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Configural processing of different topologically structured figures: an ERP study. 不同拓扑结构图形的构形处理:一项ERP研究。
Pub Date : 2009-12-01 Epub Date: 2009-12-17 DOI: 10.1007/s11427-009-0150-0
JunJun Zhang, WeiNa Zhu, XiaoJun Ding, ChangLe Zhou, XinTian Hu, YuanYe Ma

According to Chen's theory, topological differences are perceived faster than feature differences in early visual perception. We hypothesized that topological perception is caused by the sensitivity in discriminating figures with and without "holes". An ERP experiment was conducted utilizing a passive paradigm to investigate the differences in perceiving figures with "hole" and with "no-hole". The results showed differences in N170 components between figures with "holes" and with "no-holes". The inversion of the "hole" could influence the latency of N170, but the inversion of the "no-hole" could not, which indicated that global features are processed first in the "hole" perception whilst local features are given priority to the "no-hole" perception. This result was similar to studies concerning face and non-face objects, suggesting a configural processing of the "hole".

根据Chen的理论,在早期视觉感知中,拓扑差异比特征差异被感知得更快。我们假设拓扑感知是由区分有和没有“孔”的图形的敏感性引起的。采用被动范式进行ERP实验,探讨被试对“有洞”和“无洞”图形的感知差异。结果表明,“孔”与“无孔”的N170成分存在差异。“洞”的反转会影响N170的潜伏期,而“无洞”的反转则不会,说明“洞”感知优先处理全局特征,“无洞”感知优先处理局部特征。这一结果与人脸和非人脸物体的研究结果相似,表明对“洞”进行了构形加工。
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引用次数: 2
Circulating miRNA and cancer diagnosis. 循环miRNA与癌症诊断。
Pub Date : 2009-12-01 Epub Date: 2009-12-17 DOI: 10.1007/s11427-009-0158-5
Yi Tie, BinDong Liu, HanJiang Fu, XiaoFei Zheng

miRNAs are a class of small RNA molecules with regulatory function, and play an important role in tumor development and progression. It has been demonstrated that tumor-derived miRNAs exist in the circulating nucleic acids of cancer patients. This phenomenon implies that detection of the circulating miRNA may be an effective method for non-invasive diagnosis of cancer. In this review, we summarize the applications of the circulating miRNA as biomarkers in cancer diagnosis, as well as the latest research progress in this area.

miRNAs是一类具有调控功能的小RNA分子,在肿瘤的发生发展中起着重要作用。肿瘤来源的mirna存在于癌症患者的循环核酸中。这一现象提示检测循环miRNA可能是一种有效的非侵入性癌症诊断方法。本文就循环miRNA作为生物标志物在肿瘤诊断中的应用及最新研究进展进行综述。
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引用次数: 33
Global transcriptional profiles of Trichophyton rubrum in response to Flucytosine. 红毛藓对氟胞嘧啶反应的全球转录谱。
Pub Date : 2009-12-01 Epub Date: 2009-12-17 DOI: 10.1007/s11427-009-0153-x
Rong Zhao, Wen Bin, YouJiang Diao, Jian Yang, Tao Liu, JunPing Peng, Qi Jin

Trichophyton rubrum (T.rubrum) is one of the most common human fungal pathogens that cause chronic infections of the skin and nails. To identify antifungal responsive genes, cDNA microarray analysis was performed for T. rubrum to reveal global transcriptional profiles of drug-specific responses to 5-Flucytosine (5-FC). cDNA microarray was constructed from the T. rubrum expressed sequence tag (ESTs) database, the minimum inhibitory concentration (MIC) of 5-FC was determined, and microarray hybridization and data analysis were applied. The expression pattern of 7 genes observed by microarray was confirmed by the quantitative real-time reverser transcription polymerase chain reaction (RT-PCR). Data analysis indicated that a total of 474 genes were found differentially expressed, 196 showed an increase in expression and 278 showed a decrease in expression. Marked down-regulation of genes involved in nucleotide metabolism (such as CDC21), transcription (such as E2F1), and RNA processing (such as SGN1, RIM4 and NOP1) was observed. Other genes involved in signal transduction, chaperones, inorganic ion transport, secondary metabolite biosynthesis, amino acid transport, lipid transport and potential drug resistance mechanism were also affected by 5-FC. Quantitative real-time RT-PCR of the selected genes confirmed the reliability of the microarray results. This is the first analysis of transcriptional profiles in response to 5-FC for T. rubrum. The findings may be valuable for the identification of genes involved in mechanisms of action and mechanisms of antifungal drug resistance of 5-FC.

