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  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00018-023-04745-4.

Title:
Inhibition of LXR controls the polarization of human inflammatory macrophages through upregulation of MAFB | Cellular and Molecular Life Sciences
Description:
Monocyte-derived macrophages contribute to pathogenesis in inflammatory diseases and their effector functions greatly depend on the prevailing extracellular milieu. Whereas M-CSF primes macrophages for acquisition of an anti-inflammatory profile, GM-CSF drives the generation of T cell-stimulatory and pro-inflammatory macrophages. Liver X Receptors (LXRα and LXRβ) are nuclear receptors that control cholesterol metabolism and regulate differentiation of tissue-resident macrophages. Macrophages from rheumatoid arthritis and other inflammatory pathologies exhibit an enriched LXR pathway, and recent reports have shown that LXR activation raises pro-inflammatory effects and impairs the acquisition of the anti-Inflammatory profile of M-CSF-dependent monocyte-derived macrophages (M-MØ). We now report that LXR inhibition prompts the acquisition of an anti-inflammatory gene and functional profile of macrophages generated within a pathological environment (synovial fluid from Rheumatoid Arthritis patients) as well as during the GM-CSF-dependent differentiation of human monocyte-derived macrophages (GM-MØ). Mechanistically, inhibition of LXR results in macrophages with higher expression of the v-Maf Avian Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (MAFB) transcription factor, which governs the macrophage anti-inflammatory profile, as well as over-expression of MAFB-regulated genes. Indeed, gene silencing experiments on human macrophages evidenced that MAFB is required for the LXR inhibitor to enhance the anti-inflammatory nature of human macrophages. As a whole, our results demonstrate that LXR inhibition prompts the acquisition of an anti-inflammatory transcriptional and functional profile of human macrophages in a MAFB-dependent manner, and propose the use of LXR antagonists as potential therapeutic alternatives in macrophage re-programming strategies during inflammatory responses.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

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Keywords {🔍}

macrophages, lxr, pubmed, article, google, scholar, cas, macrophage, expression, genes, fig, mafb, inhibition, gene, human, gmmø, antiinflammatory, gskgmmø, proinflammatory, inflammatory, profile, central, arthritis, synovial, rheumatoid, gsk, gskrasfmø, differentiation, cell, monocytes, activation, immunol, liver, monocytederived, gmcsf, levels, gse, enrichment, supplementary, rasfmø, acquisition, mmø, generated, factor, independent, analysis, polarization, shown, results, protein,

Topics {✒️}

gm-csf-dependent monocyte-derived gm-mø m-csf-dependent monocyte-derived macrophages granulocyte-macrophage colony-stimulating factor albeit gw/gsk-gm-mø exhibited monocyte-derived pro-inflammatory gm-mø ox-ldl-dependent trained immunity macrophage-deficient op/op mouse gw/gsk-gm-mø produced significantly quantitative real-time rt-pcr macrophage-csf-dependent macrophage responses generate gm-csf-polarized macrophages pid2019-104284rb-i00/aei/https gsk-gm-mø greatly coincided murine collagen-induced arthritis uk/arrayexpress/experiments/e-mtab-8322/ gm-mø-specific gene sets gm-mø-specific genes egln3 pro-inflammatory tlr4 signaling maría teresa schiaffino pro-inflammatory gm-mø transcriptomes gm-csf-driven monocyte article download pdf gsk-gm-mø gene profile monocyte-derived m-mø [48] human monocyte-derived macrophages transcription factor c-maf colony-stimulating factor 1 post-hoc tukey test real-time quantitative pcr broad-spectrum therapeutic suppression anti-inflammatory gene set pro-inflammatory gene set gm-csf-dependent macrophages srebp-dependent gene sets m-csf-polarized macrophages macrophage anti-inflammatory polarization gm-csf-dependent differentiation m-csf-induced macrophages gsk-gm-mø exhibited r-package deseq2 algorithms characterizes tissue-resident macrophages m-csf primes macrophages rheumatoid arthritis synovial fluid promote macrophage pro-inflammatory anti-inflammatory m-mø anti-inflammatory m-mø [23 anti-inflammatory macrophage markers fast gapped-read alignment pro-inflammatory m-mø gm-csf primes macrophages

