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Optimisation of a Holographic Microscope for Microbial Study 微生物研究用全息显微镜的优化
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.117
B. Niraula, J. Nadeau
Background: Tracking of microbial organisms over a volume requires images at multiple focal planes along the orthogonal direction. With most conventional microscopes, this requires repeated readjustments; using Digital Holographic Microscopy (DHM), it is possible to use a set of interference patterns to reconstruct at various distances, thereby creating a 3D stack based off a single image. Methods: We used an off-axis Mach-Zehnder DHM for imaging and tracking bacterial movement. We describe the algorithm employed for tracking, as well as our improvement of trackability by testing differences in image contrast with the use of Quantum Dots. Results: We show that the use of Quantum Dots resulted in an increase in contrast of approximately 11%. Conclusion: We suggest this as a method of increasing resolvability of individual microbes. With a more compact design, the microscope will be applicable in various fields, and can be used remotely for studies of microbial organisms.
背景:在一个体积上跟踪微生物需要沿正交方向在多个焦平面上的图像。对于大多数传统显微镜,这需要反复调整;使用数字全息显微镜(DHM),可以使用一组干涉图案在不同距离上进行重建,从而基于单个图像创建3D堆栈。方法:我们使用离轴Mach-Zehnder DHM进行成像和跟踪细菌运动。我们描述了用于跟踪的算法,以及我们通过使用量子点测试图像对比度的差异来改进可跟踪性。结果:我们表明,量子点的使用导致对比度增加了大约11%。结论:我们认为这是一种提高单个微生物可分解性的方法。该显微镜具有更紧凑的设计,将适用于各个领域,并可远程用于微生物生物的研究。
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引用次数: 0
Promise of Mindfulness-Based Interventions as Therapies to Prevent Cognitive Decline 以正念为基础的干预有望成为预防认知衰退的疗法
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.123
Daniel M. Sapozhnikov
Background: Alzheimer’s disease (AD) is a neurodegenerative disorder that affects 5 million United States citizens. Many authors have proposed that mindfulness-based interventions (MBIs) have the potential to effectively prevent AD-associated pathology and symptomology. However, the fact that both meditation and AD are complex processes that involve a great number of biological pathways has made these phenomena particularly challenging to dissect. This review advocates the use of gene expression to investigate the mechanisms by which MBIs combat AD pathology. Methods: Searches were performed using Thomson Reuters Web of Science. Ultimately, 85 journal articles were selected for their content as it pertains to the purpose of this review. Summary: Peripheral blood mononuclear cells (PBMCs) may provide reliable measures of cerebral gene expression. Profiling their gene expression has demonstrated that MBIs may produce gene expression changes in many of the same pathways (inflammation, cellular stress, proliferation, synaptic function) and often in the opposite direction of disease-related deregulation. While AD is marked by shortened telomeres resulting in genetic turmoil, meditation has been documented to exhibit a positive effect on telomere maintenance. A comprehensive gene expression investigation is invaluable to reveal relevant molecular mechanisms and provide the foundation for exploring the interaction between MBI and AD.
背景:阿尔茨海默病(AD)是一种神经退行性疾病,影响着500万美国公民。许多作者提出,正念干预(MBIs)具有有效预防ad相关病理和症状的潜力。然而,冥想和AD都是复杂的过程,涉及大量的生物途径,这使得这些现象特别具有挑战性。这篇综述提倡使用基因表达来研究mbi对抗AD病理的机制。方法:使用Thomson Reuters Web of Science进行检索。最终,85篇期刊文章被选中,因为它们的内容与本综述的目的有关。摘要:外周血单个核细胞(PBMCs)可以提供可靠的大脑基因表达指标。对其基因表达的分析表明,mbi可能在许多相同的途径(炎症、细胞应激、增殖、突触功能)中产生基因表达变化,并且通常与疾病相关的解除管制的方向相反。虽然阿尔茨海默病的特点是端粒缩短,导致基因混乱,但冥想对端粒的维持有积极的影响。全面的基因表达研究对于揭示相关分子机制,为探索MBI与AD的相互作用奠定基础具有重要意义。
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引用次数: 1
Cadmium(II) Chalcogenides Stable across Wide Temperature Range 镉(II)硫族化合物在宽温度范围内稳定
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.115
Jacqueline Riddle, J. Bayne, I. Butler
Background: The three cadmium(II) chalcogenides CdX (X = S, Se, Te; Cadmium with either Sulphur, Se- lenium, or Tellurium), have important applications as artists’ pigments and in the electronics industry. The purpose of this study is to assess the structural stabilities of bulk, microcrystalline samples of the three cadmium(II) chalcogenides over a wide temperature range by examining the changes that occur in their Raman spectra. Methods: We recorded the Raman spectra of the three cadmium(II) chalcogenides from -196 °C to 500 °C on a commercial instrument equipped with a microscope and a variable-temperature stage. Results: While the Raman spectra of all three cadmium(II) chalcogenides exhibited significant peak shifts and broadening with increasing temperature, these effects were completely reversible. There is no evidence of phase transitions, indicating structural stability. Conclusion: Taken together, our results show that the three cadmium(II) chalcogenides are resistant to structural changes throughout the almost -700 °C temperature range investigated, thereby reinforcing their continued use in artwork and in the electronics industry.
