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Visualizing traumatic brain injury:ocular clues for diagnosis and assessment 被引量:1
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作者 Morteza Abyadeh Vivek Gupta +2 位作者 Yuyi You Joao A.Paulo Mehdi Mirzaei 《Neural Regeneration Research》 SCIE CAS 2025年第5期1399-1400,共2页
Traumatic brain injury (TBI) is defined as damage to the brain resulting from an external sudden physical force or shock to the head.It is considered a silent public health epidemic causing significant death and disab... Traumatic brain injury (TBI) is defined as damage to the brain resulting from an external sudden physical force or shock to the head.It is considered a silent public health epidemic causing significant death and disability globally.There were 64,000 TBI related deaths reported in the USA in 2020,with about US$76 billion in direct and indirect medical costs annually. 展开更多
关键词 DIAGNOSIS OCULAR INJURY
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Amyloid-beta and tau protein beyond Alzheimer's disease 被引量:16
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作者 Morteza Abyadeh Vivek Gupta +11 位作者 Joao A.Paulo Arezoo Gohari Mahmoudabad Sina Shadfar Shahab Mirshahvaladi Veer Gupta Christine T.O.Nguyen David I.Finkelstein Yuyi You Paul A.Haynes Ghasem H.Salekdeh Stuart L.Graham Mehdi Mirzaei 《Neural Regeneration Research》 SCIE CAS CSCD 2024年第6期1262-1276,共15页
The aggregation of amyloid-beta peptide and tau protein dysregulation are implicated to play key roles in Alzheimer's disease pathogenesis and are considered the main pathological hallmarks of this devastating dis... The aggregation of amyloid-beta peptide and tau protein dysregulation are implicated to play key roles in Alzheimer's disease pathogenesis and are considered the main pathological hallmarks of this devastating disease.Physiologically,these two proteins are produced and expressed within the normal human body.However,under pathological conditions,abnormal expression,posttranslational modifications,conformational changes,and truncation can make these proteins prone to aggregation,triggering specific disease-related cascades.Recent studies have indicated associations between aberrant behavior of amyloid-beta and tau proteins and various neurological diseases,such as Alzheimer's disease,Parkinson's disease,and amyotrophic lateral sclerosis,as well as retinal neurodegenerative diseases like Glaucoma and age-related macular degeneration.Additionally,these proteins have been linked to cardiovascular disease,cancer,traumatic brain injury,and diabetes,which are all leading causes of morbidity and mortality.In this comprehensive review,we provide an overview of the connections between amyloid-beta and tau proteins and a spectrum of disorders. 展开更多