红毛霉(T.rubrum)是最常见的人类真菌病原体之一,可引起皮肤和指甲的慢性感染。为了鉴定抗真菌应答基因,研究人员对T. rubrum进行了cDNA芯片分析,以揭示5-氟胞嘧啶(5-FC)药物特异性应答的全球转录谱。利用红毛毡表达序列标签(est)数据库构建cDNA芯片,测定5-FC的最小抑制浓度(MIC),并进行芯片杂交和数据分析。通过实时定量逆转录聚合酶链反应(RT-PCR)证实了芯片观察到的7个基因的表达模式。数据分析表明,共有474个基因存在差异表达,其中196个基因表达增加,278个基因表达减少。参与核苷酸代谢(如CDC21)、转录(如E2F1)和RNA加工(如SGN1、RIM4和NOP1)的基因显著下调。其他参与信号转导、伴侣、无机离子转运、次生代谢物生物合成、氨基酸转运、脂质转运和潜在耐药机制的基因也受到5-FC的影响。所选基因的实时定量RT-PCR证实了芯片结果的可靠性。这是首次对红毛霉对5-FC的转录谱进行分析。这些发现可能对鉴定5-FC的作用机制和抗真菌耐药机制相关基因有价值。
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引用次数: 5
microRNA-181b通过靶定 MLK2 调节白血病细胞HL-60的增殖 microRNA-181b通过靶定 MLK2 调节白血病细胞HL-60的增殖
Pub Date : 2009-11-20 DOI: 10.1360/ZC2009-39-11-1034
米延 陈宏陈群方明, Chen Qun Fang Meng Mi Yan Chen Hong
microRNA在细胞的转移、凋亡、分化等生命过程中发挥着重要的作用. miR-181b在急髓性白血病组织中高表达, 通过靶定MLK2调节急髓性白血病细胞的增殖. 本结果提示, miR-181b在急髓性白血病的生物学过程发挥着重要的作用, 同时为急髓性白血病的治疗提供了新的解决方案.
microRNA在细胞的转移、凋亡、分化等生命过程中发挥着重要的作用. miR-181b在急髓性白血病组织中高表达, 通过靶定MLK2调节急髓性白血病细胞的增殖. 本结果提示, miR-181b在急髓性白血病的生物学过程发挥着重要的作用, 同时为急髓性白血病的治疗提供了新的解决方案.
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引用次数: 0
体外模拟脑缺血再灌注条件下BV-2细胞TLR4 信号途径对TLR2表达的影响 体外模拟脑缺血再灌注条件下BV-2细胞TLR4 信号途径对TLR2表达的影响
Pub Date : 2009-11-20 DOI: 10.1360/ZC2009-39-11-1013
孙鹏 张清 韩继媛 田元 张景辉, Zhang Qing Han Ji-Yuan Tian Yuan Zhang Jing-Hui Sun Feng
