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  1. Article ; Online: Evaluation of the TLR3 involvement during Schistosoma japonicum-induced pathology.

    Xie, Hongyan / Chen, Dianhui / Feng, Yuanfa / Mo, Feng / Liu, Lin / Xing, Junmin / Xiao, Wei / Gong, Yumei / Tang, Shanni / Tan, Zhengrong / Liang, Guikuan / Zhao, Shan / Yin, Weiguo / Huang, Jun

    BMC immunology

    2024  Volume 25, Issue 1, Page(s) 2

    Abstract: Background: Despite the functions of TLRs in the parasitic infections have been extensively reported, few studies have addressed the role of TLR3 in the immune response to Schistosoma japonicum infections. The aim of this study was to investigate the ... ...

    Abstract Background: Despite the functions of TLRs in the parasitic infections have been extensively reported, few studies have addressed the role of TLR3 in the immune response to Schistosoma japonicum infections. The aim of this study was to investigate the properties of TLR3 in the liver of C57BL/6 mice infected by S. japonicum.
    Methods: The production of TLR3
    Results: Flow cytometry results showed that the expression of TLR3 increased significantly after S. japonicum infection (P < 0.05). Hepatic myeloid and lymphoid cells could express TLR3, and the percentages of TLR3-expressing MDSC, macrophages and neutrophils were increased after infection. Knocking out TLR3 ameliorated the damage and decreased infiltration of inflammatory cells in infected C57BL/6 mouse livers.,The number of WBC was significantly reduced in TLR3 KO-infected mice compared to WT-infected mice (P < 0.01), but the levels of RBC, platelet and HGB were significantly increased in KO infected mice. Moreover, the relative titers of anti-SEA IgG and anti-SEA IgM in the serum of infected KO mice were statistically decreased compared with the infected WT mice. We also compared the activation-associated molecules expression between S.japonicum-infected WT and TLR3 KO mice.
    Conclusions: Taken together, our data indicated that TLR3 played potential roles in the context of S. japonicum infection and it may accelerate the progression of S. japonicum-associated liver pathology.
    MeSH term(s) Animals ; Mice ; Schistosoma japonicum/metabolism ; Toll-Like Receptor 3/metabolism ; Mice, Inbred C57BL ; Immunoglobulin G ; Immunoglobulin M
    Chemical Substances Toll-Like Receptor 3 ; Immunoglobulin G ; Immunoglobulin M ; TLR3 protein, mouse
    Language English
    Publishing date 2024-01-03
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2041500-X
    ISSN 1471-2172 ; 1471-2172
    ISSN (online) 1471-2172
    ISSN 1471-2172
    DOI 10.1186/s12865-023-00586-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Characteristics of splenic PD-1

    Chen, Dianhui / Mo, Feng / Liu, Meiling / Liu, Lin / Xing, Junmin / Xiao, Wei / Gong, Yumei / Tang, Shanni / Tan, Zhengrong / Liang, Guikuan / Xie, Hongyan / Huang, Jun / Shen, Juan / Pan, Xingfei

    Immunologic research

    2024  

    Abstract: Although the functions of programmed death-1 (PD-1) on αβ T cells have been extensively reported, a role for PD-1 in regulating γδT cell function is only beginning to emerge. Here, we investigated the phenotypic and functional characteristics of PD-1- ... ...

    Abstract Although the functions of programmed death-1 (PD-1) on αβ T cells have been extensively reported, a role for PD-1 in regulating γδT cell function is only beginning to emerge. Here, we investigated the phenotypic and functional characteristics of PD-1-expressing γδT cells, and the molecular mechanism was also explored in the Plasmodium yoelii nigeriensis (P. yoelii NSM)-infected mice. Flow cytometry and single-cell RNA sequencing (scRNA-seq) were performed. An inverse agonist of RORα, SR3335, was used to investigate the role of RORα in regulating PD-1
    Language English
    Publishing date 2024-01-24
    Publishing country United States
    Document type Journal Article
    ZDB-ID 632857-x
    ISSN 1559-0755 ; 0257-277X
    ISSN (online) 1559-0755
    ISSN 0257-277X
    DOI 10.1007/s12026-023-09441-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Correction to: Characteristics of splenic PD-1

