|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | MSX2 mediates entry of human pluripotent stem cells into mesendoderm by simultaneously suppressing SOX2 and activating NODAL signaling显示文摘发信号的 BMP 怎么集成到并且使动摇人的 pluripotent 干细胞(hPSCs ) 的 pluripotency 电路开始区别进单个细菌层是一个长期的难题。这里,我们报导肌肉片断 homeobox 2 (MSX2 ) , msh 家庭的一个 homeobox 抄写因素, BMP 发信号的直接目标基因和 hPSC 到 mesendoderm 的区别的一个主人调停人。MSX2 的强制表示足够废除 pluripotency 并且导致 hPSCs 的指导 mesendoderm 区别,当 MSX2 弄空损害 mesendoderm 正式就职时。MSX2 是在 hPSCs 的 BMP 小径的直接目标基因,并且能被 Wnt 信号 synergistically 在 mesendoderm 正式就职期间经由 LEF1 激活。而且, MSX2 使动摇通过到 SOX2 倡导者和 SOX2 抄写的压抑的直接绑定的 pluripotency 电路,当 MSX2 通过节的倡导者的直接绑定和激活由 SOX2 的同时的抑制和节的表示的正式就职控制 mesendoderm 系承诺时。有趣地, SOX2 能支持 MSX2 蛋白质的降级,建议在在干细胞命运的控制的二个指定系的因素之间的相互的对抗。一起,我们的调查结果揭示使动摇的关键新机制在 hPSCs 的 pluripotency 和指导系承诺。 | Qingqing Wu Leisheng Zhang Pei Su Xiaohua Lei Xin Liu Hongtao Wang Lisha Lu Yang Bai Tao Xiong Dong Li Zhengmao Zhu Enkui Duan Erlie Jiang Sizhou Feng Mingzhe Hang Yuanfu Xu Fei Wang Jiaxi Zhou | 2015 | Cell Research2015，25，12： | 8 |
| 2 | Bispecific antibody and its clinical applications in cancer显示文摘Bispecific antibody (BsAb) usually consists of two different antigen-binding arms, by which it is capable of simultaneously binding to target cells and effector cells, and can directly mediate the killing of target cells by retargeting and activating effector cells. The development of BsAb research goes through three main stages: chemical cross-linking of murine-derived monoclonal antibody, hybrid hy-bridomas and engineered BsAb. Among them, engineered BsAb has more formats than the other two, such as diabody, ScdHLX, ScZip, ScCH3, ScFab and BsIgG, etc. Compared with former murine-derived BsAbs, engineered BsAb has lower immunogenicity and stronger penetrating capacity, and currently, some of them appear suitable for clinical application in yields and qualities. Up to now, several phase I and phase II clinical studies of BsAb, for instance, some (Fab’)2 and Diabodies, have been performed. Among those BsAbs, anti-CD3/anti-tumor BsAbs is most common, they not only can activate T cell and induce CD3AK | Yuanfu Xu Chunzheng Yang Zhenping Zhu | 2001 | Chinese Science Bulletin2001，46，5： | 6 |
| 3 | A Multisource Contour Matching Method Considering the Similarity of Geometric Features显示文摘The existing multi-source contour matching studies have focused on the matching methods with consideration of topological relations and similarity measurement based on spatial Euclidean distance,while it is lack of taking the contour geometric features into account,which may lead to mismatching in map boundaries and areas with intensive contours or extreme terrain changes.In light of this,it is put forward that a matching strategy from coarse to precious based on the contour geometric features.The proposed matching strategy can be described as follows.Firstly,the point sequence is converted to feature sequence according to a feature descriptive function based on curvature and angle of normal vector.Then the level of similarity among multi-source contours is calculated by using the longest common subsequence solution.Accordingly,the identical contours could be matched based on the above calculated results.In the experiment for the proposed method,the reliability and efficiency of the matching method are verified using simulative datasets and real datasets respectively.It has been proved that the proposed contour matching strategy has a high matching precision and good applicability. | Wenyue GUO Anzhu YU Qun SUN Shaomei LI Qing XU Bowei WEN Yuanfu LI | 2020 | Journal of Geodesy and Geoinformation Science2020，3，3： | 5 |
