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Predicting intrinsic disorder in proteins: an overview 被引量:11
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作者 Bo He Kejun Wang +3 位作者 Yunlong Liu Bin Xue Vladimir N Uversky A Keith Dunker 《Cell Research》 SCIE CAS CSCD 2009年第8期929-949,共21页
The discovery of intrinsically disordered proteins (IDP) (i.e., biologically active proteins that do not possess stable secondary and/or tertiary structures) came as an unexpected surprise, as the existence of suc... The discovery of intrinsically disordered proteins (IDP) (i.e., biologically active proteins that do not possess stable secondary and/or tertiary structures) came as an unexpected surprise, as the existence of such proteins is in contradiction to the traditional "sequence →structure →function" paradigm. Accurate prediction of a protein's predisposition to be intrinsically disordered is a necessary prerequisite for the further understanding of principles and mechanisms of protein folding and function, and is a key for the elaboration of a new structural and functional hierarchy of proteins. Therefore, prediction of IDPs has attracted the attention of many researchers, and a number of prediction tools have been developed. Predictions of disorder, in turn, are playing major roles in directing laboratory experiments that are leading to the discovery of ever more disordered proteins, and thereby leading to a positive feedback loop in the investigation of these proteins. In this review of algorithms for intrinsic disorder prediction, the basic concepts of various prediction methods for IDPs are summarized, the strengths and shortcomings of many of the methods are analyzed, and the difficulties and directions of future development of IDP prediction techniques are discussed. 展开更多
关键词 protein intrinsic disorder prediction method
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Water relations and an expression analysis of plasma membrane intrinsic proteins in sensitive and tolerant rice during chilling and recovery 被引量:11
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作者 Xin Yu Yan Hui Peng +3 位作者 Min Hua Zhang Yan Jun Shao Wei Ai Su Zhang Cheng Tang 《Cell Research》 SCIE CAS CSCD 2006年第6期599-608,共10页
A symptom of chilling injury is development of water deficit in shoots, resulting from an imbalance of water transport and transpiration. In this work, two rice varieties (Oryza sativa L. var. Wasetoitsu and Somewake... A symptom of chilling injury is development of water deficit in shoots, resulting from an imbalance of water transport and transpiration. In this work, two rice varieties (Oryza sativa L. var. Wasetoitsu and Somewake) seedlings were chilled at 7 ℃, followed by recovery at 28 ℃. Based on the growth phenotype and electrolyte leakage tests, Somewake was shown to be a chilling-tolerant variety, and Wasetoitsu a chilling-sensitive one. The chilling stress reduced markedly the relative water content (RWC) of leaves, accumulative transpiration and osmotic root hydraulic conductivity (Lp) in both varieties. But when retumed to 28 ℃, the water relation balance of Somewake recovered better. The mRNA expression profile of all the 11 plasma membrane intrinsic proteins (PIPs), a subgroup of aquaporins, was