背景:三种镉(II)硫属化合物CdX (X = S, Se, Te;镉(含硫、硒或碲)作为艺术家的颜料和电子工业有重要的应用。本研究的目的是通过检查三种镉(II)硫族化合物的拉曼光谱变化,评估其体微晶样品在宽温度范围内的结构稳定性。方法:在配有显微镜和变温台的商用仪器上记录3种镉(II)硫族化合物在-196 ~ 500℃范围内的拉曼光谱。结果:虽然三种镉硫族化合物的拉曼光谱随温度的升高均表现出明显的峰移和展宽,但这些影响是完全可逆的。没有相变的证据,表明结构稳定。综上所述,我们的研究结果表明,三种镉(II)硫族化合物在几乎-700°C的温度范围内都能抵抗结构变化,从而加强了它们在艺术品和电子工业中的继续使用。
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引用次数: 0
Earth Infrared Radiation Spectra During Global Warming Hiatus 全球变暖中断期间的地球红外辐射光谱
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.116
Jean-Franois Blanchette, Yi Huang
Background: Since 1997-98, observations of annual mean surface temperature have shown a slowdown of global temperature increases, suggesting a hiatus in global warming. Given this finding, we are interested in diagnosing trends in the Earth’s outgoing longwave radiation (OLR) spectrum throughout the last decade. Methods: We calculated the trend in OLR measured by the Atmospheric Infrared Sounder (AIRS) aboard NASA’s Aqua satellite between 2003 and 2013, and compared these results with the trend in atmospheric and surface temperature and tropospheric absolute humidity, obtained from AIRS retrieval product and from the ECMWF (European Center for Medium range Weather Forecasting) Re-Analysis (ERA) interim product. We also isolated the greenhouse effect from the OLR trend by subtracting the amount of surface radiation emitted from the total radiation received by the sounder. Results: The OLR trend is negative in the CO2 absorption band, negative in the window spectral region, and positive in the water vapor band. The trend in surface and tropospheric temperature is negative, as is the trend in tropospheric absolute humidity. The greenhouse effect is increasing in the CO2 band, generally slightly increasing in the window region, and decreasing in the H2O band. Conclusion: Our results show that the CO2 forcing was still present globally through the last decade, with steadily increasing effects. Contributors to the negative trend in OLR in the window region are a small decrease in surface temperature and a strong decrease in tropospheric temperature, where tropospheric H2O emit radiation to space. The decreasing effect of water vapor in the H2O band is due to decreasing tropospheric humidity. This analysis will allow us to detect the changes in greenhouse gas forcing, to examine the correlated surface temperature response, and to study changes and effects in tropospheric water vapor concentration.