    Chen, Dianhui / Mo, Feng / Liu, Meiling / Liu, Lin / Xing, Junmin / Xiao, Wei / Gong, Yumei / Tang, Shanni / Tan, Zhengrong / Liang, Guikuan / Xie, Hongyan / Huang, Jun / Shen, Juan / Pan, Xingfei

    Immunologic research

    2024  

    Language English
    Publishing date 2024-02-29
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 632857-x
    ISSN 1559-0755 ; 0257-277X
    ISSN (online) 1559-0755
    ISSN 0257-277X
    DOI 10.1007/s12026-024-09469-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Immunological characteristics of CD103

    Shi, Feihu / Tang, Shanni / Chen, Dianhui / Mo, Feng / Li, Jiajie / Fang, Chao / Wei, Haixia / Xing, Junmin / Liu, Lin / Gong, Yumei / Tan, Zhengrong / Zhang, Ziqi / Pan, Xingfei / Zhao, Shan / Huang, Jun

    Parasitology research

    2023  Volume 122, Issue 11, Page(s) 2513–2524

    Abstract: CD103 is an important marker of tissue-resident memory T cells (TRM) which play important roles in fighting against infection. However, the immunological characteristics of ... ...

    Abstract CD103 is an important marker of tissue-resident memory T cells (TRM) which play important roles in fighting against infection. However, the immunological characteristics of CD103
    MeSH term(s) Animals ; Mice ; CD8-Positive T-Lymphocytes/metabolism ; Interleukin-10/metabolism ; Interleukin-17 ; Interleukin-4 ; Liver ; Malaria/immunology ; Malaria/metabolism ; Mice, Inbred C57BL ; Plasmodium yoelii
    Chemical Substances Interleukin-10 (130068-27-8) ; Interleukin-17 ; Interleukin-4 (207137-56-2) ; alpha E integrins
    Language English
    Publishing date 2023-09-14
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 284966-5
    ISSN 1432-1955 ; 0932-0113 ; 0044-3255
    ISSN (online) 1432-1955
    ISSN 0932-0113 ; 0044-3255
    DOI 10.1007/s00436-023-07950-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: TLR7 enhancing follicular helper T (Tfh) cells response in C57BL/6 mice infected with Plasmodium yoelii NSM TLR7 mediated Tfh cells in P. yoelii infected mice.

    Yang, Quan / Zhou, Lu / Tan, Zhengrong / Zhu, Yiqiang / Mo, Lengshan / Fang, Chao / Li, Jiajie / Chen, Chen / Luo, Ying / Wei, Haixia / Yin, Weiguo / Huang, Jun

    Immunology

    2023  Volume 171, Issue 3, Page(s) 413–427

    Abstract: Toll-like receptors (TLRs) play an important role in inducing innate and acquired immune responses against infection. However, the effect of Toll-like receptor 7 (TLR7) on follicular helper T (Tfh) cells in mice infected with Plasmodium is still not ... ...

    Abstract Toll-like receptors (TLRs) play an important role in inducing innate and acquired immune responses against infection. However, the effect of Toll-like receptor 7 (TLR7) on follicular helper T (Tfh) cells in mice infected with Plasmodium is still not clear. The results showed that the splenic CD4
    MeSH term(s) Animals ; Mice ; Malaria ; Mice, Inbred C57BL ; Mice, Knockout ; Parasitemia/metabolism ; Plasmodium yoelii/metabolism ; T Follicular Helper Cells/metabolism ; T-Lymphocytes, Helper-Inducer ; Toll-Like Receptor 7/metabolism
    Chemical Substances Toll-Like Receptor 7 ; Tlr7 protein, mouse
    Language English
    Publishing date 2023-12-27
    Publishing country England
    Document type Journal Article
    ZDB-ID 80124-0
    ISSN 1365-2567 ; 0019-2805 ; 0953-4954
    ISSN (online) 1365-2567
    ISSN 0019-2805 ; 0953-4954
    DOI 10.1111/imm.13736
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: TLR7 modulates extramedullary splenic erythropoiesis in P. yoelii NSM-infected mice through the regulation of iron metabolism of macrophages with IFN-γ.

