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  • Open Access

    ARTICLE

    M1 macrophage-derived exosomes moderate the differentiation of bone marrow mesenchymal stem cells

    TAILIN WU1,#, XIANG ZHOU2,#, CANHUA YE1, WENCAN LU1, HAITAO LIN1, YANZHE WEI1, ZEKAI KE1, ZHENGJI HUANG1, JIANZHOU LUO1, HUIREN TAO1, CHUNGUANG DUAN1,*

    BIOCELL, Vol.46, No.2, pp. 495-503, 2022, DOI:10.32604/biocell.2022.015214 - 20 October 2021

    Abstract Differentiated macrophages have been proven to participate in the development of mesenchymal stem cells in different tissues. However, the regulatory processes remain obscure. Exosomes, which are key secretions of macrophages, have attracted increasing attention. Therefore, macrophage-derived exosomes may modulate the development of Bone marrow mesenchymal stem cells (BMMSCs). Different culture conditions were used to induce M1 polarization in THP1 cells. Subsequently, exosomes derived from unpolarized (M0) and polarized (M1) macrophages were isolated, BMMSCs were cultured with normal complete medium or inductive medium supplemented with M0 or M1 derived exosomes, and the osteogenic capacity of the… More >

  • Open Access

    ARTICLE

    GP30 of the mycobacteriophage CASbig impairs mycobacterial adaptation during acidic stress and in macrophages

    WU LI1, JIANGZHE SI2, SHUAI QIU2, JING LUO1, HUIQIONG SUN1, XIAOQING LI1, ZHIBIN WAN1, WEI GAO1, HANLU ZOU1, LEI ZHANG2, XIAOHONG XIANG3, YANZHANG LI2, TIESHAN TENG2,*

    BIOCELL, Vol.44, No.4, pp. 695-701, 2020, DOI:10.32604/biocell.2020.011941 - 24 December 2020

    Abstract The rapid emergence of multidrug-resistant and extensively drug-resistant Tuberculosis retrieved intense interest in phage-based therapy. This old approach, which was abandoned in the west in the 1940s but is generating renewed interest, has stimulated fresh research on mycobacteriophages and their lytic efficiency against their hosts. GP30 is a novel protein of the mycobacteriophage CASbig with undiscovered function. In this study, we analyzed the role of CASbig gp30 in the host Mycobacterium smegmatis. Overexpression of gp30 in the host led to reduced growth in acidic medium and attenuated the intracellular survival rate of M. smegmatis inside the THP-1 More >

  • Open Access

    ARTICLE

    Age-related modifications of macrophages influenced by “inflammageing” in graft vs. host disease

    YAQUN HONG1,2, BO WAN3, XIAOFAN LI1,4,*

    BIOCELL, Vol.44, No.2, pp. 237-246, 2020, DOI:10.32604/biocell.2020.08887 - 27 May 2020

    Abstract Most studies focus on the adaptive immune cells in the GVHD pathogenesis, while little is known about innate immune cells in GVHD occurrence and development, especially macrophages. Meanwhile, a higher incidence of graft versus host disease (GVHD) is also found in the elderly patients. Though advances have been made in the modification of macrophages influenced by the inflamm-ageing, there is still no review on the role of macrophages in GVHD and the association between GVHD and the altered macrophages by inflamm-ageing. In this review, we focus on the potential age-related modifications of macrophage in GVHD, More >

  • Open Access

    ARTICLE

    Association of TRIM22 with the type 1 interferon response during primary human cytomegalovirus infection in THP-1 macrophages

    Wei LI, Huihui GAO, Ran TAO, Lifang LIU, Shiqiang SHANG*

    BIOCELL, Vol.43, No.4, pp. 285-291, 2019, DOI:10.32604/biocell.2019.08177

    Abstract As a response factor of interferon, tripartite motif (TRIM) 22 was reported to exert antiviral activity against viruses. In this study, THP-1 macrophages were infected with human cytomegalovirus (HCMV) to establish the HCMV lytic infection model. The mRNA levels of interleukin-6 (IL-6), tumor necrosis factor-alpha (TNF-α) and interferonbeta (IFN-β) were significantly up-regulated in THP-1 macrophages at different infection time and titers. Moreover, for the first time, upregulation of TRIM22 expression was found during HCMV infection at both mRNA and protein levels in THP-1 macrophages. Furthermore, IFN-β could induce TRIM22 expression in THP-1 macrophages or HCMV More >

  • Open Access

    ABSTRACT

    Macrophages as A Mechano-Transducer to Direct the Osteogenic Differentiation of Mesenchymal Stem Cells

    Lili Dong1, Yang Song1,*, Li Yang1,*

    Molecular & Cellular Biomechanics, Vol.16, Suppl.2, pp. 78-78, 2019, DOI:10.32604/mcb.2019.07130

    Abstract It has been widely recognized that stem cells possess the potential of osteogenic differentiation, which greatly contribute to bone repair. Recently, accumulating evidences have indicated that mechanical cues are required for bone repair [1,2]. However, how local and recruited stem cells in the bone architecture receive the mechanical signals is poorly understood [3,4]. The purpose of this study is to demonstrate that macrophages potentially transduce the mechanical signals for stem cell osteogenic lineage. This demonstration has been carried out through a co-culture system to investigate the effect of macrophages which subjected to cyclic stretch on the… More >