研究证实, TLR4和TLR2有可能作为重要炎性受体介导脑缺血再灌注炎性损伤. 然而目前还不清楚在此过程中TLR2和TLR4受体之间是否存在着交叉对话可能. 本研究首先利用针对TLR4基因的RNA干扰技术阻断体外模拟脑I/R条件下BV-2细胞TLR4信号传导途径, 观察此时TLR2受体表达变化, 初步探讨TLR4信号途径对TLR2表达的影响. 然后利用NF-κB抑制剂PDTC阻断NF-κB活性来观察体外模拟脑I/R条件下BV-2细胞TLR2和TLR4受体表达变化, 进一步阐明NF-κB在TLR2和TLR4交叉对话中的作用. 结果表明: (1) 体外模拟脑I/R条件下阻断BV-2细胞TLR4信号传导途径可以明显抑制TLR2和NF-κB表达的上调; (2) PDTC预处理后在体外模拟脑I/R条件下BV-2细胞 TLR2和TLR4的表达均下调. 结果提示, 脑I/R损伤中TLR4受体激活后有可能通过NF-κB的介导, 进一步影响TLR2的表达, 从而导致炎症反应的链式放大, 两者协同加重了脑损伤的过程.
研究证实, TLR4和TLR2有可能作为重要炎性受体介导脑缺血再灌注炎性损伤. 然而目前还不清楚在此过程中TLR2和TLR4受体之间是否存在着交叉对话可能. 本研究首先利用针对TLR4基因的RNA干扰技术阻断体外模拟脑I/R条件下BV-2细胞TLR4信号传导途径, 观察此时TLR2受体表达变化, 初步探讨TLR4信号途径对TLR2表达的影响. 然后利用NF-κB抑制剂PDTC阻断NF-κB活性来观察体外模拟脑I/R条件下BV-2细胞TLR2和TLR4受体表达变化, 进一步阐明NF-κB在TLR2和TLR4交叉对话中的作用. 结果表明: (1) 体外模拟脑I/R条件下阻断BV-2细胞TLR4信号传导途径可以明显抑制TLR2和NF-κB表达的上调; (2) PDTC预处理后在体外模拟脑I/R条件下BV-2细胞 TLR2和TLR4的表达均下调. 结果提示, 脑I/R损伤中TLR4受体激活后有可能通过NF-κB的介导, 进一步影响TLR2的表达, 从而导致炎症反应的链式放大, 两者协同加重了脑损伤的过程.
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引用次数: 0
Proteomic analysis of mitochondria reveals a metabolic switch from fatty acid oxidation to glycolysis in the failing heart. 线粒体的蛋白质组学分析揭示了衰竭心脏从脂肪酸氧化到糖酵解的代谢转换。
Pub Date : 2009-11-01 Epub Date: 2009-11-24 DOI: 10.1007/s11427-009-0140-2
Jun Wang, Ling Bai, Jing Li, ChaoFeng Sun, Jin Zhao, ChangCong Cui, Ke Han, Yu Liu, XiaoZhen Zhuo, TingZhong Wang, Ping Liu, FenLing Fan, YouFei Guan, AiQun Ma