subsequently determined by real-time reverse transcription (RT)-PCR with TaqMan-minor grove binder (MGB) probes derived from rice var. Nipponbare during chilling treatment and recovery. Most of the PIP genes was down-regulated at the low temperature, and recovered at the warm temperature. The relative expression of some PIPs in both Somewake and Wasetoitsu decreased in parallel during the chilling. However during the recovery, the relative expression of OsPIP1;1, OsPIP2;1, OsPIP2;7 in shoots and OsPIP1:1, OsPIP2:1 in roots were significantly higher in Somewake than Wasetoitsu. This supports the role of PIPs in re-establishing water balance after chilling conditions. We discuss the diversified roles played by members of the aquaporin PIP subfamily in plant chilling tolerance depending on aquaporin isoforms, plant tissue and the stage of chilling duration. 展开更多
关键词 AQUAPORIN CHILLING gene expression plasma membrane intrinsic protein RICE
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Prediction of Intrinsically Disordered Proteins with a Low Computational Complexity Method 被引量:1
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作者 Jia Yang Haiyuan Liu Hao He 《Computer Modeling in Engineering & Sciences》 SCIE EI 2020年第10期111-123,共13页
The prediction of intrinsically disordered proteins is a hot research area in bio-information.Due to the high cost of experimental methods to evaluate disordered regions of protein sequences,it is becoming increasingl... The prediction of intrinsically disordered proteins is a hot research area in bio-information.Due to the high cost of experimental methods to evaluate disordered regions of protein sequences,it is becoming increasingly important to predict those regions through computational methods.In this paper,we developed a novel scheme by employing sequence complexity to calculate six features for each residue of a protein sequence,which includes the Shannon entropy,the topological entropy,the sample entropy and three amino acid preferences including Remark 465,Deleage/Roux,and Bfactor(2STD).Particularly,we introduced the sample entropy for calculating time series complexity by mapping the amino acid sequence to a time series of 0-9.To our knowledge,the sample entropy has not been previously used for predicting IDPs and hence is being used for the first time in our study.In addition,the scheme used a properly sized sliding window in every protein sequence which greatly improved the prediction performance.Finally,we used seven machine learning algorithms and tested with 10-fold cross-validation to get the results on the dataset R80 collected by Yang et al.and of the dataset DIS1556 from the Database of Protein Disorder(DisProt)(https://www.disprot.org)containing experimentally determined intrinsically disordered proteins(IDPs).The results showed that k-Nearest Neighbor was more appropriate and an overall prediction accuracy of 92%.Furthermore,our method just used six features and hence required lower computational complexity. 展开更多
关键词 BIOINFORMATICS intrinsically disordered proteins machine learning algorithms SEQUENCES computational complexity
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Prediction of Intrinsically Disordered Proteins Based on Deep Neural Network-ResNet18 被引量:1