| 4 | The role of bone marrow-derived cells in the origin of liver cancer revealed by single-cell sequencing显示文摘Objective:Epithelial cancers often originate from progenitor cells,while the origin of hepatocellular carcinoma(HCC)is still controversial.HCC,one of the deadliest cancers,is closely linked with liver injuries and chronic inflammation,which trigger massive infiltration of bone marrow-derived cells(BMDCs)during liver repair.Methods:To address the possible roles of BMDCs in HCC origination,we established a diethylnitrosamine(DEN)-induced HCC model in bone marrow transplanted mice.Immunohistochemistry and frozen tissue immunofluorescence were used to verify DENinduced HCC in the pathology of the disease.The cellular origin of DEN-induced HCC was further studied by single cell sequencing,single-cell nested PCR,and immunofluorescence-fluorescence in situ hybridization.Results:Studies by using single cell sequencing and biochemical analysis revealed that HCC cells in these mice were coming from donor mice BMDCs,and not from recipient mice.Furthermore,the copy numbers of mouse orthologs of several HCC-related genes previously reported in human HCC were also altered in our mouse model.DEN-induced HCCs exhibited a similar histological phenotype and genomic profile as human HCCs.Conclusions:These results suggested that BMDCs are an important origin of HCC,which provide important clues to HCC prevention,detection,and treatments. | Lu Chen Xianfu Yi Piao Guo Hua Guo Ziye Chen Chunyu Hou Lisha Qi Yongrong Wang Chengwen Li Peng Liu Yucun Liu Yuanfu Xu Ning Zhang | 2020 | Cancer Biology & Medicine2020，17，1： | 4 |
| 5 | Establishment of a highly efficient hematopoietic differentiation model from human embryonic stem cells for functional screening显示文摘Human embryonic stem cells(hESCs)have been successfully differentiated into hematopoietic progenitor cells with colony formation capacity and further into various kinds of blood cells including erythrocytes,megakaryocytes,neutrophils,nature killer cells and T lymphocytes[1 7].Nevertheless,the differentiation efficiency is extremely low. | PANG SuLei WU QingQing TIAN Sha SU Pei BAI Yang GAO Jie YANG YiQing LIU Xin ZHU ZhengMao XU YuanFu ZHOU JiaXi | 2013 | Science China(Life Sciences)2013，56，12： | 3 |
| 6 | Discovery of lacustrine shale deposits in the Yanshan Orogenic Belt,China: Implications for hydrocarbon exploration显示文摘The mechanism of formation of lacustrine deposits within stable orogenic belts and their potential for shale oil and gas exploration are frontier themes of challenge in the fields of sedimentology and petroleum exploration. Orogenic belts witness strong tectonic activities and normally cannot host stable lacustrine basins and deep shale formations. Therefore, basins in orogenic belts are considered to have no potential to form shale hydrocarbon reservoirs. Here we investigate the Luanping Basin located in the Yanshan orogenic belt where previous studies regarded rivers and fan deltas as the major main Mesozoic deposits. Based on detailed field exploration and scientific drilling, we report the finding of a large number of lacustrine shale continental deep-water deposits in the Mesozoic strata. Our finding of the occurrence of active shale oil and gas also in this basin also subvert the previous perceptions.We report SHRIMP zircon U-Pb age that define the bottom boundary of the target interval as 127.6 ± 1.7 Ma belonging to the early Cretaceous strata. Tectonics and climate are considered to be the main factors that controlled the deep-water sedimentation during this period. The drill cores revealed evidence of shale gas and the TOC of shale is 0.33%–3.60%, with an average value of 1.39% and Ro is 0.84%–1.21%, with an average value of 1.002%. The brittleness index of shale is between 52.7% and 100%. After vertical well fracturing, the daily gas production is more than 1000 m^(3). Our findings show that the basin has considerable potential for shale oil and gas. The geological resources of the shale gas in the Xiguayuan Fm. are estimated as 1110.12 × 10^(8) m^(3), with shale oil geological resources of 3340.152 × 10^(4) t. Our findings indicate that the Yanshan orogenic belt has potential exploration prospect. This work not only redefines the Luanping Basin as a rift deep-water Mesozoic Lake Basin, but also rules out the previous notion that the basin is dominated by shallow water sediments. The discovery of shale oil and gas also provides an important reference for subsequent petroleum exploration and development in this basin. Our study shows that shale oil and gas reservoirs can be found in the lacustrine basins of orogenic belts which were strongly influenced by volcanism. These results have significant implications for the sedimentology and oil exploration in the Qinling and Xingmeng Orogenic Belts of China, as well as those in other terranes of the world including the New England Orogenic Belt in Australia. | Yuanfu Zhang Xiaodong Yuan Min Wang Pengcheng Ge Yancui Huo Jie Xu Jianguo Zhang Jian Cheng Zaixing Jiang | 2021 | Geoscience Frontiers2021，12，6： | 2 |