This work characterizes the mitochondrial proteomic profile in the failing heart and elucidates the molecular basis of mitochondria in heart failure. Heart failure was induced in rats by myocardial infarction, and mitochondria were isolated from hearts by differential centrifugation. Using two-dimensional gel electrophoresis and matrix-assisted laser desorption/ionization-time of flight mass spectrometry, a system biology approach was employed to investigate differences in mitochondrial proteins between normal and failing hearts. Mass spectrometry identified 27 proteins differentially expressed that involved in energy metabolism. Among those, the up-regulated proteins included tricarboxylic acid cycle enzymes and pyruvate dehydrogenase complex subunits while the down-regulated proteins were involved in fatty acid oxidation and the OXPHOS complex. These results suggest a substantial metabolic switch from free fatty acid oxidation to glycolysis in heart failure and provide molecular evidence for alterations in the structural and functional parameters of mitochondria that may contribute to cardiac dysfunction during ischemic injury.

这项工作表征了衰竭心脏的线粒体蛋白质组学特征,并阐明了心力衰竭线粒体的分子基础。用心肌梗死诱导大鼠心力衰竭,用差速离心法从心脏中分离线粒体。利用二维凝胶电泳和基质辅助激光解吸/电离飞行时间质谱,采用系统生物学方法研究了正常和衰竭心脏之间线粒体蛋白的差异。质谱分析鉴定出27个与能量代谢有关的蛋白表达差异。其中,上调蛋白包括三羧酸循环酶和丙酮酸脱氢酶复合物亚基,下调蛋白涉及脂肪酸氧化和OXPHOS复合物。这些结果表明心力衰竭中存在从游离脂肪酸氧化到糖酵解的实质性代谢转换,并为线粒体结构和功能参数的改变提供了分子证据,这些改变可能有助于缺血性损伤期间心功能障碍。
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引用次数: 21
Effect and mechanism of acute graft versus host disease on early diffuse murine lung injury following allogeneic stem cell transplantation. 同种异体干细胞移植后急性移植物抗宿主病对小鼠早期弥漫性肺损伤的影响及机制
Pub Date : 2009-11-01 Epub Date: 2009-11-24 DOI: 10.1007/s11427-009-0139-8
Juan Ning, Qi Fa Liu, Xiao Dan Luo, Zhi Ping Fan, Yu Zhang

To explore the effect and pathogenssis of acute graft-versus-host disease (aGVHD) on early diffuse lung injury in allogeneic hematopoietic stem cell transplantation (allo-HSCT), we established an aGVHD model of C(57)BL/6-->BALB/c mice. Chest computed tomography (CT) scans, histopathology and the levels of cytokines including tumor necrosis factor alpha (TNFalpha) and Interferon (IFNgamma) in lungs were dynamically detected in recipient mice after transplantation. The incidence of aGVHD was respectively 0%, 0% and 100% in simple irradiation group (A), syngeneic transplant group(B) and allogeneic transplant group (C). Chest CT scans of recipient mice were normal in 3 groups on days +3 and +7 after transplantation. CT showed that two of ten mice had bilateral lung diffuse infiltrate on day +12 (on the brink of death) in group A and 6 of 10 mice had bilateral lung diffuse infiltrate on day +14 (3 d after aGVHD occurring) in group C, and were normal on days +12 and +14 in group B after transplantation. Histopathology of lungs in the 3 groups was similar, consisting of minor interstitial pneumonitis on day +3. Group A showed edema, hyperplasia of epithelial cells and widened alveolar interval on day +7, and epithelial cell necrosis, lymphocyte infiltration, hemorrhage, protein leakage, and local consolidation on day +12. The histopathology of group B showed slight edema of epithelial cells on +7 day, which were slighter than that on day +3, and virtually normal on day +14. The histopathology in group C was characterized by the significant expansion and congestion of capillaries, and lymphocyte infiltration on day +7, the acute pneumonitis was present involving tissue edema, lymphocyte and macrophage infiltration, protein leakage and perivascular inflammation on day +14. In group A, the levels of TNFalpha were lower on day +7 than on day +3. In group B, the levels of TNFalpha attained a peak on day +3, which decreased on days +7 and +14. In group C, the levels of TNFalpha were highest on day +7 and there was a significant difference between those on days +7 and +14 (P=0.816). In group A, the levels of IFNgamma on day +7 were higher than on day +3. In group B, the levels of IFNgamma increased progressively, but the comparison of IFNgamma levels in different times had no statistical significance (P=0.521, 0.118, 0.340). In group C, the levels of IFNgamma attained a peak by day +7 and decreased on day +14. aGVHD is the main cause of early non-infectious lung injury. T lymphocytes and TNFalpha are possibly implicated in the pathogenesis of acute GVHD-induced lung injury. The decreased levels of IFNgamma in lung tissues following transplantation might be associated with pulmonary fibrosis in late non-infectious pulmonary complications.