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作者 Jie Zhang Jiaxiang Zhao Pengchang Xu 《Computer Modeling in Engineering & Sciences》 SCIE EI 2022年第5期905-917,共13页
Accurately,reliably and rapidly identifying intrinsically disordered(IDPs)proteins is essential as they often play important roles in various human diseases;moreover,they are related to numerous important biological a... Accurately,reliably and rapidly identifying intrinsically disordered(IDPs)proteins is essential as they often play important roles in various human diseases;moreover,they are related to numerous important biological activities.However,current computational methods have yet to develop a network that is sufficiently deep tomake predictions about IDPs and demonstrate an improvement in performance.During this study,we constructed a deep neural network that consisted of five identical variant models,ResNet18,combined with an MLP network,for classification.Resnet18 was applied for the first time as a deep model for predicting IDPs,which allowed the extraction of information fromIDP residues in greater detail and depth,and this information was then passed through the MLP network for the final identification process.Two well-known datasets,MXD494 and R80,were used as the blind independent datasets to compare their performance with that of our method.The simulation results showed that Matthew’s correlation coefficient obtained using our deep network model was 0.517 on the blind R80 dataset and 0.450 on the MXD494 dataset;thus,our method outperformed existing methods. 展开更多
关键词 ResNet18 MLP intrinsically disordered protein
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Nodulin 26-like intrinsic protein Cs NIP2;2 is a silicon influx transporter in Cucumis sativus L.
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作者 DUAN Yao-ke SU Yan +2 位作者 HAN Rong SUN Hao GONG Hai-jun 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2022年第3期685-696,共12页
Nodulin 26-like intrinsic proteins(NIPs) are a family of channel-forming transmembrane proteins that function in the transport of water and other small molecules.Some NIPs can mediate silicon transport across plasma m... Nodulin 26-like intrinsic proteins(NIPs) are a family of channel-forming transmembrane proteins that function in the transport of water and other small molecules.Some NIPs can mediate silicon transport across plasma membranes and lead to silicon accumulation in plants,which is beneficial for the growth and development of plants.Cucumber is one of the most widely consumed vegetables;however,the functions of NIPs in this crop are still largely unknown.Here,we report the functional characteristics of Cs NIP2;2.It was found that Cs NIP2;2 is a tandem repeat of Cs NIP2;1,which had been demonstrated to be a silicon influx transporter gene.Cs NIP2;2 has a selectivity filter composed of cysteine,serine,glycine and arginine(CSGR),which is different from all previously characterized silicon influx transporters in higher plants at the second helix position.Xenopus laevis oocytes injected with Cs NIP2;2 c RNA demonstrated a higher uptake of silicon than the control,and the uptake remained unchanged under low temperature.Cs NIP2;2 was found to be expressed in the