| 7 | Intraoperative Detection of Thyroid Carcinoma by Fourier Transform Infrared Spectrometry显示文摘 | Xiaoqing Zhang Yizhuang Xu Yuanfu Zhang Lixin Wang Chunsheng Hou Xiaosi Zhou Xiaofeng Ling Zhi Xu | 2011 | Journal of Surgical Research2011，，2： | 1 |
| 8 | In situ growth of positively-charged gold nanoparticles on single-walled carbon nanotubes as a highly active peroxidase mimetic and its application in biosensing显示文摘 | Zhang Yuanfu Xu Chunli Li Baoxin | 2013 | Biosens Bioelectron2013，43，1： | 1 |
| 9 | Efficacy of anti-CD20 chimeric Fab' fragment on proliferation of B lymphoma cells显示文摘The variable domain of heavy chain (VH) and light chain (VL) genes of anti-CD20 monoclonal antibody HL47 were cloned from anti-CD20 ScFv expression vector pCANBTEcd20 by PCR and ligated into vector pYZF to construct chimeric anti-CD20 Fab’ fragment expression vector pTZFcd20. Chimeric anti-CD20 Fab’ fragment was expressed in E. coli 16C9 and purified by protein G affinity chromatography. Competitive inhibition assay showed that anti-CD20 Fab’ fragment inhibited binding of HI47 to CD20 on the surface of Daudi cells. Results from MTT assay indicated that chimeric anti-CD20 Fab’fragment inhibited the proliferation of Daudi cells, IC50=69 ug/mL. Affinity of chimeric anti-CD20 Fab’ fragment was determined, Ka was about 8.9×108 (mol/L)-1. | LAI Zengzu XIONG Dongsheng FAN Dongmei XU Yuanfu LIU Hanzhi PENG Hui ZHU Zhenping YANG Chunzheng | 2001 | Chinese Science Bulletin2001，46，14： | 1 |
| 10 | Perivascular localized cells commit erythropoiesis in PDGF-B-expressing solid tumors显示文摘Background:Tumors possess incessant growth features,and expansion of their masses demands sufficient oxygen supply by red blood cells(RBCs).In adult mammals,the bone marrow(BM)is the main organ regulating hematopoiesis with dedicated manners.Other than BM,extramedullary hematopoiesis is discovered in various pathophysiological settings.However,whether tumors can contribute to hematopoiesis is completely unknown.Accumulating evidence shows that,in the tumor microenvironment(TME),perivascular localized cells retain progenitor cell properties and can differentiate into other cells.Here,we sought to better understand whether and how perivascular localized pericytes in tumors manipulate hematopoiesis.Methods:To test if vascular cells can differentiate into RBCs,genome-wide expression profiling was performed using mouse-derived pericytes.Genetic tracing of perivascular localized cells employing NG2-CreERT2:R26R-tdTomato mouse strain was used to validate the findings in vivo.Fluorescence-activated cell sorting(FACS),single-cell sequencing,and colony formation assays were applied for biological studies.The production of erythroid differentiationspecific cytokine,erythropoietin(EPO),in TME was checked using quantitative polymerase chain reaction(qPCR),enzyme-linked immunosorbent assay(ELISA,magnetic-activated cell sorting and immunohistochemistry.To investigate BM function in tumor erythropoiesis,BM transplantation mouse models were employed.Results:Genome-wide expression profiling showed that in response to plateletderived growth factor subunit B(PDGF-B),neural/glial antigen 2(NG2)+perivascular localized cells exhibited hematopoietic stem and progenitor-like features and underwent differentiation towards the erythroid lineage.PDGF-B simultaneously targeted cancer-associated fibroblasts to produce high levels of EPO,a crucial hormone that necessitates erythropoiesis.FACS analysis using genetic tracing of NG2+cells in tumors defined the perivascular localized cell-derived subpopulation of hematopoietic