为探讨急性移植物抗宿主病(aGVHD)对同种异体造血干细胞移植(alloo - hsct)早期弥漫性肺损伤的影响及其发病机制,我们建立了C(57)BL/6- >BALB/ C小鼠aGVHD模型。动态检测移植后受体小鼠的胸部计算机断层扫描(CT)、组织病理学和细胞因子水平,包括肿瘤坏死因子α (TNFalpha)和干扰素(IFNgamma)。单纯照射组(A)、同基因移植组(B)、异体移植组(C) aGVHD发生率分别为0%、0%、100%。3组受体小鼠移植后+3、+7天胸部CT扫描正常。CT显示,A组10只小鼠中有2只在移植后+12天(死亡边缘)出现双侧肺弥漫性浸润,C组10只小鼠中有6只在移植后+14天(发生aGVHD后3 d)出现双侧肺弥漫性浸润,B组移植后+12、+14天正常。3组肺组织病理相似,均在第3天出现轻度间质性肺炎。A组在+7天出现水肿、上皮细胞增生、肺泡间隙增宽,+12天出现上皮细胞坏死、淋巴细胞浸润、出血、蛋白渗漏、局部实变。B组在+7天上皮细胞轻度水肿,水肿程度较+3天轻微,+14天基本正常。C组组织病理表现为+7天毛细血管明显扩张充血,淋巴细胞浸润,+14天出现急性肺炎,组织水肿,淋巴细胞和巨噬细胞浸润,蛋白渗漏,血管周围炎症。在A组,第7天TNFalpha水平低于第3天。B组TNFalpha水平在第3天达到峰值,在第7天和第14天下降。C组TNFalpha水平在+7天最高,与+7、+14天差异有统计学意义(P=0.816)。A组在+7天IFNgamma水平高于+3天。B组IFNgamma水平逐渐升高,但不同时间IFNgamma水平比较无统计学意义(P=0.521, 0.118, 0.340)。C组IFNgamma水平在第7天达到峰值,在第14天下降。aGVHD是早期非感染性肺损伤的主要原因。T淋巴细胞和TNFalpha可能与急性gvhd诱导的肺损伤的发病机制有关。移植后肺组织中ifnγ水平的降低可能与晚期非感染性肺并发症中的肺纤维化有关。
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引用次数: 3
Modeling and simulation of ion channels and action potentials in taste receptor cells. 味觉感受器细胞中离子通道和动作电位的建模与模拟。
Pub Date : 2009-11-01 Epub Date: 2009-11-24 DOI: 10.1007/s11427-009-0138-9
PeiHua Chen, Xiao-dong Liu, Wei Zhang, Jun Zhou, Ping Wang, Wei Yang, JianHong Luo

Based on patch clamp data on the ionic currents of rat taste receptor cells, a mathematical model of mammalian taste receptor cells was constructed to simulate the action potentials of taste receptor cells and their corresponding ionic components, including voltage-gated Na(+) currents and outward delayed rectifier K(+) currents. Our simulations reproduced the action potentials of taste receptor cells in response to electrical stimuli or sour tastants. The kinetics of ion channels and their roles in action potentials of taste receptor cells were also analyzed. Our prototype model of single taste receptor cell and simulation results presented in this paper provide the basis for the further study of taste information processing in the gustatory system.

基于膜片钳对大鼠味觉感受器细胞离子电流的测量数据,建立了哺乳动物味觉感受器细胞的数学模型,模拟了味觉感受器细胞及其相应离子组分的动作电位,包括电压门控Na(+)电流和向外延迟整流K(+)电流。我们的模拟再现了味觉受体细胞对电刺激或酸味剂的反应的动作电位。并分析了离子通道的动力学及其在味觉受体细胞动作电位中的作用。本文建立的单个味觉受体细胞的原型模型和模拟结果为进一步研究味觉系统中的味觉信息加工提供了基础。
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引用次数: 3
The expression profile of genes in rice roots under low phosphorus stress. 低磷胁迫下水稻根系基因表达谱研究。
Pub Date : 2009-11-01 Epub Date: 2009-11-24 DOI: 10.1007/s11427-009-0137-x
LiHua Li, XuHua Qiu, XiangHua Li, ShiPing Wang, XingMing Lian