    Li, Jiajie / Liu, Lin / Xing, Junmin / Chen, Dianhui / Fang, Chao / Mo, Feng / Gong, Yumei / Tan, Zhengrong / Liang, Guikuan / Xiao, Wei / Tang, Shanni / Wei, Haixia / Zhao, Shan / Xie, Hongyan / Pan, Xingfei / Yin, Xiaomao / Huang, Jun

    Frontiers in immunology

    2023  Volume 14, Page(s) 1123074

    Abstract: Splenomegaly is a prominent clinical manifestation of malaria and the causes remain incompletely clear. Anemia is induced in malaria and extramedullary splenic erythropoiesis is compensation for the loss of erythrocytes. However, the regulation of ... ...

    Abstract Splenomegaly is a prominent clinical manifestation of malaria and the causes remain incompletely clear. Anemia is induced in malaria and extramedullary splenic erythropoiesis is compensation for the loss of erythrocytes. However, the regulation of extramedullary splenic erythropoiesis in malaria is unknown. An inflammatory response could facilitate extramedullary splenic erythropoiesis in the settings of infection and inflammation. Here, when mice were infected with rodent parasites,
    MeSH term(s) Mice ; Animals ; Spleen/metabolism ; Erythropoiesis ; Toll-Like Receptor 7 ; Mice, Inbred C57BL ; Interferon-gamma/therapeutic use ; Malaria ; Macrophages/metabolism ; Iron/metabolism
    Chemical Substances Toll-Like Receptor 7 ; Interferon-gamma (82115-62-6) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2023-04-27
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1123074
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Integrin Targeted MR Imaging

    Mingqian Tan, Zheng-Rong Lu

    Theranostics, Vol 1, Iss 1, Pp 83-

    2011  Volume 101

    Abstract: Magnetic resonance imaging (MRI) is a powerful medical diagnostic imaging modality for integrin targeted imaging, which uses the magnetic resonance of tissue water protons to display tissue anatomic structures with high spatial resolution. Contrast ... ...

    Abstract Magnetic resonance imaging (MRI) is a powerful medical diagnostic imaging modality for integrin targeted imaging, which uses the magnetic resonance of tissue water protons to display tissue anatomic structures with high spatial resolution. Contrast agents are often used in MRI to highlight specific regions of the body and make them easier to visualize. There are four main classes of MRI contrast agents based on their different contrast mechanisms, including T 1 , T 2 , chemical exchange saturation transfer (CEST) agents, and heteronuclear contrast agents. Integrins are an important family of heterodimeric transmembrane glycoproteins that function as mediators of cell-cell and cell-extracellular matrix interactions. The overexpressed integrins can be used as the molecular targets for designing suitable integrin targeted contrast agents for MR molecular imaging. Integrin targeted contrast agent includes a targeting agent specific to a target integrin, a paramagnetic agent and a linker connecting the targeting agent with the paramagnetic agent. Proper selection of targeting agents is critical for targeted MRI contrast agents to effectively bind to integrins for in vivo imaging. An ideal integrin targeted MR contrast agent should be non-toxic, provide strong contrast enhancement at the target sites and can be completely excreted from the body after MR imaging. An overview of integrin targeted MR contrast agents based on small molecular and macromolecular Gd(III) complexes, lipid nanoparticles and superparamagnetic nanoparticles is provided for MR molecular imaging. By using proper delivery systems for loading sufficient Gd(III) chelates or superparamagnetic nanoparticles, effective molecular imaging of integrins with MRI has been demonstrated in animal models.
    Keywords Medicine ; R
    Subject code 500
    Language English
    Publishing date 2011-01-01T00:00:00Z
    Publisher Ivyspring International Publisher
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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