cells.Single-cell sequencing and colony formation assays validated the fact that,upon PDGF-B stimulation,NG2+cells isolated from tumors acted as erythroblast progenitor cells,which were distinctive from the canonical BM hematopoietic stem cells.Conclusions:Our data provide a new concept of hematopoiesis within tumor tissues and novel mechanistic insights into perivascular localized cell-derived erythroid cells within TME.Targeting tumor hematopoiesis is a novel therapeutic concept for treating various cancers that may have profound impacts on cancer therapy. | Kayoko Hosaka Chenchen Wang Shiyue Zhang Xue Lv Takahiro Seki Yin Zhang Xu Jing Jieyu Wu Qiqiao Du Xingkang He Yulong Fan Xuan Li Makoto Kondo Masahito Yoshihara Hong Qian Lihong Shi Ping Zhu Yuanfu Xu Yunlong Yang Tao Cheng Yihai Cao | 2023 | Cancer Communications2023，43，6： | 1 |
| 11 | TNFα inhibitor C87 sensitizes EGFRvⅢ transfected glioblastoma cells to gefitinib by a concurrent blockade of TNFα signaling显示文摘Objective: More than half of human glioblastomas show EGFR gene amplification and mutation, but EGFR inhibitors have not been effective in treating EGFR-positive glioblastoma patients.The mechanism behind this type of primary resistance is not well understood.The aim of this study was to investigate gefitinib resistance in glioblastoma, and explore ways to circumvent this significant clinical problem.Methods: MTT method was used to test the cell viability after EGFR-positive glioblastoma cells were treated with indicated drugs;real-time quantitative PCR method was included to detect the TNFα mRNA levels in glioma tissues and cell lines.ELISA was introduced to measure the TNFα protein levels in cell culture supernatant of glioblastoma cells treated with gefitinib.Western blot was used to detect the activity change of intracellular kinases in drug-treated glioblastoma cells.Two mouse xenograft tumor models were carried out to evaluate the in vivo effects of a combination of EGFR and TNFα inhibitors.Results: We found that glioblastoma resistance to gefitinib may be mediated by an adaptive pro-survival TNFα-JNK-Axl signaling axis, and that high TNFα levels in the glioblastoma microenvironment may further intensify primary resistance.A combination of the TNFα-specific small-molecule inhibitor C87 and gefitinib significantly enhanced the sensitivity of glioblastoma cells to gefitinib in vitro and in vivo.Conclusions: Our findings provide a possible explanation for the primary resistance of glioblastoma to EGFR inhibitors and suggest that dual blockade of TNFα and EGFR may be a viable therapeutic strategy for the treatment of patients with chemotherapy-refractory advanced glioblastoma. | Li Ma Chunhua She Qian Shi Qiang Yin Xinxin Ji Yongrong Wang Yulong Fan Xinyao Kong Peng Li Zengfeng Sun Xiaohui Zhang Zhen Zhang Jian Wang Tong Wang Yuanfu Xu Wenliang Li | 2019 | Cancer Biology & Medicine2019，16，3： | 1 |
| 12 | Aφ6-m Tunnel Boring Machine Steel Arch Splicing Manipulator显示文摘Robotic splicing of steel arches is a challenging task that is necessary to realize the grasping and docking of steel arches in a limited space.Steel arches often have a mass of more than 200 kg and length of more than 4 m.Owing to the large volume and mass of steel arches and the high requirements for accurately positioning the splicing,it is difficult for a general manipulator to meet the stiffness requirements.To enhance the structural stiffness of the steel arch splicing manipulator,a single-degree-of-freedom(DOF)closed-loop mechanism was added to the grasping structure of the manipulator.Based on the basic principle of structural synthesis,a solution model of the single-DOF closed-loop mechanism was developed,and alternative kinematic pairs of the mechanism with different input constraints and output requirements were derived.Based on this model,a design method for a single-DOF closed-loop grasping mechanism and a posture adjustment mechanism for a steel arch was devised.Combined with the same dimensional subspace equivalence principle of the graphical-type synthesis method,12 types of steel arch splicing manipulator were