root,stem,lamina and petiole,and exogenous silicon treatment decreased its expression in the stem but not in other tissues.Transient expression of Cs NIP2;2-e GFP fusion sequence in onion epidermal cells showed that Cs NIP2;2 was localized to the cell nucleus,plasma membrane and an unknown structure inside the cell.The results suggest that Cs NIP2;2 is a silicon influx transporter in cucumber,and its subcellular localization and the selectivity filter are different from those of the previously characterized silicon influx transporters in other plants.These findings may be helpful for understanding the functions of NIPs in cucumber plants. 展开更多
关键词 cucumber(Cucumis sativus L.) nodulin 26-like intrinsic membrane protein(NIP) silicon influx transporter aromatic/arginine selectivity filter
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Change of Water-Soluble-Protein, Urea-Soluble-Protein and Membrane Intrinsic Protein in Human Senile Cataract
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作者 HuirenZhao JianhuaYang 《眼科学报》 1995年第3期124-127,共4页
Purpose:To analyze the change of water-soluble-protein(WSP),urea-soluble-protein(USP)and membrane intrinsic protein(MIP)in human senile catarct.Methods:The water-soluble-fractions(WSF)were prepared basically according... Purpose:To analyze the change of water-soluble-protein(WSP),urea-soluble-protein(USP)and membrane intrinsic protein(MIP)in human senile catarct.Methods:The water-soluble-fractions(WSF)were prepared basically according to the method of Kibbelear,et al.But in this study,5mmol/LB-mercaptoethanol was added to the buffer solution.The urea-soluble-fractions(USF)were pre-pared basically according to the method of Kibbelear,et al.Lens fiber cell mem-branes were purified basically according to the method of Russell,et al.SDS-PAGE were performed according to the procedure of Laemmili,et al.using re-solving gel13%and3%stacking gel.Results:The WSPwas fractionated intoHM^+α^-,β1-3^-andγ-crystallin compo-nents.In nuclear cataractous lenses HM^+α^-and B-crystallin increase,while r-crystallin decrease.The USP from clear lenses contains mainlyαβchains of22KD,whereas in cataractous lenses,especially in nuclear cataractous lenses,the relative amount of the 28-and23KDpolypeptide(the components of β-crys-tallin)increased markedly.Lens fiber cell MIP,clear lens and cataract lens con-tained the main polypeptide of 27KD(MIP)and23KD(MP23).Conclusion:The water-insolube protein,whether in quantity or in quality,plays an important role in cataract formation.Eye Science 1995,11:124-127. 展开更多
关键词 白内障 老年人 WSP USP mip 发病机制
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Novel MIP gene mutation causes autosomal-dominant congenital cataract
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作者 Jing-Lan Ni Hua-Ming Wen +4 位作者 Xiao-Sheng Huang Qian-Wen Li Jia-Min Cai Bao-Jian Fan Jun Zhao 《International Journal of Ophthalmology(English edition)》 SCIE CAS 2024年第3期454-465,共12页