背景:自1997- 1998年以来,对年平均地表温度的观测显示全球温度上升速度放缓,表明全球变暖出现了中断。鉴于这一发现,我们有兴趣在过去十年中诊断地球发射的长波辐射(OLR)频谱的趋势。方法:计算美国宇航局Aqua卫星上大气红外探测器(AIRS) 2003 - 2013年OLR的变化趋势,并与AIRS反演产品和欧洲中期天气预报中心(ECMWF)再分析(ERA)中期产品获得的大气、地表温度和对流层绝对湿度的变化趋势进行比较。我们还通过从探测仪接收的总辐射中减去发射的表面辐射量,将温室效应从OLR趋势中分离出来。结果:CO2吸收波段的OLR趋势为负,窗口光谱区为负,水汽波段为正。地表和对流层温度的趋势是负的,对流层绝对湿度的趋势也是负的。温室效应在CO2波段呈增加趋势,在窗口区总体上略有增加,在H2O波段呈减少趋势。结论:我们的研究结果表明,在过去十年中,CO2强迫在全球范围内仍然存在,并且影响稳步增强。窗口区OLR负趋势的贡献者是地表温度的小幅度下降和对流层温度的强烈下降,对流层H2O向空间发射辐射。水汽在H2O波段的减少作用是由于对流层湿度的减少。这种分析将使我们能够探测温室气体强迫的变化,检验相关的地表温度响应,并研究对流层水汽浓度的变化和影响。
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引用次数: 0
Dementia With Lewy Bodies: An Overview 路易体痴呆:综述
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.122
Bridget Hovendon, Michelle Kaufman
Background: Dementia is a neurocognitive disorder that involves multiple cognitive deficits, including memory impairment. Dementia occurs in a variety of disease processes, including Alzheimer disease (AD) and dementia with Lewy bodies, the two most prevalent neurocognitive diseases. This paper reviews the signs and symptoms, neuropathology, diagnosis, prognosis, and treatment of Dementia with Lewy bodies (DLB). Methods: Terms searched included “Lewy body dementia,” “Lewy body disease,” “cognitive disorders,” and “neurodegenerative diseases.” Priority was given to peer-reviewed sources published within the last five years. Summary: In addition to standard neurocognitive disorder symptoms, patients with DLB present clinically fluctuating cognition, visual hallucinations, and Parkinsonism as well as a variety of other symptoms with lower diagnostic sensitivity. Clinical signs, cognitive assessments, and radiologic imaging are used to diagnose DLB as being distinct from disorders like AD, Parkinson disease dementia (PDD), delirium, and normal aging changes. Interventions for this disease may be pharmacological or non-pharmacological. Pharmacological treatments include cholinesterase inhibitors, Levadopa, and selective serotonin reuptake inhibitors or serotonin-norepinephrine reuptake inhibitors. Non-pharmacological interventions include occupational therapy, cognitive stimulation, and physical activity.
背景:痴呆是一种涉及多种认知缺陷的神经认知障碍,包括记忆障碍。痴呆症发生在多种疾病过程中,包括阿尔茨海默病(AD)和路易体痴呆,这两种最常见的神经认知疾病。本文综述了路易体痴呆(DLB)的体征、症状、神经病理学、诊断、预后和治疗。方法:搜索的术语包括“路易体痴呆”、“路易体病”、“认知障碍”和“神经退行性疾病”。优先考虑近五年内发表的经同行评审的资料。摘要:除了标准的神经认知障碍症状外,DLB患者还表现为临床认知波动、视幻觉、帕金森症以及其他各种诊断敏感性较低的症状。临床症状、认知评估和放射学成像用于诊断DLB,以区分AD、帕金森病痴呆(PDD)、谵妄和正常的衰老变化等疾病。对这种疾病的干预可以是药物或非药物。药物治疗包括胆碱酯酶抑制剂、左旋多巴和选择性血清素再摄取抑制剂或血清素-去甲肾上腺素再摄取抑制剂。非药物干预包括职业治疗、认知刺激和身体活动。
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引用次数: 1
Mutation of the Glc-2 Gene May Confer Dominant Ivermectin Resistance Glc-2基因突变可能导致显性伊维菌素耐药性
Pub Date : 2015-03-31 DOI: 10.26443/msurj.v10i1.118
H. Su, J. Dent
Background: Ivermectin is a widely used anti-parasitic drug that binds to and activates glutamate-gated chloride channels (GluCls), giving it its nematocidal (nematode-killing) properties. Due to excessive use of ivermectin, frequent cases of resistance to this nematicide are being reported, suggesting that ivermectin is beginning to lose its efficacy. This project seeks to study whether a mutation of the glc-2 gene, which encodes for a β subunit of the GluCl channel, confers ivermectin resistance. We hypothesize that a glc-2 mutation achieves nematicide resistance by creating a defective GluCl channel that cannot bind to ivermectin. Methods: We used classical genetics to obtain the desired mutants from stock worms. We then tested the worms for resistance profile using ivermectin sensitivity assays. Finally, we examined in vivo interactions by expressing relevant RNA in a heterologous system and performed electrophysiological recordings. Results: We were able to demonstrate that presence of the defective glc-2 leads to increased resistance profiles when given the chance to associate with select GluClα subunits (e.g. AVR-15). We also demonstrated that co-injection of glc-2 and glc-3 compromises GluCl response to L-glutamate, a critical indicator of channel functionality. Conclusion: Our results lend strong support to our hypothesis that glc-2 is able to interact with certain α subunits of GluCl to confer ivermectin resistance. This finding provides a framework for future dominant ivermectin resistance studies.
