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DOI . ORG {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Doi.org Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
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We began analyzing https://link.springer.com/chapter/10.1007/978-3-319-07320-0_9, but it redirected us to https://link.springer.com/chapter/10.1007/978-3-319-07320-0_9. The analysis below is for the second page.

Title[redir]:
Serotonin Modulation of Macrophage Polarization: Inflammation and Beyond | SpringerLink
Description:
Macrophages display a ample plethora of effector functions whose acquisition is promoted by the surrounding cytokine and cellular environment. Depending on the stimulus, macrophages become specialized (“polarized”) for either pathogen elimination, tissue...

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Business & Finance

Content Management System {📝}

What CMS is doi.org built with?

Custom-built

No common CMS systems were detected on Doi.org, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of doi.org 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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Doi.org Make Money? {💸}

We find it hard to spot revenue streams.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Doi.org might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

pubmed, google, scholar, cas, central, serotonin, macrophages, macrophage, receptor, immunol, cells, cancer, cell, polarization, human, receptors, activation, med, res, htb, nat, inflammation, immune, blood, tumor, factor, role, sci, pharmacol, expression, rev, liver, clin, tissue, inflammatory, immunity, biol, chem, chapter, mantovani, tumorassociated, mice, invest, regulation, growth, functions, responses, gene, dendritic, system,

Topics {✒️}

ccaat/enhancer-binding protein beta granulocyte-macrophage colony-stimulating factor human m-csf-generated macrophages 5-ht7-receptor-mediated gastric relaxation macrophage-csf-dependent macrophage responses chemotherapy drug-induced apoptosis transforming growth factor-beta1 m2 anti-inflammatory/regulatory macrophages macrophage colony-stimulating factor structure-activity relationship study lipopolysaccharide-induced gene activation serotonin-selective antidepressant actions 5-ht7 receptor-mediated relaxation month download article/chapter t-cell priming capacity lps-primed human monocytes serum-free tissue culture anti-inflammatory macrophage markers muscle layer-dependent manner selective serotonin-reuptake inhibitors central nervous system ras-dependent erk activation lps-induced il-10 release cytokine-driven compensatory proliferation enhanced irf-3/stat1 activation high-affinity serotonin receptor enhance t-cell activation adipocyte-derived th2 cytokines antiapoptotic mediator sphingosine-1-phosphate g-protein signal transduction resolution-phase macrophages possess cytokine-induced sickness behaviour central 5-ht7 receptors serotonin/5-ht2b receptor signaling macrophage-csf dependent nebigil cg 5-hydroxytryptamine induced relaxation tumor-induced immune suppression receptor gene products anti-inflammatory state van ginderachter ja m-csf origin interferon-gamma induced phagocytosis palsson-mcdermott em phosphatidylinositol-specific phospholipase privacy choices/manage cookies 5-ht7 receptor research differential macrophage programming primary pulmonary hypertension skews macrophage polarization

Questions {❓}

  • 5-HT2B Receptor on Macrophages: What for?
  • Functional consequence of serotonin/5-HT2B receptor signaling in heart: role of mitochondria in transition between hypertrophy and heart failure?
  • Serotonin: a double-edged sword for the liver?

Schema {🗺️}

ScholarlyArticle:
      headline:Serotonin Modulation of Macrophage Polarization: Inflammation and Beyond
      pageEnd:115
      pageStart:89
      image:https://media.springernature.com/w153/springer-static/cover/book/978-3-319-07320-0.jpg
      genre:
         Biomedical and Life Sciences
         Biomedical and Life Sciences (R0)
      isPartOf:
         name:Oxidative Stress and Inflammation in Non-communicable Diseases - Molecular Mechanisms and Perspectives in Therapeutics
         isbn:
            978-3-319-07320-0
            978-3-319-07319-4
         type:Book
      publisher:
         name:Springer International Publishing
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Mateo de las Casas-Engel
            affiliation:
                  name:Consejo Superior de Investigaciones Científicas (CSIC)
                  address:
                     name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Angel L. Corbí
            affiliation:
                  name:Consejo Superior de Investigaciones Científicas (CSIC)
                  address:
                     name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      keywords:Inflammation, Macrophages, Psychiatric diseases, Serotonin, Serotonin receptor
      description:Macrophages display a ample plethora of effector functions whose acquisition is promoted by the surrounding cytokine and cellular environment. Depending on the stimulus, macrophages become specialized (“polarized”) for either pathogen elimination, tissue repair and wound healing or immunosuppression. This “polarization” versatility allows macrophages to critically contribute to tissue homeostasis, as they promote initiation and resolution of inflammatory responses. As a consequence, deregulation of the tissue macrophage polarization balance is an etiological agent of chronic inflammation, autoimmune diseases, cancer and even obesity and insulin resistance. In the present review we describe current concepts on the molecular basis and the patho-physiological implications of macrophage polarization, and describe its modulation by serotonin (5-HT), a neurotransmitter that regulates inflammation and tissue repair via a large set of receptors (5-HTR1-7). 5-HT modulates the phenotypic and functional polarization of macrophages, and contributes to the maintenance of an anti-inflammatory state mainly via 5-HTR2B and 5-HTR7, whose activation has a great impact on macrophage gene expression profile. The identification of 5-HTR2B and 5-HTR7 as functionally-relevant polarization markers suggests their therapeutic value in inflammatory pathologies as well as their potential involvement in linking the immune and nervous systems.
      datePublished:2014
      isAccessibleForFree:
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         cssSelector:.main-content
         type:WebPageElement
      context:https://schema.org
Book:
      name:Oxidative Stress and Inflammation in Non-communicable Diseases - Molecular Mechanisms and Perspectives in Therapeutics
      isbn:
         978-3-319-07320-0
         978-3-319-07319-4
Organization:
      name:Springer International Publishing
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Consejo Superior de Investigaciones Científicas (CSIC)
      address:
         name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
         type:PostalAddress
      name:Consejo Superior de Investigaciones Científicas (CSIC)
      address:
         name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Mateo de las Casas-Engel
      affiliation:
            name:Consejo Superior de Investigaciones Científicas (CSIC)
            address:
               name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
               type:PostalAddress
            type:Organization
      name:Angel L. Corbí
      affiliation:
            name:Consejo Superior de Investigaciones Científicas (CSIC)
            address:
               name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
      name:Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {🔗}(776)

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