●AIM:To identify disease-causative mutations in families with congenital cataract.●METHODS:Two Chinese families with autosomaldominant congenital cataract(ADCC)were recruited and underwent comprehensive eye examinat... ●AIM:To identify disease-causative mutations in families with congenital cataract.●METHODS:Two Chinese families with autosomaldominant congenital cataract(ADCC)were recruited and underwent comprehensive eye examinations.Gene panel next-generation sequencing of common pathogenic genes of congenital cataract was performed in the proband of each family.Sanger sequencing was used to valid the candidate gene mutations and sequence the other family members for co-segregation analysis.The effect of sequence changes on protein structure and function was predicted through bioinformatics analysis.Major intrinsic protein(MIP)-wildtype and MIP-G29R plasmids were constructed and microinjected into zebrafish single-cell stage embryos.Zebrafish embryonic lens phenotypes were screened using confocal microscopy.●RESULTS:A novel heterozygous mutation(c.85G>A;p.G29R)in the MIP gene was identified in the proband of one family.A known heterozygous mutation(c.97C>T;p.R33C;rs864309693)in MIP was found in the proband of another family.In-silico prediction indicated that the novel mutation might affect the MIP protein function.Zebrafish embryonic lens was uniformly transparent in both wild-type PCS2+MIP and mutant PCS2+MIP.●CONCLUSION:Two missense mutations in the MIP gene in Chinese cataract families are identified,and one of which is novel.These findings expand the genetic spectrum of MIP mutations associated with cataracts.The functional studies suggest that the novel MIP mutation might not be a gain-of-function but a loss-of-function mutation. 展开更多
关键词 congenital cataract major intrinsic protein missense mutation zebrafish model
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抗沙眼衣原体MIP蛋白单克隆抗体的制备及特性鉴定 被引量:4
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作者 陆春雪 彭波 +4 位作者 陈超群 周洲 彭江南 钟光明 吴移谋 《中国免疫学杂志》 CAS CSCD 北大核心 2014年第1期80-84,共5页
目的:制备小鼠抗沙眼衣原体MIP蛋白单克隆抗体并鉴定其生物学特性。方法:重组MIP蛋白免疫BALB/c小鼠,取小鼠脾细胞与SP2/0骨髓瘤细胞进行常规融合,间接ELISA法筛选阳性克隆并进行有限稀释克隆化,建立分泌抗MIP蛋白单克隆抗体的杂交瘤细... 目的:制备小鼠抗沙眼衣原体MIP蛋白单克隆抗体并鉴定其生物学特性。方法:重组MIP蛋白免疫BALB/c小鼠,取小鼠脾细胞与SP2/0骨髓瘤细胞进行常规融合,间接ELISA法筛选阳性克隆并进行有限稀释克隆化,建立分泌抗MIP蛋白单克隆抗体的杂交瘤细胞株,进一步采用ELISA法鉴定单克隆抗体的效价、类别及抗MIP蛋白特异性,IFA法鉴定单克隆抗体的衣原体种属特异性及中和能力。结果:建立了2株能稳定分泌抗MIP蛋白单克隆抗体的杂交瘤细胞株(1R6H6、2L9D2),ELISA法测得培养上清效价均为1:1 600,免疫球蛋白类型分别为IgG2a和IgG1;2株单克隆抗体不仅能特异性的识别MIP重组蛋白,而且能特异性识别沙眼衣原体血清型A、D、L2所编码的内源性MIP蛋白,但不识别其他衣原体优势蛋白及MoPn、AR39和6BC;体外中和试验表明,2株单克隆抗体均能有效中和衣原体的感染性。结论:获得了有活性的能特异性识别MIP蛋白的单克隆抗体,为深入研究MIP蛋白的结构和功能奠定了基础。 展开更多
关键词 沙眼衣原体 mip蛋白 单克隆抗体 鉴定
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MIP-2、MIP-1α和IL-6在小鼠血流感染中的变化规律实验研究 被引量:6
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作者 徐舒敏 谢尹晶 +4 位作者 郭宇妮 陈文燕 李芮冰 王正冠 王成彬 《北京医学》 CAS 2015年第1期37-40,F0003,共5页
目的探讨巨噬细胞炎性蛋白2(macrophage inflammatory protein-2,MIP-2)、巨噬细胞炎性蛋白1α(macrophage inflammatory protein-1 Alpha,MIP-1α)和白细胞介素6(interleukin-6,IL-6)在金黄色葡萄球菌和大肠埃希菌感染时的变化规律及... 目的探讨巨噬细胞炎性蛋白2(macrophage inflammatory protein-2,MIP-2)、巨噬细胞炎性蛋白1α(macrophage inflammatory protein-1 Alpha,MIP-1α)和白细胞介素6(interleukin-6,IL-6)在金黄色葡萄球菌和大肠埃希菌感染时的变化规律及在鉴别诊断金黄色葡萄球菌和大肠埃希菌感染的价值。方法将216只ICR小鼠随机分为3组,各组72只。尾静脉注射大肠埃希菌和金黄色葡萄球菌建立小鼠血流感染模型,生理盐水注射建立阴性对照。共9个时间点,各时间点每组8只小鼠。分别在感染0.5 h、1 h、3 h、6 h、12 h、1 d、2 d、3 d、5 d后采血,检测血液白细胞计数(WBC),血清中MIP-2、MIP-1α和IL-6浓度。结果 1大肠埃希菌组和金黄色葡萄球菌组小鼠在感染0.5 h后MIP-2、MIP-1α和IL-6均明显升高,各指标峰值分别为(13 246.8±865.37)pg/ml、(699.79±36.36)pg/ml、(25 080.32±1 263.58)pg/ml、(3 483.22±169.84)pg/ml和(1 171.98±104.49)pg/ml、(94.71±14.38)pg/ml,大肠埃希菌感染组显著高于金黄色葡萄球菌感染组;2MIP-2、MIP-1α和IL-6在大肠埃希菌感染时的ROC曲线下面积(0.962、0.967、0.962)与金黄色葡萄球菌感染时的(0.877、0.889、0.885)的差异有统计学意义(P<0.05),并且两组之间差异也有统计学意义(P<0.05)。结论 MIP-2、MIP-1α和IL-6在炎症早期明显升高,在鉴别大肠埃希菌和金黄色葡萄球菌引发的感染均具有统计学意义。 展开更多