constructed.By analyzing the motion/force transmission and structural complexity of the steel arch splicing manipulators,the best scheme was selected.A prototype of the steel arch splicing manipulator was manufactured.Adams software was used to obtain clearly the output trajectory of the end of the manipulator.The relative spatial positions of the upper and lower jaws under different working stages were analyzed,demonstrating that the manipulator satisfied the grasping requirements.Through a steel arch splicing experiment,the grasping effect,docking accuracy,and splicing efficiency of the manipulator met the design requirements.The steel arch splicing manipulator can replace the manual completion of the steel arch splicing operation,significantly improving the operation efficiency. | Yuanfu He Yimin Xia Zhen Xu Jie Yao Bo Ning Xuemeng Xiao | 2022 | Chinese Journal of Mechanical Engineering2022，35，2： | 0 |
| 13 | Noninvasive Surface Detection of Papillary Thyroid Carcinoma by Fourier Transform Infrared Spectroscopy显示文摘 | ZHANG Weitao TIAN Peirong ZHU Qing ZHANG Yuanfu CUI Long XU Zhi | 2015 | Chemical Research in Chinese Universities2015，31，2： | 0 |
| 14 | Supramolecular nano drug delivery systems mediated via host-guest chemistry of cucurbit[n]uril(n=6 and 7)显示文摘As a novel family of macrocyclic molecules,cucurbit[n]urils(CB[n]s) have emerged as promising building blocks of supramolecular nano drug delivery systems(SNDDS) in recent years.Direct encapsulation of amphiphilic guests by CB[6] and CB[7] can modulate their amphiphilicity,resulting in formation of supramolecular amphiphiles that self-assemble into supramolecular nanoparticles for drug delivery.Additionally,CB[n]'s host-guest chemistry on the surface of mesoporous nanoparticles makes CB[n] an ideal blocking agent to control drug release from delivery vehicles.These SNDDS possess intrinsic stimuli responsiveness towards external guest or host,which can further incorporate re s ponsiveness to a variety of other stimuli including pH,thermal,redox,photo and enzyme,to realize multiple stimuli-responsive drug release.Moreover,the recent breakthrough in direct functionalization of CB[n]s has provided a feasible method for preparing superior CB[6] and CB[7] derivatives that can be employed to build multifunctional SNDDS with unoccupied macrocycles located on surface,which could be decorated with various functional 'tags' through host-guest chemistry.In this review,we summarized the recent progress of CB[6] and CB[7] based SNDDS through formation of supramolecular amphiphiles,supramolecular nanovalves as well as supramolecularly tailorable surface,which we hope to further promote the development of CB[n]s family as building blocks for advanced SNDDS. | Shengke Li Yan Gao Yuanfu Ding Anni Xu Huaping Tan | 2021 | Chinese Chemical Letters2021，32，1： | 0 |
| 15 | Supramolecular Vesicles Based on Gold Nanorods for Precise Control of Gene Therapy and Deferred Photothermal Therapy显示文摘In spite of being a promising therapeutic modality,gene therapy has limited clinical applications,mostly due to the lack of spatiotemporal resolution and inadequate efficacy.Herein,we present a facile strategy to remotely control intracellular gene expression by using gold nanorod-(Au NR)derived,host-guest interaction-mediated supramolecular vesicles as a gene carrier and photothermal transducer.Upon pulsed laser irradiation,mild photothermal conditions dissociate supramolecular vesicles to release gene and simultaneously activate heat shock protein-70 promoter(Hsp70)for spatiotemporally initiating gene expression inside cancer cells.Subsequently,upon introducing a polymeric guest species specifically into cancer cells,the dissociated Au NRs functionalized with macrocyclic host molecules could re-aggregate rapidly in cells to retard exocytosis of these NRs,thereby allowing deferred photothermal therapy to enhance the overall therapeutic outcome. | Ludan Yue Kuikun Yang Jianwen Wei Mengze Xu Chen Sun Yuanfu Ding Zhen Yuan Shu Wang Ruibing Wang | 2022 | CCS Chemistry2022，4，5： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员