背景:伊维菌素是一种广泛使用的抗寄生虫药物,它结合并激活谷氨酸门控氯通道(glucl),使其具有杀线虫(杀死线虫)的特性。由于过度使用伊维菌素,经常报告对这种杀线虫剂产生耐药性的病例,这表明伊维菌素开始失去效力。该项目旨在研究编码葡萄糖通道β亚基的glc-2基因的突变是否赋予伊维菌素耐药性。我们假设一个glc-2突变通过创建一个不能与伊维菌素结合的有缺陷的glc-2通道来实现杀线虫剂耐药性。方法:采用经典遗传学方法从家蚕中获得所需的突变体。然后我们用伊维菌素敏感性试验测试了这些蠕虫的耐药性。最后,我们通过在异种系统中表达相关RNA来检测体内相互作用,并进行电生理记录。结果:我们能够证明,当有机会与选定的glc-2亚基(例如AVR-15)结合时,存在缺陷的glc-2会导致抗性谱增加。我们还证明,glc-2和glc-3的共同注射会损害葡萄糖对l -谷氨酸的反应,这是通道功能的一个关键指标。结论:我们的研究结果有力地支持了我们的假设,即glc-2能够与GluCl的某些α亚基相互作用,从而赋予伊维菌素耐药性。这一发现为未来主要的伊维菌素耐药性研究提供了一个框架。
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引用次数: 0
Preschool children without 7-repeat DRD4 gene more likely to develop disorganized attachment style. 没有7-重复DRD4基因的学龄前儿童更容易形成无组织依恋类型。
Pub Date : 2015-03-01 DOI: 10.26443/msurj.v10i1.120
Justin Graffi, E. Moss, Alexia Jolicoeur-Martineau, Gal Moss, V. Lecompte, Katherine Pascuzzo, Vanessa Babineau, Cathryn Gordon-Green, Viara R. Mileva‐Seitz, K. Minde, R. Sassi, N. Carrey, J. Kennedy, H. Gaudreau, R. Levitan, M. Meaney, A. Wazana
BACKGROUND The current paper aimed to explore the effects of birth weight and the 7-repeat allele in Exon III of the dopamine D4 receptor (DRD4) gene on the development of disorganized attachment, a potential endophenotype of depression. Infants born with low birth weight have been shown to be at higher risk for later neurological impairments, psychological disorders or behavioural problems. The DRD4 gene is critical for the cognitive and emotional processes that are sub-served by neural circuits in the prefrontal cortex. This paper examined the main effect of birth weight and DRD4 on the development of disorganized attachment. METHODS Data was used from the Maternal Adversity, Vulnerability and Neurodevelopment (MAVAN) project. The sample consisted of 251 mother-child dyads with complete data. Attachment style was assessed using the modified separation-reunion procedure. RESULTS There was no main effect for birth weight on disorganized attachment, (b = -0.001, p = 0.998). There was, however, a main effect for the DRD4 7-repeat polymorphism on disorganized attachment (b = -1.120, p = 0.004). LIMITATIONS Compared to studies of similar design, the sample size in this study was relatively small. Additionally, a significant number of subjects did not have complete data. CONCLUSIONS Children without the DRD4 7-repeat allele were more likely to have disorganized attachment than children with the DRD4 7-repeat allele. This indicates that the 7-repeate allele of the DRD4 gene may actually serve as a protective factor against disorganized attachment.