Phosphorus (P) is one of the most essential macronutrients required for plant growth. Although it is abundant in soil, P is often the limiting nutrient for crop yield potential because of the low concentration of soluble P that plants can absorb directly. The gene expression profile was investigated in rice roots at 6, 24 and 72 h under low P stress and compared with a control (normal P) profile, using a DNA chip of 60000 oligos (70 mer) that represented all putative genes of the rice genome. A total of 795 differentially expressed genes were identified in response to phosphate (Pi) starvation in at least one of the treatments. Based on the analysis, we found that: (i) The genes coding for the Pi transporter, acid phosphatase and RNase were up-regulated in rice roots; (ii) the genes involved in glycolysis were first up-regulated and then down-regulated; (iii) several genes involved in N metabolism and lipid metabolism changed their expression patterns; (iv) some genes involved in cell senescence and DNA or protein degradation were up-regulated; and (v) some transmembrane transporter genes were up-regulated. The results may provide useful information in the molecular process associated with Pi deficiency and thus facilitate research in improving Pi utilization in crop species.

磷(P)是植物生长所必需的大量营养元素之一。虽然磷在土壤中含量丰富,但由于植物能直接吸收的可溶性磷浓度低,往往是限制作物产量潜力的养分。利用60000个寡核苷酸(70 mer)的DNA芯片,研究了低磷胁迫下水稻根系6、24和72 h的基因表达谱,并与对照(正常磷胁迫)的基因表达谱进行了比较。在至少一种处理中,共鉴定出795个差异表达基因对磷酸盐(Pi)饥饿的响应。结果表明:(1)水稻根系中Pi转运体、酸性磷酸酶和RNase编码基因表达上调;(ii)糖酵解相关基因先上调后下调;(iii)多个参与氮代谢和脂质代谢的基因表达模式发生改变;(iv)部分参与细胞衰老和DNA或蛋白质降解的基因上调;(5)部分跨膜转运蛋白基因表达上调。研究结果可为了解缺磷的分子过程提供有用信息,从而为研究如何提高作物对缺磷的利用提供依据。
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引用次数: 20
Origin and domestication history of Peking ducks deltermined through microsatellite and mitochondrial marker analysis. 通过微卫星和线粒体标记分析确定了北京鸭的起源和驯化历史。
Pub Date : 2009-11-01 Epub Date: 2009-11-24 DOI: 10.1007/s11427-009-0145-x
LuJiang Qu, Wei Liu, FangXi Yang, ZhuoCheng Hou, JiangXia Zheng, GuiYun Xu, Ning Yang

In order to elucidate the domestication history of Peking ducks, 190 blood samples from six Chinese indigenous duck breeds were collected with 186 individuals genotyped by 15 microsatellite markers. Both the F(ST) and Nei's standard genetic distances (D(s)) from the microsatellite data indicated high genetic differentiation between Peking duck and other Chinese indigenous breeds. The haplotype network with mtDNA data showed that most of the Peking duck haplotypes were distinctly different from those of other domestic breeds. Although the H01 haplotype was shared by all domesticated duck breeds, Peking ducks displayed 12 specific domestic duck haplotypes, including four similar haplotypes H02, H04, H08 and H22, that formed a single haplogroup (A). Both H02 and H22 haplotypes were also shared by mallard and Peking ducks, indicating that Peking ducks originated from wild mallard ducks.

为了阐明北京鸭的驯化历史,本研究收集了6个中国地方鸭品种190份血样,用15个微卫星标记对186个个体进行了基因分型。微卫星数据的F(ST)和Nei’s标准遗传距离(D(s))均表明北京鸭与中国其他地方品种存在高度遗传分化。利用mtDNA数据建立的单倍型网络显示,北京鸭的大部分单倍型与其他家养品种有明显差异。虽然所有家鸭品种都具有H01单倍型,但北京鸭表现出12个特定的家鸭单倍型,其中包括H02、H04、H08和H22 4个相似的单倍型,它们形成了一个单倍群(a)。绿头鸭和北京鸭也具有相同的H02和H22单倍型,说明北京鸭起源于野生绿头鸭。
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引用次数: 21
期刊
Science in China. Series C, Life Sciences / Chinese Academy of Sciences
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