抑制17β-E2对子宫内膜间质细胞β-catenin mRNA和蛋白的表达。免疫组织化学染色发现17β-E2能促进β-catenin在子宫内膜间质细胞核内的表达。结论雌激素可能通过激活Wnt/β-catenin信号通路促进内异症在位子宫内膜的异位种植。 相似文献