背景本研究旨在探讨出生体重和多巴胺D4受体(DRD4)基因外显子III上7重复等位基因对无序依恋(一种潜在的抑郁症内表型)发展的影响。研究表明,出生时体重过轻的婴儿日后出现神经损伤、心理障碍或行为问题的风险更高。DRD4基因对认知和情感过程至关重要,这些过程由前额皮质的神经回路次级服务。本研究探讨了出生体重和DRD4对无组织依恋发展的主要影响。方法数据来源于母体逆境、脆弱性和神经发育(MAVAN)项目。样本由251对数据完整的母子二人组组成。采用改进的分离-团聚程序评估依恋类型。结果出生体重对无组织依恋无主要影响(b = -0.001, p = 0.998)。然而,DRD4 7-repeat多态性对无组织依恋有主要影响(b = -1.120, p = 0.004)。局限性与类似设计的研究相比,本研究的样本量相对较小。此外,相当数量的受试者没有完整的数据。结论不携带DRD4 7-repeat等位基因的儿童比携带DRD4 7-repeat等位基因的儿童更易发生无组织依恋。这表明DRD4基因的7重复等位基因实际上可能是防止无组织附着的保护因子。
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引用次数: 7
Preschool children without 7-repeat DRD4 gene more likely to develop disorganized attachment style. 没有7-重复DRD4基因的学龄前儿童更容易形成无组织依恋类型。
Justin Graffi, Ellen Moss, Alexia Jolicoeur-Martineau, Gal Moss, Vanessa Lecompte, Katherine Pascuzzo, Vanessa Babineau, Cathryn Gordon-Green, Viara R Mileva-Seitz, Klaus Minde, Roberto Sassi, Normand Carrey, James L Kennedy, Helene Gaudreau, Robert Levitan, Michael Meaney, Ashley Wazana

Background: The current paper aimed to explore the effects of birth weight and the 7-repeat allele in Exon III of the dopamine D4 receptor (DRD4) gene on the development of disorganized attachment, a potential endophenotype of depression. Infants born with low birth weight have been shown to be at higher risk for later neurological impairments, psychological disorders or behavioural problems. The DRD4 gene is critical for the cognitive and emotional processes that are sub-served by neural circuits in the prefrontal cortex. This paper examined the main effect of birth weight and DRD4 on the development of disorganized attachment.

Methods: Data was used from the Maternal Adversity, Vulnerability and Neurodevelopment (MAVAN) project. The sample consisted of 251 mother-child dyads with complete data. Attachment style was assessed using the modified separation-reunion procedure.

Results: There was no main effect for birth weight on disorganized attachment, (b = -0.001, p = 0.998). There was, however, a main effect for the DRD4 7-repeat polymorphism on disorganized attachment (b = -1.120, p = 0.004).

Limitations: Compared to studies of similar design, the sample size in this study was relatively small. Additionally, a significant number of subjects did not have complete data.

Conclusions: Children without the DRD4 7-repeat allele were more likely to have disorganized attachment than children with the DRD4 7-repeat allele. This indicates that the 7-repeate allele of the DRD4 gene may actually serve as a protective factor against disorganized attachment.

背景:本研究旨在探讨出生体重和多巴胺D4受体(DRD4)基因外显子III中7重复等位基因对无序依恋(一种潜在的抑郁症内表型)发展的影响。研究表明,出生时体重过轻的婴儿日后出现神经损伤、心理障碍或行为问题的风险更高。DRD4基因对认知和情感过程至关重要,这些过程由前额皮质的神经回路次级服务。本研究探讨了出生体重和DRD4对无组织依恋发展的主要影响。方法:数据来源于母体逆境、脆弱性和神经发育(MAVAN)项目。样本由251对数据完整的母子二人组组成。采用改进的分离-团聚程序评估依恋类型。结果:出生体重对无组织依恋无主要影响(b = -0.001, p = 0.998)。然而,DRD4 7-repeat多态性对无组织依恋有主要影响(b = -1.120, p = 0.004)。局限性:与类似设计的研究相比,本研究的样本量相对较小。此外,相当数量的受试者没有完整的数据。结论:无DRD4 7-repeat等位基因的儿童比有DRD4 7-repeat等位基因的儿童更容易出现无组织依恋。这表明DRD4基因的7重复等位基因实际上可能是防止无组织附着的保护因子。
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引用次数: 0
Human Health and the Microbiota: Interactions Between Gut Microbes, Hygiene, and The Immune System 人类健康和微生物群:肠道微生物、卫生和免疫系统之间的相互作用
Pub Date : 2014-04-30 DOI: 10.26443/msurj.v9i1.161
S. Fukada
Background: In the past, much of the scientific research on microbes focused on mechanisms of infection and disease. This was not in vain, as we gained valuable knowledge about our immune system, as well as the ability to develop vaccines and antibiotics. However, the relationship between humans and microbes is complex. These species have been co-evolving since multicellular organisms evolved on Earth. Summary: Recently, it is beginning to be appreciated that the majority of relationships between humans and microbes are beneficial. From this follows an understanding that beneficial microbes are vital to the normal physiological development of our gut and immune system. This beneficial relationship between the human host and the multitude of microbial communities is well established. However, currently in the developed world epidemiological studies are showing dramatic increases in autoimmunity, allergies, and obesity. It is thus suggested that within westernized societies hygiene is altering the relationship between the gut and the human host in a way that makes humans susceptible to conditions not seen in less developed countries. This understanding advanced the “hygiene hypothesis,” and more recently the, “old friends hypothesis” and “disappearing microbiota hypothesis” as possible explanations for the observed epidemiological phenomena. What follows is a review of the relationship between gut microbes and the host’s immune system, with a focus on how hygiene (antibiotics, chlorination of water, etc.) is beginning to alter this relationship. This review concludes that a further understanding of how hygiene affects the relationship between humans and microbes will be crucial for developing effective therapies considerate of our microbial friends.