关键词 感染 巨噬细胞炎性蛋白2 巨噬细胞炎性蛋白1Α 白细胞介素6
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晶状体主要内源性蛋白MIP的突变体致先天性白内障的发生机制 被引量:3
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作者 胡姗姗 马笮 +2 位作者 赵保文 林辉 齐艳华 《眼科新进展》 CAS 北大核心 2015年第3期218-222,共5页
目的研究晶状体主要内源性蛋白(major intrinsic protein,MIP)R233K突变体的产生是否影响MIP与钙调蛋白的相互作用,继而阐述此突变致先天性白内障的发病机制。方法构建连有EGFP的MIP野生型及R233K突变体表达质粒,分别转染Hela细胞系,确... 目的研究晶状体主要内源性蛋白(major intrinsic protein,MIP)R233K突变体的产生是否影响MIP与钙调蛋白的相互作用,继而阐述此突变致先天性白内障的发病机制。方法构建连有EGFP的MIP野生型及R233K突变体表达质粒,分别转染Hela细胞系,确定R233K突变体的亚细胞定位。用免疫共沉淀技术来检测R233K突变体与钙调蛋白的相互作用。合成野生型及突变型MIP羧基末端多肽链,用荧光素报告基因技术来验证这些多肽链的功能。结果在EGFP的显影下,野生型及R233K突变体均定位于细胞膜上,p.R233K突变未影响MIP的亚细胞定位及其在细胞内的蛋白表达量。而免疫共沉淀实验显示,与野生型MIP相比,位于羧基末端的R233K突变体与钙调蛋白的相互作用明显减弱。荧光素报告基因实验证实,突变后的MIP与钙调蛋白的绑定亲和力明显下降。结论R233K突变体影响了MIP与钙调蛋白的相互作用,降低了MIP羧基末端与钙调蛋白的绑定亲和力,继而影响了晶状体纤维细胞的水通透性,导致了先天性白内障的发生。 展开更多
关键词 晶状体主要内源性蛋白 钙调蛋白 相互作用关系 机制
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Tuftsin衍生物TP影响肿瘤相关巨噬细胞MIP-1α分子表达 被引量:6
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作者 安映红 贾娜 +3 位作者 李琳娜 韩苏 杨德宣 袁守军 《中国药理学通报》 CAS CSCD 北大核心 2014年第10期1357-1361,共5页
目的探讨TP对肿瘤相关的趋化因子巨噬细胞炎性蛋白1-α(MIP-1α)表达的影响。方法使用RT-PCR的试验方法,检测小鼠巨噬细胞Ana-1细胞和肿瘤组织中提取的巨噬细胞中MIP-1α的表达;建立小鼠S180肉瘤细胞皮下移植瘤双瘤模型,待肿瘤体积生长... 目的探讨TP对肿瘤相关的趋化因子巨噬细胞炎性蛋白1-α(MIP-1α)表达的影响。方法使用RT-PCR的试验方法,检测小鼠巨噬细胞Ana-1细胞和肿瘤组织中提取的巨噬细胞中MIP-1α的表达;建立小鼠S180肉瘤细胞皮下移植瘤双瘤模型,待肿瘤体积生长至约250 mm3时,将其中一侧建立术后残瘤模型,并开始以8 mg·kg-1剂量的TP给药,隔天1次,给药4次后,分离肿瘤组织,免疫组化检测MIP-1α的表达。结果不同浓度TP对小鼠TAMs的MIP-1α表达较空白对照组明显减少,并呈剂量依赖性;体内试验中,TP处理组的荷瘤小鼠的肿瘤组织MIP-1α与对照组相比表达明显降低,接近于阳性药环磷酰胺组;但是MIP-1α在小鼠Ana-1细胞和TAMs中的mRNA表达量差异没有统计学意义;不同浓度TP对小鼠Ana-1细胞的MIP-1α表达差异也没有统计学意义。结论 TP不能影响小鼠Ana-1细胞系的MIP-1α表达,但TP对肿瘤组织中的巨噬细胞MIP-1α的表达有明显影响;MIP-1α有可能是TP抗癌作用机制的新靶点。 展开更多
关键词 免疫增强剂 T肽(TP) 巨噬细胞炎性蛋白1-α(mip-1α) 术后残瘤模型 肿瘤相关巨噬细胞(TAMs) 双瘤模型
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人趋化因子MIP-3α的原核可溶性表达及趋化活性分析 被引量:1
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作者 余相 刘瑞玉 刘集鸿 《中国生物工程杂志》 CAS CSCD 北大核心 2005年第11期66-70,共5页
目的:克隆人趋化因子MIP3α,进行原核表达并初步鉴定其趋化活性。方法:从人扁桃体中提取总RNA,进行RTPCR,扩增MIP3α成熟蛋白基因,重组于pET32a(+)载体,转化大肠杆菌BL21TrxB(DE3),进行融合表达,Westernblot验证融合蛋白,金属离子亲和层... 目的:克隆人趋化因子MIP3α,进行原核表达并初步鉴定其趋化活性。方法:从人扁桃体中提取总RNA,进行RTPCR,扩增MIP3α成熟蛋白基因,重组于pET32a(+)载体,转化大肠杆菌BL21TrxB(DE3),进行融合表达,Westernblot验证融合蛋白,金属离子亲和层析,肠激酶酶切,弱阳离子交换层析,得到纯化的MIP3α蛋白,趋化试验鉴定其趋化活性。结果:成功构建了MIP3α天然蛋白的硫氧还蛋白融合表达载体,表达并纯化出MIP3α蛋白,Westernblot证明融合蛋白能与羊抗人MIP3α抗体结合,纯化的MIP3α蛋白能趋化HEK293CCR6稳定转染细胞。结论:构建的天然MIP3α融合表达载体以可溶性蛋白的方式稳定表达MIP3α,初步纯化得到的MIP3α具有趋化HEK293CCR6稳定转染细胞的活性。 展开更多
关键词 mip-3Α 融合表达 蛋白纯化
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RANTES、MIP-1α、MIP-1β和MCP-1趋化因子在慢性肝病患者的水平 被引量:16
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作者 刘宁 江娜 +4 位作者 罗娜 乔桂芳 孙焕芹 刘金花 张永宏 《北京医学》 CAS 2014年第6期426-428,共3页
目的探讨慢性乙型肝炎(CHB)、乙肝肝硬化(LC)、乙肝相关肝细胞癌(HCC)患者体内正常T细胞表达和分泌调节活化因子(RANTES)、巨噬细胞炎症蛋白(MIP-1α和MIP-1β)和单核细胞趋化蛋白(MCP-1)的表达水平。方法收集2010年2月至2011年11月首... 目的探讨慢性乙型肝炎(CHB)、乙肝肝硬化(LC)、乙肝相关肝细胞癌(HCC)患者体内正常T细胞表达和分泌调节活化因子(RANTES)、巨噬细胞炎症蛋白(MIP-1α和MIP-1β)和单核细胞趋化蛋白(MCP-1)的表达水平。方法收集2010年2月至2011年11月首都医科大学附属北京佑安医院收治的CHB患者(40例)、LC患者(40例)、HCC患者(53例)的血液标本,采用Luminex技术检测血清趋化因子RANTES、MIP-1α、MIP-1β和MCP-1的表达水平,并以25例健康志愿者血液标本作为正常对照。结果趋化因子MIP-1α、MIP-1β和MCP-1在正常对照组表达水平的中位数分别为9.590、106.490和72.330 pg/ml,高于CHB组、LC组和HCC组;趋化因子RANTES在HCC组的表达水平为16 948.440 pg/ml,依次高于正常对照组、CHB组、LC组,差异有统计学意义(α<0.008)。结论趋化因子RANTES的表达水平与乙肝相关HCC的发生关系密切,可以作为HCC发生发展的辅助监测指标。 展开更多