  • Open Access

    REVIEW

    The Peritoneal Macrophages in Inflammatory Diseases and Abdominal Cancers

    Ting Liu1, Fang Liu1, Lei-Wen Peng, Li Chang, Yong-Mei Jiang

    Oncology Research, Vol.26, No.5, pp. 817-826, 2018, DOI:10.3727/096504017X15130753659625

    Abstract Peritoneal macrophages (PMs) are the major cell type of peritoneal cells that participate in multiple aspects of innate and acquired immunity in the peritoneal cavity. PMs have an ability to release a large amount of proinflammatory and anti-inflammatory cytokines and therefore play a critical role in regulating the differentiation of innate immune cells and inflammatory T cells. Accumulating studies demonstrate that the immunological reactions and inflammatory responses of PMs are strongly related to the pathogenic processes of various inflammatory diseases and abdominal cancers. Consequently, the regulation of PM activation has gradually emerged as a promising More >

  • Open Access

    ARTICLE

    Buprenorphine differentially affects M1- and M2-polarized macrophages from human umbilical cord blood

    Juan Suna, Wei Guoa, Xingguang Du

    European Cytokine Network, Vol.28, No.2, pp. 85-92, 2017, DOI:10.1684/ecn.2017.0392

    Abstract Background: As a partial μ-opioid receptor agonist with long half-life time, buprenorphine has been widely used to relieve chronic cancer and nonmalignant pain. The maintenance of chronic pain involves inflammation; however whether buprenorphine has anti-inflammation property remains unclear. Methods: Macrophages, the immune cells that initiate and maintain inflammation, were isolated from human umbilical cord blood, and were polarized into M1 or M2 macrophages with IFN-γ in the presence of lipopolysaccharide (LPS) or IL-4, respectively. Quantitative PCR, ELISA, Western blotting analysis, and chromatin immunoprecipitation assays were employed to characterize M1 and M2 macrophages. Results: 1) Buprenorphine… More >

  • Open Access

    ARTICLE

    PRR signaling during in vitro macrophage differentiation from progenitors modulates their subsequent response to inflammatory stimuli

    Alba Martínez1,2, Cristina Bono1,2, Javier Megías3, Alberto Yánez˜4,5, Daniel Gozalbo1,2, M. Luisa Gil1,2

    European Cytokine Network, Vol.28, No.3, pp. 102-110, 2017, DOI:10.1684/ecn.2017.0398

    Abstract Toll-like receptor (TLR) agonists drive hematopoietic stem and progenitor cells (HSPCs) to differentiate along the myeloid lineage in vitro and also in vivo following infection. In this study, we used an in vitro model of HSPC differentiation to investigate the functional consequences (cytokine production) that exposing HSPCs to various pathogen-associated molecular patterns (PAMPs) and Candida albicans cells have on the subsequently derived macrophages. Mouse HSPCs (Lin– cells) were cultured with GM-CSF to induce macrophage differentiation in the presence or absence of the following pattern recognition receptor (PRR) agonists: Pam3CSK4 (TLR2 ligand), LPS (TLR4 ligand), depleted zymosan (which only activates Dectin-1),… More >

  • Open Access

    ARTICLE

    Simvastatin Inhibits the Proliferation and Apoptosis of Macrophages Induced by Mechanical and/or Oxidized Low-Density Lipoprotein

    Kefeng Liu1,2, §, Zhengyu Zhang1,3, §, Ting Pei1, Ziqing Li4, Jingjing Wang1, Hong Wang1, Suning Ping1, Lie Deng1, Linli Wang1, Jintao Huang5, Puyi Sheng4, Shuying Liu1, Chaohong Li1

    Molecular & Cellular Biomechanics, Vol.14, No.2, pp. 101-123, 2017, DOI:10.3970/mcb.2017.014.099

    Abstract This study was designed to investigate the effects of mechanical (MS) and/or oxidized low-density lipoprotein on proliferation and apoptosis of RAW264.7 macrophages and the underlying mechanisms. The cultured quiescent RAW264.7 macrophages were subject to stimulation with MS and/or in the presence or absence of simvastatin and then harvested for Western blot, and immunoflourecence. Either MS or alone could cause increase in cell proliferation and apoptosis, while their combination led to an additive effect. In terms of mechanisms, MS and/or significantly increased phosphorylation levels of MAPKs (ERKs, JNKs and p38MAPK), promoted the reactive oxygen species (ROS) More >

  • Open Access

    ARTICLE

    Extracellular Mg concentration and Ca blockers modulate the initial steps of the response of Th2 lymphocytes in co-culture with macrophages and dendritic cells

    Patrycja Libako1, Julia Miller1, Wojciech Nowacki1, Sara Castiglioni2, Jeanette A. Maier2, Andrzej Mazur3

    European Cytokine Network, Vol.26, No.1, pp. 1-9, 2015, DOI:10.1684/ecn.2015.0361

    Abstract Magnesium is highly involved in the metabolic network such that even subtle disturbances in its homeostasis affect many cellular functions, including calcium homeostasis, signal transduction, energy metabolism, membrane stability and cell proliferation. Recently, magnesium level has been proposed to modulate the priming and activity of immune cells. We studied the behavior of antigen-presenting cells (APCs) and T lymphocytes after altering the magnesium/calcium balance. We used two different populations of primary APCs, i.e. bone marrow-derived dendritic cells and bone marrow-derived macrophages, while D10.G4.1 cells served as a model of responding Th2 cells. Our principal findings are More >

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