Schema {🗺️}

WebPage:
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         headline:Inhibition of LXR controls the polarization of human inflammatory macrophages through upregulation of MAFB
         description:Monocyte-derived macrophages contribute to pathogenesis in inflammatory diseases and their effector functions greatly depend on the prevailing extracellular milieu. Whereas M-CSF primes macrophages for acquisition of an anti-inflammatory profile, GM-CSF drives the generation of T cell-stimulatory and pro-inflammatory macrophages. Liver X Receptors (LXRα and LXRβ) are nuclear receptors that control cholesterol metabolism and regulate differentiation of tissue-resident macrophages. Macrophages from rheumatoid arthritis and other inflammatory pathologies exhibit an enriched LXR pathway, and recent reports have shown that LXR activation raises pro-inflammatory effects and impairs the acquisition of the anti-Inflammatory profile of M-CSF-dependent monocyte-derived macrophages (M-MØ). We now report that LXR inhibition prompts the acquisition of an anti-inflammatory gene and functional profile of macrophages generated within a pathological environment (synovial fluid from Rheumatoid Arthritis patients) as well as during the GM-CSF-dependent differentiation of human monocyte-derived macrophages (GM-MØ). Mechanistically, inhibition of LXR results in macrophages with higher expression of the v-Maf Avian Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (MAFB) transcription factor, which governs the macrophage anti-inflammatory profile, as well as over-expression of MAFB-regulated genes. Indeed, gene silencing experiments on human macrophages evidenced that MAFB is required for the LXR inhibitor to enhance the anti-inflammatory nature of human macrophages. As a whole, our results demonstrate that LXR inhibition prompts the acquisition of an anti-inflammatory transcriptional and functional profile of human macrophages in a MAFB-dependent manner, and propose the use of LXR antagonists as potential therapeutic alternatives in macrophage re-programming strategies during inflammatory responses.
         datePublished:2023-03-17T00:00:00Z
         dateModified:2023-03-17T00:00:00Z
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         license:http://creativecommons.org/licenses/by/4.0/
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            Inflammation
            Innate immunity
            Macrophage Polarization
            Transcriptional profile
            Cell Biology
            Biomedicine
            general
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            Biochemistry
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      headline:Inhibition of LXR controls the polarization of human inflammatory macrophages through upregulation of MAFB
      description:Monocyte-derived macrophages contribute to pathogenesis in inflammatory diseases and their effector functions greatly depend on the prevailing extracellular milieu. Whereas M-CSF primes macrophages for acquisition of an anti-inflammatory profile, GM-CSF drives the generation of T cell-stimulatory and pro-inflammatory macrophages. Liver X Receptors (LXRα and LXRβ) are nuclear receptors that control cholesterol metabolism and regulate differentiation of tissue-resident macrophages. Macrophages from rheumatoid arthritis and other inflammatory pathologies exhibit an enriched LXR pathway, and recent reports have shown that LXR activation raises pro-inflammatory effects and impairs the acquisition of the anti-Inflammatory profile of M-CSF-dependent monocyte-derived macrophages (M-MØ). We now report that LXR inhibition prompts the acquisition of an anti-inflammatory gene and functional profile of macrophages generated within a pathological environment (synovial fluid from Rheumatoid Arthritis patients) as well as during the GM-CSF-dependent differentiation of human monocyte-derived macrophages (GM-MØ). Mechanistically, inhibition of LXR results in macrophages with higher expression of the v-Maf Avian Musculoaponeurotic Fibrosarcoma Oncogene Homolog B (MAFB) transcription factor, which governs the macrophage anti-inflammatory profile, as well as over-expression of MAFB-regulated genes. Indeed, gene silencing experiments on human macrophages evidenced that MAFB is required for the LXR inhibitor to enhance the anti-inflammatory nature of human macrophages. As a whole, our results demonstrate that LXR inhibition prompts the acquisition of an anti-inflammatory transcriptional and functional profile of human macrophages in a MAFB-dependent manner, and propose the use of LXR antagonists as potential therapeutic alternatives in macrophage re-programming strategies during inflammatory responses.
      datePublished:2023-03-17T00:00:00Z
      dateModified:2023-03-17T00:00:00Z
      pageStart:1
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      license:http://creativecommons.org/licenses/by/4.0/
      sameAs:https://doi.org/10.1007/s00018-023-04745-4
      keywords:
         Inflammation
         Innate immunity
         Macrophage Polarization
         Transcriptional profile
         Cell Biology
         Biomedicine
         general
         Life Sciences
         Biochemistry
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                  name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
                  address:
                     name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
                     type:PostalAddress
                  type:Organization
            type:Person
            name:María Teresa Schiaffino
            affiliation:
                  name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
                  address:
                     name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
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                  address:
                     name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
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                  name:CSIC
                  address:
                     name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
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                  address:
                     name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
                     type:PostalAddress
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            name:Amaya Puig-Kröger
            affiliation:
                  name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
                  address:
                     name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
                     type:PostalAddress
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            name:Antonio Castrillo
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                  name:Universidad de Las Palmas de Gran Canaria
                  address:
                     name:Unidad de Biomedicina (Unidad Asociada al CSIC), Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Investigación Medio Ambiente y Salud, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain
                     type:PostalAddress
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                  name:Centro Mixto Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid (CSIC-UAM)
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                     name:Instituto Investigaciones Biomédicas “Alberto Sols” (IIBM), Centro Mixto Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Ángel L. Corbí
            url:http://orcid.org/0000-0003-1980-5733
            affiliation:
                  name:CSIC
                  address:
                     name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
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      name:Cellular and Molecular Life Sciences
      issn:
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      volumeNumber:80
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      name:Springer International Publishing
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      name:Mónica Torres-Torresano
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            name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
            address:
               name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
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      name:María Teresa Schiaffino
      affiliation:
            name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
            address:
               name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
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            name:CSIC
            address:
               name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Bárbara Alonso
      affiliation:
            name:CSIC
            address:
               name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Miguel A. Vega
      affiliation:
            name:CSIC
            address:
               name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Amaya Puig-Kröger
      affiliation:
            name:Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón
            address:
               name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Antonio Castrillo
      affiliation:
            name:Universidad de Las Palmas de Gran Canaria
            address:
               name:Unidad de Biomedicina (Unidad Asociada al CSIC), Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Investigación Medio Ambiente y Salud, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain
               type:PostalAddress
            type:Organization
            name:Centro Mixto Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid (CSIC-UAM)
            address:
               name:Instituto Investigaciones Biomédicas “Alberto Sols” (IIBM), Centro Mixto Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Ángel L. Corbí
      url:http://orcid.org/0000-0003-1980-5733
      affiliation:
            name:CSIC
            address:
               name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
      name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
      name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain
      name:Unidad de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain
      name:Unidad de Biomedicina (Unidad Asociada al CSIC), Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Investigación Medio Ambiente y Salud, Universidad de Las Palmas de Gran Canaria, Las Palmas, Spain
      name:Instituto Investigaciones Biomédicas “Alberto Sols” (IIBM), Centro Mixto Consejo Superior de Investigaciones Científicas y Universidad Autónoma de Madrid (CSIC-UAM), Madrid, Spain
      name:Myeloid Cell Laboratory, Centro de Investigaciones Biológicas, CSIC, Madrid, Spain

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