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LINK . SPRINGER . COM {}

  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
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1186/s12979-021-00215-2.

Title:
Macrophage function in the elderly and impact on injury repair and cancer | Immunity & Ageing
Description:
Older age is associated with deteriorating health, including escalating risk of diseases such as cancer, and a diminished ability to repair following injury. This rise in age-related diseases/co-morbidities is associated with changes to immune function, including in myeloid cells, and is related to immunosenescence. Immunosenescence reflects age-related changes associated with immune dysfunction and is accompanied by low-grade chronic inflammation or inflammageing. This is characterised by increased levels of circulating pro-inflammatory cytokines such as tumor necrosis factor (TNF), interleukin (IL)-1β and IL-6. However, in healthy ageing, there is a concomitant age-related escalation in anti-inflammatory cytokines such as transforming growth factor-β1 (TGF-β1) and IL-10, which may overcompensate to regulate the pro-inflammatory state. Key inflammatory cells, macrophages, play a role in cancer development and injury repair in young hosts, and we propose that their role in ageing in these scenarios may be more profound. Imbalanced pro- and anti-inflammatory factors during ageing may also have a significant influence on macrophage function and further impact the severity of age-related diseases in which macrophages are known to play a key role. In this brief review we summarise studies describing changes to inflammatory function of macrophages (from various tissues and across sexes) during healthy ageing. We also describe age-related diseases/co-morbidities where macrophages are known to play a key role, focussed on injury repair processes and cancer, plus comment briefly on strategies to correct for these age-related changes.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We can't figure out the monetization strategy.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

pubmed, article, macrophages, google, scholar, cas, central, mice, cells, macrophage, ageing, cell, aged, elderly, function, cancer, aging, immunol, immune, studies, injury, tumor, agerelated, young, muscle, proinflammatory, repair, inflammatory, cblj, months, response, tissue, female, increased, monocytes, mdscs, bone, responses, inflammation, factors, humans, shown, skeletal, immunity, impact, increase, healthy, growth, role, due,

Topics {✒️}

young serum/plasma/blood products diet-induced murine steatohepatitis article download pdf female c57bl/6j mice c57bl/6j female mice chronic age-related diseases c57bl/6j geriatric mice describe age-related diseases/ female c57bl/6n mice muscle-derived nitric oxide aged c57bl/6j mice tumor-bearing mice led bone marrow-derived monocytes/macrophages myeloid-derived suppressor cell serum/plasma/blood products concomitant age-related escalation age-related thymic involution myeloid‐derived suppressor cells myeloid-derived suppressor cells pre-activated basal state interferon-gamma inducible protein-10 young tumor-bearing mice low-grade chronic inflammation transforming growth factor-β1 macrophage-specific scavenger receptor nf-kappab-dependent mechanism hif-1alpha regulates function reflecting age-related differences older hip-fracture patients bone marrow-derived macrophages bone-marrow derived macrophages brain-resident microglial populations van den bossche circulating pro-inflammatory cytokines reduces treatment-induced cachexia tumor necrosis factor janus kinase/signal transducers targeting macrophage-recruiting chemokines bone-fracture healing model injury-induced microglia behavior c57bl/6j mice pro-resolving monocyte/macrophages reduced anti-oxidative defense age-related diseases/ age-related diseases regulatory t-cell populations immunosenescence reflects age-related heightened pro-inflammatory phenotype urethane-induced lung carcinogenesis zeh hj 3rd