关键词 AMYLOID-BETA cancer cardiovascular diseases DIABETES NEURODEGENERATION TAU traumatic brain injury
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人脐带间充质干细胞体外分化成骨细胞的研究 被引量:7
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作者 刘忠 李素萍 +6 位作者 杨宏友 王震 吕蓉 吴炳 方勤 李敏 吴学忠 《中国输血杂志》 CAS CSCD 北大核心 2011年第5期376-382,共7页
目的探讨人脐带源间充质干细胞(HUC-MSCs)定向诱导分化为成骨细胞的能力。方法人脐带经胶原酶和胰蛋白酶消化后于DMEM/F12培养基中培养,通过传代作纯化和扩增;采用倒置显微镜及电镜观察细胞形态,细胞计数绘制细胞生长曲线,流式细胞仪检... 目的探讨人脐带源间充质干细胞(HUC-MSCs)定向诱导分化为成骨细胞的能力。方法人脐带经胶原酶和胰蛋白酶消化后于DMEM/F12培养基中培养,通过传代作纯化和扩增;采用倒置显微镜及电镜观察细胞形态,细胞计数绘制细胞生长曲线,流式细胞仪检测细胞免疫表型及细胞周期;以含有成骨细胞诱导剂(地塞米松、β-甘油磷酸钠、抗坏血酸)的DMEM/F12培养基对传至第3代的细胞定向诱导分化为成骨细胞,并对诱导后细胞作成骨细胞检测。结果经酶消化后,细胞贴壁生长,主要呈"成纤维样",但体积较大、形状不规则、细胞质突起多,细胞核大而疏松,核仁明显;第1、3、5、7代细胞生长曲线基本相同;细胞表面表达CD105、CD90、CD44、CD29及CD13,不表达CD34、CD45、HLA-DR;培养至第4代的细胞约72.724%的细胞处G1期、S期的细胞仅占18.069%,第6代时G1期细胞约为83.875%、S期为9.606%左右;细胞经成骨细胞诱导分化后,细胞形态发生改变,线粒体明显增多,出现较多的基质小泡、髓样体和空泡状结构,碱性磷酸酶染色显示呈强阳性,茜苏红染色和Von-Kossa染色显示细胞有钙盐沉积并形成钙结节。结论人脐带中分离及培养扩增细胞具有MSCs的基本特性,具有分化为成骨细胞的能力。 展开更多
关键词 间充质干细胞 人脐带 体外培养 细胞周期 生长曲线 成骨细胞
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体外纯化培养外周血来源的树突状细胞的研究 被引量:3
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作者 李素萍 刘忠 +5 位作者 杨宏友 吕蓉 方勤 李敏 赵刚 王震 《中国输血杂志》 CAS CSCD 2008年第10期767-770,共4页
目的建立来源于外周血的树突状细胞(DCs)的纯化培养方法并观察DCs的形态及功能。方法以Fi-coll密度梯度离心法从正常人外周血中分离出外周血单个核细胞(PBMNC)后,用体外培养的手段,采用培养黏附法或经免疫磁珠筛选法,获得单核细胞;分别... 目的建立来源于外周血的树突状细胞(DCs)的纯化培养方法并观察DCs的形态及功能。方法以Fi-coll密度梯度离心法从正常人外周血中分离出外周血单个核细胞(PBMNC)后,用体外培养的手段,采用培养黏附法或经免疫磁珠筛选法,获得单核细胞;分别加入不同浓度的细胞因子(重组人粒细胞-巨噬细胞集落刺激因子重组人白介素4重组人肿瘤坏死因子α)诱导培养,培养12 d诱导出DCs;用光镜和电镜观察培养的DCs,用流式细胞仪检测DCs表面的细胞表型(CD80、CD83、CD86、CD1α、HLA-DR),MTT法检测DC对T细胞的刺激增殖效应。结果在体外诱导出外周血来源的成熟DCs,电镜和光镜分析表明具有DCs的典型形态,所培养的细胞表面高表达CD80、CD83、CD86、CD1α、HLA-DR,并具有刺激异基因淋巴细胞增殖的能力。结论应用外周血来源的单个核细胞,采用培养黏附法或免疫磁珠分选法分选出的单核细胞,细胞因子培养12 d可得到成熟正常的DCs。 展开更多
关键词 树突状细胞 粒细胞-巨噬细胞集落刺激因子 肿瘤坏死因子-Α 白细胞介素-4
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人外周血树突状细胞低温保存的优化研究 被引量:1
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作者 李素萍 杨宏友 +5 位作者 王震 吕蓉 郭晓婕 方勤 李敏 刘忠 《中国输血杂志》 CAS CSCD 北大核心 2011年第3期206-210,共5页
目的探寻冻存树突状细胞(DCs)优化的冷冻保护剂组合。方法配制含不同浓度二甲基亚砜(DM-SO)的3种冷冻保护剂组合,A组:5%DMSO+6%羟乙基淀粉(HES)+4%人血清白蛋白(HAS);B组:10%DMSO+40%FCS;C组:12%DMSO+40%FCS,比较3组冷冻保护剂对人外周... 目的探寻冻存树突状细胞(DCs)优化的冷冻保护剂组合。方法配制含不同浓度二甲基亚砜(DM-SO)的3种冷冻保护剂组合,A组:5%DMSO+6%羟乙基淀粉(HES)+4%人血清白蛋白(HAS);B组:10%DMSO+40%FCS;C组:12%DMSO+40%FCS,比较3组冷冻保护剂对人外周血CD14+单个核细胞诱导产生的成熟树突状细胞(mDCs)的冻存效果:采用两步法将mDCs冻存于-80℃冰箱过夜后转移至-196℃液氮气相中放置24 h,再将冻存的mDCs复苏后继续培养,并检测、比较冻存前后DC的形态、存活率、细胞表型及其对同种异体T细胞刺激活性的差异。结果 3组不同组合冷冻保护剂冷冻保存的mDCs复苏后其存活的细胞的形态没有发生明显改变,仍保留其成熟表型,并具备对T细胞的刺激活性。结论 3种不同浓度的DMSO冷冻保存mDCs,5%DMSO+6%HES+4%HSA组合更适宜。 展开更多
关键词 树突状细胞 人外周血 冷冻保存 CD14^+ 单个核细胞 混合淋巴细胞反应
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负载卵巢癌冻融抗原对树突状细胞分泌细胞因子的影响