关键词 慢性乙型肝炎 肝硬化 肝细胞癌 正常T细胞表达和分泌调节活化因子 巨噬细胞炎症蛋白 单核细胞趋化蛋白
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趋化因子MIP-1α和MCP-1及其受体CCR-1和CCR-2在慢性髓系白血病细胞中的表达 被引量:2
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作者 王伟良 沈悌 +2 位作者 惠玉荣 顾惜春 李蓉生 《中国实验血液学杂志》 CAS CSCD 2006年第3期433-436,共4页
本文旨在研究MIP-1α和MCP-1及其受体CCR-1和CCR-2在慢性髓系白血病细胞中的表达,同时观察P210bcr/abl融合蛋白中酪氨酸激酶对MIP-1α和MCP-1及其受体CCR-1和CCR-2mRNA表达的影响。在bcr/abl融合基因阴性和阳性慢性髓系白血病细胞中,采... 本文旨在研究MIP-1α和MCP-1及其受体CCR-1和CCR-2在慢性髓系白血病细胞中的表达,同时观察P210bcr/abl融合蛋白中酪氨酸激酶对MIP-1α和MCP-1及其受体CCR-1和CCR-2mRNA表达的影响。在bcr/abl融合基因阴性和阳性慢性髓系白血病细胞中,采用半定量RT-PCR方法检测MIP-1α、MCP-1、CCR-1、CCR-2mRNA的表达水平。结果表明MIP-1αmRNA和CCR-1mRNA在bcr/abl融合基因阳性细胞中不表达,但在bcr/abl融合基因阴性细胞中表达,而MCP-1mRNA和CCR-2mRNA在bcr/abl融合基因阳性和阴性细胞中均不表达。当P210bcr/abl融合蛋白中酪氨酸激酶被抑制后,MIP-1α和CCR-1的mRNA表达水平恢复至正常水平。结论:P210bcr/abl融合蛋白抑制慢性髓系白血病细胞中MIP-1α和CCR-1mRNA的表达,但对MCP-1和CCR-2mRNA的表达无影响。 展开更多
关键词 慢性髓系白血病 BCR/ABL融合基因 P210bcr/abl融合蛋白 mip-1Α CCR-1 MCP-1 CCR-2
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嗜肺军团菌mip基因重组质粒GFP-mip的构建及表达 被引量:1
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作者 惠英华 曹秀琴 杨志伟 《宁夏医科大学学报》 2011年第2期105-107,111,F0002,共5页
目的构建嗜肺军团菌mip基因的真核重组质粒GFP-mip,并观察其在NIH3T3细胞中的表达。方法以嗜肺军团菌DNA为模版,通过PCR扩增获得mip基因,将其定向克隆到绿色荧光质粒pEGFP-C1中,构建真核重组质粒GFP-mip。经限制性核酸内切酶XhoI和BamH... 目的构建嗜肺军团菌mip基因的真核重组质粒GFP-mip,并观察其在NIH3T3细胞中的表达。方法以嗜肺军团菌DNA为模版,通过PCR扩增获得mip基因,将其定向克隆到绿色荧光质粒pEGFP-C1中,构建真核重组质粒GFP-mip。经限制性核酸内切酶XhoI和BamHI酶切鉴定、PCR和核酸序列分析后,通过脂质体法转染到NIH3T3细胞中,利用荧光显微镜观察重组质粒的稳定表达。结果扩增出了702bpmip基因,在细胞质和细胞膜观察到较强绿色荧光。结论成功构建了真核重组质粒GFP-mip,并在NIH3T3细胞中得到了表达。 展开更多
关键词 嗜肺军团菌 mip基因 GFP-mip 蛋白表达
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趋化因子IL-8,MCP-1和MIP-1对非小细胞肺癌血管生成的作用和意义 被引量:5
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作者 邹文 胡铁辉 《中南大学学报(医学版)》 CAS CSCD 北大核心 2007年第4期665-670,共6页
目的:检测非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中趋化因子白细胞介素-8(IL-8)、单核细胞趋化蛋白-1(MCP-1)和巨噬细胞炎性蛋白-1(MIP-1)mRNA的表达,分析它们与微血管计数(MVC)的相互关系及其对NSCLC临床病理特征的意义... 目的:检测非小细胞肺癌(non-small cell lung cancer,NSCLC)组织中趋化因子白细胞介素-8(IL-8)、单核细胞趋化蛋白-1(MCP-1)和巨噬细胞炎性蛋白-1(MIP-1)mRNA的表达,分析它们与微血管计数(MVC)的相互关系及其对NSCLC临床病理特征的意义。方法:采用原位杂交法检测40例NSCLC和10例正常肺组织石蜡切片标本中IL-8,MCP-1和MIP-1mRNA的表达情况,采用免疫组织化学法测定上述标本中微血管(MV)计数。结果:40例NSCLC组织中IL-8,MCP-1和MIP-1mRNA的阳性系数均值明显高于10例肺组织对照组,差异有统计学意义,并且随着NSCLC临床病理的改变而出现相应的变化,表现为T3组>T2或T1组,III期组>II期组>I期组,有淋巴结和远处转移组>无转移组,生存时间≤3年组大于生存时间>3年组。IL-8,MCP-1和MIP-1mRNA阳性表达相互之间以及与MVC之间均存在着密切的正相关。结论:上述结果提示NSCLC组织中趋化因子IL-8,MCP-1和MIP-1可能相互协同,共同促进肿瘤血管生成,并影响肿瘤的进展、转移和预后。 展开更多
关键词 非小细胞肺癌 白介素-8 单核细胞趋化蛋白-1 巨噬细胞炎性蛋白-1 血管生成 微血管计数
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趋化因子MIP-3α的克隆与表达 被引量:1
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作者 罗福康 郑红 沈大斌 《局解手术学杂志》 2005年第2期91-93,共3页
目的 克隆人趋化因子MIP 3α基因,表达并初步纯化MIP 3α融合蛋白。方法 从扁桃体中提取总RNA ,再进行RT PCR ,扩增MIP 3α成熟蛋白基因,并在5’和3’分别添加NcoI和EcoRI酶切位点,通过这两个酶切位点重组于pET3 2a(+ )载体上,转化E .... 目的 克隆人趋化因子MIP 3α基因,表达并初步纯化MIP 3α融合蛋白。方法 从扁桃体中提取总RNA ,再进行RT PCR ,扩增MIP 3α成熟蛋白基因,并在5’和3’分别添加NcoI和EcoRI酶切位点,通过这两个酶切位点重组于pET3 2a(+ )载体上,转化E .coli.DH5α,筛选阳性克隆,酶切鉴定,DNA测序检测插入序列的正确性,缺失突变获得MIP 3α天然蛋白表达载体pET3 2a(+ ) /MIP 3α,SDS PAGE分析其表达,Westernblot验证融合蛋白。大量表达并初步纯化MIP 3α融合蛋白。结果 成功克隆了MIP 3α基因,表达并初步纯化得到MIP 3α融合蛋白。结论 构建的MIP 3α硫氧还蛋白融合表达载体以可溶性蛋白的方式表达MIP 3α硫氧还蛋白。 展开更多