Questions {❓}

  • Can blocking inflammation enhance immunity during aging?
  • Interleukin-6 myokine signaling in skeletal muscle: a double-edged sword?
  • Macrophage Immunometabolism: Where Are We (Going)?
  • Metabolic Alterations in Aging Macrophages: Ingredients for Inflammaging?
  • Sex differences in obesity, lipid metabolism, and inflammation-A role for the sex chromosomes?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Macrophage function in the elderly and impact on injury repair and cancer
         description:Older age is associated with deteriorating health, including escalating risk of diseases such as cancer, and a diminished ability to repair following injury. This rise in age-related diseases/co-morbidities is associated with changes to immune function, including in myeloid cells, and is related to immunosenescence. Immunosenescence reflects age-related changes associated with immune dysfunction and is accompanied by low-grade chronic inflammation or inflammageing. This is characterised by increased levels of circulating pro-inflammatory cytokines such as tumor necrosis factor (TNF), interleukin (IL)-1β and IL-6. However, in healthy ageing, there is a concomitant age-related escalation in anti-inflammatory cytokines such as transforming growth factor-β1 (TGF-β1) and IL-10, which may overcompensate to regulate the pro-inflammatory state. Key inflammatory cells, macrophages, play a role in cancer development and injury repair in young hosts, and we propose that their role in ageing in these scenarios may be more profound. Imbalanced pro- and anti-inflammatory factors during ageing may also have a significant influence on macrophage function and further impact the severity of age-related diseases in which macrophages are known to play a key role. In this brief review we summarise studies describing changes to inflammatory function of macrophages (from various tissues and across sexes) during healthy ageing. We also describe age-related diseases/co-morbidities where macrophages are known to play a key role, focussed on injury repair processes and cancer, plus comment briefly on strategies to correct for these age-related changes.
         datePublished:2021-01-13T00:00:00Z
         dateModified:2021-01-13T00:00:00Z
         pageStart:1
         pageEnd:11
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s12979-021-00215-2
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            Macrophages
            Age‐related diseases
            Inflammation
            Cancer
            Injury repair
            Immunology
            Geriatrics/Gerontology
            Aging
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            Clinical Nutrition
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            issn:
               1742-4933
            volumeNumber:18
            type:
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                        name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
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         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Macrophage function in the elderly and impact on injury repair and cancer
      description:Older age is associated with deteriorating health, including escalating risk of diseases such as cancer, and a diminished ability to repair following injury. This rise in age-related diseases/co-morbidities is associated with changes to immune function, including in myeloid cells, and is related to immunosenescence. Immunosenescence reflects age-related changes associated with immune dysfunction and is accompanied by low-grade chronic inflammation or inflammageing. This is characterised by increased levels of circulating pro-inflammatory cytokines such as tumor necrosis factor (TNF), interleukin (IL)-1β and IL-6. However, in healthy ageing, there is a concomitant age-related escalation in anti-inflammatory cytokines such as transforming growth factor-β1 (TGF-β1) and IL-10, which may overcompensate to regulate the pro-inflammatory state. Key inflammatory cells, macrophages, play a role in cancer development and injury repair in young hosts, and we propose that their role in ageing in these scenarios may be more profound. Imbalanced pro- and anti-inflammatory factors during ageing may also have a significant influence on macrophage function and further impact the severity of age-related diseases in which macrophages are known to play a key role. In this brief review we summarise studies describing changes to inflammatory function of macrophages (from various tissues and across sexes) during healthy ageing. We also describe age-related diseases/co-morbidities where macrophages are known to play a key role, focussed on injury repair processes and cancer, plus comment briefly on strategies to correct for these age-related changes.
      datePublished:2021-01-13T00:00:00Z
      dateModified:2021-01-13T00:00:00Z
      pageStart:1
      pageEnd:11
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s12979-021-00215-2
      keywords:
         Macrophages
         Age‐related diseases
         Inflammation
         Cancer
         Injury repair
         Immunology
         Geriatrics/Gerontology
         Aging
         Public Health
         Clinical Nutrition
         Antibodies
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs12979-021-00215-2/MediaObjects/12979_2021_215_Fig1_HTML.png
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs12979-021-00215-2/MediaObjects/12979_2021_215_Fig2_HTML.png
      isPartOf:
         name:Immunity & Ageing
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            1742-4933
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         name:BioMed Central
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                     type:PostalAddress
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                     type:PostalAddress
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         name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
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      address:
         name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
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      name:University of Western Australia
      address:
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         type:PostalAddress
      name:University of Western Australia
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         name:School of Human Sciences, University of Western Australia, Nedlands, Australia
         type:PostalAddress
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         name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
         type:PostalAddress
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      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      name:HG Radley
      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      name:B Lee
      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      name:DE Dye
      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      name:FJ Pixley
      affiliation:
            name:University of Western Australia
            address:
               name:School of Biomedical Sciences, University of Western Australia, Nedlands, Australia
               type:PostalAddress
            type:Organization
      name:MD Grounds
      affiliation:
            name:University of Western Australia
            address:
               name:School of Human Sciences, University of Western Australia, Nedlands, Australia
               type:PostalAddress
            type:Organization
      name:DJ Nelson
      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      name:C Jackaman
      affiliation:
            name:Curtin University
            address:
               name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
      name:School of Biomedical Sciences, University of Western Australia, Nedlands, Australia
      name:School of Human Sciences, University of Western Australia, Nedlands, Australia
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia
      name:Curtin Medical School, Curtin Health Innovation Research Institute, Faculty of Health Sciences, Curtin University, Bentley, Australia

External Links {🔗}(509)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

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