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作者 李素萍 杨宏友 +5 位作者 王震 吕蓉 方勤 赵刚 李敏 刘忠 《临床输血与检验》 CAS 2009年第3期193-198,共6页
目的探讨负载卵巢癌冻融抗原对树突状细胞分泌细胞因子的影响。方法采用反复冻融法获得卵巢癌细胞株SKOV3细胞抗原,联合应用重组人粒细胞-巨噬细胞集落刺激因子、重组人白细胞介素-4和重组人肿瘤坏死因子-α,体外诱导人外周血CD14+单核... 目的探讨负载卵巢癌冻融抗原对树突状细胞分泌细胞因子的影响。方法采用反复冻融法获得卵巢癌细胞株SKOV3细胞抗原,联合应用重组人粒细胞-巨噬细胞集落刺激因子、重组人白细胞介素-4和重组人肿瘤坏死因子-α,体外诱导人外周血CD14+单核细胞为成熟DCs并负载卵巢癌肿瘤抗原;采用ELISA法检测培养细胞上清液中分泌IL-12p70、IFN-γ和IL-10含量,评价非成熟DCs和成熟DCs以及肿瘤抗原负载DCs和未负载肿瘤抗原DCs激活的CTL分泌细胞因子的能力。结果联合应用重组人的GM-CSF、IL-4和TNF-α可在体外诱导出成熟DCs;经ELISA方法检测,不同状态下的DCs分泌IL-12p70、IFN-γ的量不同,成熟DCs较非成熟DCs有更强的分泌IL-12p70、IFN-γ的能力(P<0.05),负载抗原DCs激活的CTL较未负载抗原DCs激活的CTL有更强的分泌IL-12p70[(182.89±4.57)pg/ml和(99.76±5.42)pg/ml,P<0.01]和IFN-γ的能力[(102.11±5.95)pg/ml和(68.29±5.04)pg/ml,P<0.01]。而成熟DCs分泌IL-10的能力与非成熟DCs相比,差异无统计学意义(P>0.05)。负载抗原后DCs激活的CTL与未负载抗原DCs激活CTL上清液中IL-10的浓度相比,两者之间的差异无统计学意义(P>0.05)。结论细胞因子的分泌量受DCs的成熟状态及某些刺激信号的影响,卵巢癌冻融抗原是其刺激信号之一。 展开更多
关键词 树突状细胞 细胞因子 卵巢癌 冻融抗原
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人脐带源间充质干细胞临床输注前的优化制备 被引量:1
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作者 李素萍 杨宏友 +5 位作者 王震 吕蓉 郭晓婕 王超 邢昕 刘忠 《中国输血杂志》 CAS CSCD 北大核心 2012年第11期1160-1164,共5页
目的探讨人脐带源间充质干细胞(HUC-MSCs)临床输注前制备成细胞悬液,细胞活性和细胞表面抗原的变化。方法第3~5代人脐带源间充质干细胞用0.25%胰蛋白酶消化处理,PBS洗涤5次,分别重悬于磷酸盐缓冲液(PBS)或含有50 U/ml肝素-PBS、100 U/m... 目的探讨人脐带源间充质干细胞(HUC-MSCs)临床输注前制备成细胞悬液,细胞活性和细胞表面抗原的变化。方法第3~5代人脐带源间充质干细胞用0.25%胰蛋白酶消化处理,PBS洗涤5次,分别重悬于磷酸盐缓冲液(PBS)或含有50 U/ml肝素-PBS、100 U/ml肝素-PBS、200 U/ml肝素-PBS中,放置于4℃、22℃或37℃条件下,分别延长至1 h、2 h、3 h,检测细胞存活率和细胞表面抗原的变化。结果 HUC-MSCs收集后重悬于PBS中,在4℃条件下,随着在体外放置时间的延长,细胞的存活率在随之下降,但细胞存活率明显高于放置22℃、37℃条件下的细胞。将细胞收集后重悬于含有肝素的PBS溶液中,细胞既无聚集现象,而且随着肝素浓度的增加,细胞的存活率相对较高,体外短暂保存HUC-MSCs的效果较好。在含200 U/ml肝素的PBS溶液中,4℃条件下细胞放置3 h后经苔盼兰染色镜下计数可知,HUC-MSCs存活率可维持在(91.3±3.08)%,而且HUC-MSCs表面仍高表达CD105、CD73、CD44、CD90。结论临床输注前制备HUC-MSCs重悬于含200 U/ml肝素-PBS中在4℃条件下3 h内可供临床有效输注。 展开更多
关键词 间充质干细胞 肝素 细胞活性 临床输注
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Potential Breeding for High Nitrogen Fixation in <i>Pisum sativum</i>L.: Germplasm Phenotypic Characterization and Genetic Investigation 被引量:3
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作者 R. Abi-Ghanem E. T. Bodah +1 位作者 M. Wood K. Braunwart 《American Journal of Plant Sciences》 2013年第8期1597-1600,共4页
Nitrogen (N) is the most yield-limiting crop nutrient worldwide. Industrially produced N has increased in cost over the past years, and is unavailable in many regions around the globe. Biological N fixation by rhizobi... Nitrogen (N) is the most yield-limiting crop nutrient worldwide. Industrially produced N has increased in cost over the past years, and is unavailable in many regions around the globe. Biological N fixation by rhizobial bacteria is a great underutilized resource that this project aims to maximize. Grain legumes fix approximately 20 to 100 kg·N·ha-1·yr-1. The amount of N supplied