背景:过去,许多关于微生物的科学研究都集中在感染和疾病的机制上。这并没有白费,因为我们获得了有关免疫系统的宝贵知识,以及开发疫苗和抗生素的能力。然而,人类和微生物之间的关系是复杂的。自从多细胞生物在地球上进化以来,这些物种一直在共同进化。最近,人们开始认识到人类和微生物之间的大多数关系是有益的。由此得出的理解是,有益微生物对我们肠道和免疫系统的正常生理发育至关重要。人类宿主与众多微生物群落之间的这种有益关系已得到充分证实。然而,目前在发达国家,流行病学研究显示,自身免疫、过敏和肥胖的人数急剧增加。因此,这表明在西方化的社会中,卫生正在改变肠道与人类宿主之间的关系,使人类容易受到欠发达国家所没有的疾病的影响。这种理解推动了“卫生假说”,以及最近的“老朋友假说”和“微生物群消失假说”,作为对观察到的流行病学现象的可能解释。以下是对肠道微生物和宿主免疫系统之间关系的回顾,重点是卫生(抗生素、氯化水等)如何开始改变这种关系。这篇综述的结论是,进一步了解卫生如何影响人类和微生物之间的关系,对于开发考虑到我们的微生物朋友的有效疗法至关重要。
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引用次数: 0
Development of a Cellular System to Identify Modulators of B-Raf Induced Senescence in Human Fibroblasts 鉴定B-Raf诱导的人成纤维细胞衰老的细胞系统的建立
Pub Date : 2014-04-30 DOI: 10.26443/msurj.v9i1.159
Ran Shu
Background: B-Raf is one of the earliest and most common genetic mutations observed in many different types of cancers. A single mutation in B-Raf cannot cause full-blown cancer, but may cause an observed phenotype called oncogene induced senescence (OIS). This suggests the need for cooperation between B-Raf and other genes for successful tumorigenesis. Objective: We look to characterize Human Fibroblast cells that are able to senesce in response to elevated oncogenic expression of B-Raf. Methods: We introduced ectopic expression of inducible B-Raf into human fibroblast cells. We characterized the successfully infected cells based on their ability to induce senescence. Results: We isolated cells of clonal origin and we identified the clone most responsive to B-Raf expression. Conclusions and Future Research: Our methodology proved to be effective in creating a model of B-Raf expression that can be used to study OIS. The next step is to screen the cells to identify genes that enable the cells to evade senescence. These genes could prove to be valuable chemotherapeutic targets.
背景:B-Raf是在许多不同类型的癌症中发现的最早和最常见的基因突变之一。B-Raf的单一突变不能导致全面的癌症,但可能导致一种被称为癌基因诱导衰老(OIS)的观察到的表型。这表明需要B-Raf和其他基因之间的合作才能成功发生肿瘤。目的:我们希望表征人类成纤维细胞在B-Raf致癌表达升高时能够衰老的特性。方法:将诱导型B-Raf异位表达引入人成纤维细胞。我们根据诱导衰老的能力对成功感染的细胞进行了表征。结果:我们分离到克隆来源的细胞,并鉴定出对B-Raf表达最敏感的克隆。结论和未来研究:我们的方法被证明是有效的,可以创建一个可用于研究OIS的B-Raf表达模型。下一步是筛选细胞,以确定使细胞避免衰老的基因。这些基因可能被证明是有价值的化疗靶点。
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引用次数: 0
期刊
McGill Science undergraduate research journal : MSURJ
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