关键词 mip-3Α 融合表达 载体 WESTERN BLOT 蛋白纯化
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MIP-1β对长期培养体系中造血祖细胞增殖的影响 被引量:2
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作者 吴英理 张翼军 张林生 《中国现代医学杂志》 CAS CSCD 2001年第1期21-23,共3页
目的 :探讨MIP - 1β对长期培养体系中造血祖细胞增殖的影响。方法 :在骨髓长期培养的第 3、4、5周 ,分别加入MIP - 1β ,每周半换液时换出上清进行细胞计数 ,做CFU -GM培养。第 6周做3HTdR自杀实验 ,检测CFU -HPP。结果 :加MIP - 1β... 目的 :探讨MIP - 1β对长期培养体系中造血祖细胞增殖的影响。方法 :在骨髓长期培养的第 3、4、5周 ,分别加入MIP - 1β ,每周半换液时换出上清进行细胞计数 ,做CFU -GM培养。第 6周做3HTdR自杀实验 ,检测CFU -HPP。结果 :加MIP - 1β组上清中有核细胞数 ,CFU -GM数较对照组略有增加 ,但无显著差异(P >0 .0 5 ) ;第 6周MIP - 1β组造血祖细胞3HTdR自杀率较对照组明显增高。 (P <0 .0 5 )。CFU -HPP与对照组无显著差异 (P >0 .0 5 )。结论 :MIP - 1β可解除骨髓基质层的内源性抑制活性 。 展开更多
关键词 巨噬细胞炎症蛋白1β 骨髓长期培养 造血祖细胞
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血清TTF-1、MIP-1α水平与甲状腺乳头状微小癌的关系研究 被引量:9
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作者 杨雪 孙晓菲 +4 位作者 范慧洁 崔国敏 于江红 董其娟 王慧君 《实用癌症杂志》 2018年第5期735-738,共4页
目的探讨TTF-1、MIP-1α在PTMC诊断中的临床价值,为临床PTMC的诊断提供新途径。方法选择PTC患者42例、PTMC患者45例及TD患者40例做为研究对象,所有患者均经病理确诊。所有患者经病理确诊并入组后,取空腹静脉血,采用酶联免疫法检测血清TT... 目的探讨TTF-1、MIP-1α在PTMC诊断中的临床价值,为临床PTMC的诊断提供新途径。方法选择PTC患者42例、PTMC患者45例及TD患者40例做为研究对象,所有患者均经病理确诊。所有患者经病理确诊并入组后,取空腹静脉血,采用酶联免疫法检测血清TTF-1、MIP-1α水平。比较三组患者血清TTF-1、MIP-1α结果差异。结合病理诊断结果,将三组患者的血清TTF-1、MIP-1α水平分别制作ROC曲线,确定三组患者血清TTF-1、MIP-1α的临界限值。根据血清TTF-1、MIP-1α的临界限值,采用不同的组合(血清TTF-1、MIP-1α、血清TTF-1+MIP-1α)对所有患者分别做出PTC、PTMC、TC的诊断结果,计算血清TTF-1、MIP-1α、血清TTF-1+MIP-1α诊断PTMC的灵敏度、特异度和准确度,并比较不同方案的诊断价值。结果三组患者一般资料比较差异无统计学意义(P>0.05)。PTC组患者血清TTF-1、MIP-1α水平均明显高于PTMC和TD患者(P<0.05),PTMC组患者血清TTF-1、MIP-1α水平均高于TD组患者(P<0.05)。血清TTF-1指标的ROC曲线左侧拐点为(4.3μg/L),血清MIP-1αROC曲线左侧拐点为(55.6 ng/L)。血清TTF-1+MIP-1α诊断PTMC的灵敏度、特异度均明显高于单纯的血清TTF-1、MIP-1α。结论血清TTF-1、MIP-1α与甲状腺癌变程度关系密切,血清TTF-1联合MIP-1α诊断PTMC具有较高的临床价值,避免了高频超声诊断的设备和操作人员的经验限制,诊断PTMC具有一定的临床价值。 展开更多
关键词 甲状腺乳头状微小癌 甲状腺转录因子 巨噬细胞炎性蛋白1Α 诊断价值
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红玉赔赈颗粒对脓毒症患者血清MIP-2和sTREM-1的影响及其与中医症候相关性研究 被引量:2
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作者 朱亮 赵雷 +3 位作者 沈梦雯 顾雯艳 钱义明 钱风华 《中国急救医学》 CAS CSCD 北大核心 2019年第11期1074-1079,共6页
目的探讨红玉赔赈颗粒对脓毒症患者血清巨噬细胞炎症蛋白-2(MIP-2)、血清可溶性髓样细胞触发受体-1(sTREM-1)的影响及炎症指标与中医症候量表的相关性.方法将70例符合脓毒症诊断标准的急危重病症患者随机分为两组:试验组在西医常规治疗... 目的探讨红玉赔赈颗粒对脓毒症患者血清巨噬细胞炎症蛋白-2(MIP-2)、血清可溶性髓样细胞触发受体-1(sTREM-1)的影响及炎症指标与中医症候量表的相关性.方法将70例符合脓毒症诊断标准的急危重病症患者随机分为两组:试验组在西医常规治疗的基础上,予以连续7d口服(或鼻饲)红玉赔赈颗粒;对照组在西医常规治疗的基础上加用1/10的红玉赔赈颗粒安慰剂.用酶联免疫吸附法(ELISA)检测脓毒症患者治疗前(D0)及治疗第1天(D1)、第3天(D3)、第7天(D7)血清MIP-2、sTREM-1水平,观察并记录患者生命体征及中医症候评分.结果治疗前两组MIP-2比较差异无统计学意义(P=0.66);治疗后两组MIP-2均下降,D7试验组优于对照组(pg/L:78.45±41.78 vs.111.40±72.95,P<0.05);D1、D3、D7两组与同组治疗前比较差异均有统计学意义(P<0.05).治疗前两组sTREM-1比较差异无统计学意义(P=0.895);治疗后两组sTREM-1均下降,试验组D7、对照组D3及D7 sTREM与同组治疗前比较差异有统计学意义(P<0.05),D7试验组优于对照组(pg/L:112.01±40.56 vs.150.80±53.95,P<0.05).治疗前两组中医症候评分比较差异无统计学意义(P=0.607);治疗后两组评分均下降,D1、D3试验组优于对照组(分:20.86±2.41 vs.22.25±2.26,18.57±3.37 vs.20.17±2.21,P<0.05);D3和D7两组与同组治疗前比较差异有统计学意义(P<0.05).中医证候评分与治疗前后血清MIP-2、sTREM-1水平皆呈直线相关.结论血清MIP-2、sTREM-1可以作为评价脓毒症气分证时病情程度的辅助指标;红玉赔赈颗粒可辅助降低脓毒症患者的血清MIP-2、sTREM-1水平,抑制过度的炎症反应,改善预后. 展开更多
关键词 脓毒症 红玉赔赈颗粒 巨噬细胞炎症蛋白-2(mip-2) 可溶性髓样细胞触发受体-1(sTREM-1) 中医治疗
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