by fixation is affected by genes and traits of both the bacterial and plant partners. The objectives of this study are to identify Pisum sativum varieties with high nitrogen fixation efficiency. This is achieved by germplasm screening and phenotypic evaluation of nodule formation, total plant nitrogen, and residual nitrogen in soil. Significant differences in plant total nitrogen among the various cultivated genotypes were found, with heritability of 0.57. These pea varieties left in the soil a residual N that varies between 11.21 to 65.018 kg.N.ha-1. Our findings reveal a unique opportunity for improving N fixation through genetic crossing and selection. 展开更多
关键词 Nitrogen FIXATION Field PEAS Agricultural INPUTS
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Single Nucleotide Polymorphism-Based Chromosomal Microarray Evaluation of Hydatidiform Moles: A US National Reference Laboratory Experience
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作者 Arturo Anguiano Boris T. Wang +4 位作者 Kylin Y. Lammers Loretta W. Mahon Nicole Truitt Lindsay Dohany Fatih Z. Boyar 《Open Journal of Obstetrics and Gynecology》 2020年第8期1122-1134,共13页
<strong>Objectives</strong>:<span> This retrospective study evaluated 1) benefits of single nucleotide polymorphism (SNP)-based chromosomal microarrays (CMAs) in the diagnosis of complete hydatidifor... <strong>Objectives</strong>:<span> This retrospective study evaluated 1) benefits of single nucleotide polymorphism (SNP)-based chromosomal microarrays (CMAs) in the diagnosis of complete hydatidiform mole (CHM) and partial HM (PHM) in products of conception (POC) and amniotic fluid (AF) specimens, and 2) frequency of whole-genome uniparental disomy (wgUPD) and triploidy in POC and AF specimens received at a US national reference laboratory.</span><span "=""> </span><b><span>Methods:</span></b><span> We reviewed consecutive 2138 POC and 3230 AF specimens and identified the cases with wgUPD and triploidy which are associated with molar pregnancy.</span><span "=""> </span><b><span>Results:</span></b><span "=""><span> Of 2138 consecutive POC specimens tested, SNP-based CMA detected wgUPD in 10 (0.47%) and triploidy in 84 (3.93%). Of the 10 wgUPD cases, 9 (90%) were confirmed as CHM. Of 3230 consecutive AF specimens, the array detected wgUPD in 1 case (0.03%) and triploidy in 11 (0.34%). </span><b><span>Conclusions:</span></b><span> SNP-based microarray allows detection of wgUPD in POC and AF specimens at a US national reference laboratory. Correctly diagnosing HM and differentiating CHM from PHM </span></span><span>are</span><span> important for clinical management. The effective SNP-based CMA detection of wgUPD in CHM may enable physicians to monitor patients at risk for gestational trophoblastic disease and neoplasm.</span><span "=""> </span><span "=""><span>Conventional chromosome analysis of POC has a high </span><span>failure rate, cannot be performed on formalin-fixed paraffin embedded samples, and cannot detect wgUPD. Further</span></span><span "=""> </span><span>multi-institutional collaborative assessmen</span><span> on accuracy, cost-effectiveness, and adequate access to SNP-based CMA, may lead this testing platform to be considered as the first-tier analysis tool for POC specimens, including those showing PHM or CHM. 展开更多
关键词 Complete Hydatidiform Mole (CHM) Gestational Trophoblastic Disease (GTD) Gestational Trophoblastic Neoplasm (GTN) Partial Hydatidiform Mole (PHM) TRIPLOIDY Whole Genome Uniparental Disomy (wgUPD)
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SYNCRIP promotes cell cycle progression and lung tumorigenesis by modulating AURKB translation
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作者 Hyeon Ji Kim Hye Guk Ryu +10 位作者 Mingyu Kang Namgyu Lee Hyo-Jin Kim Dahye Lee Chaeuk Chung Sangjune Kim Kyung-Ha Lee Wanil Kim Jin-Seok Byun Kyong-Tai Kim Do-Yeon Kim 《Cancer Communications》 2025年第2期138-142,共5页
Dysregulation of cellular processes,such as cell division and proliferation,is a hallmark of cancer and is driven by the aberrant expression of cell cyclerelated genes[1].Aurora kinase B(AURKB),due to its pivotal role... Dysregulation of cellular processes,such as cell division and proliferation,is a hallmark of cancer and is driven by the aberrant expression of cell cyclerelated genes[1].Aurora kinase B(AURKB),due to its pivotal role in mitotic progression,has been implicated in various cancers.Overexpression or hyperactivation of AURKB significantly contributes to tumorigenesis and cancer progression[2].Although mechanisms that enhance AURKB activity,including binding to INCENP,autophosphorylation[3],and ubiquitination by TRAF6[4],have been extensively investigated,regulation of AURKB synthesis,particularly mRNA translation,remains unclear.The translation of eukaryotic mRNAs typically occurs either through cap-dependent scanning or through direct ribosomal binding to specialized RNA elements known as internal ribosome entry sites(IRES).IRES-mediated translation is strongly influenced by specific RNA-binding proteins,known as IRES trans-acting factors(ITAFs).SYNCRIP(Synaptotagmin-binding cytoplasmic RNA-interacting protein),also known as hnRNP Q,has been identified as an ITAF[5],integrating various aspects of RNA metabolism with key cellular processes.Here,we aim to elucidate the mechanism of AURKB mRNA translation and investigate whether SYNCRIP regulates AURKB mRNA translation in lung cancer. 展开更多
关键词 TRANSLATION HAS SUCH
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