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We are analyzing https://link.springer.com/article/10.1007/s00401-002-0569-x.

Title:
Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process | Acta Neuropathologica
Description:
Tau-immunoreactive astrocytes in progressive supranuclear palsy (PSP) have a distinctive morphology and are referred to as tufted astrocytes (TA). We hypothesized that TA may be a degenerative change in reactive astrocytes. To test this hypothesis we examined the relationship of TA to gliosis in PSP. We first examined the distribution of gliosis [glial fibrillary acid protein (GFAP)-positive astrocytes], TA, neurofibrillary tangles (NFT) and pretangles in brain sections of neuropathologically pure PSP cases. Second, we examined PSP cases complicated by infarcts or Alzheimer
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Mobile Technology & AI
  • Social Networks
  • Politics

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 7,734,772 visitors per month in the current month.

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

The income method remains a mystery to us.

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 might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

astrocytes, article, tau, gliosis, progressive, supranuclear, palsy, reactive, psp, access, privacy, cookies, content, information, publish, search, accumulation, degenerative, distribution, glial, nft, cases, open, august, data, log, journal, research, acta, process, togo, dickson, examined, lesions, discover, springer, optional, personal, parties, policy, change, find, track, neuropathologica, cite, takashi, dennis, explore, tufted, protein,

Topics {✒️}

month download article/chapter progressive supranuclear palsy takashi togo & dennis related subjects full article pdf privacy choices/manage cookies neurofibrillary tangles β-amyloid protein tau-immunoreactive astrocytes check access instant access european economic area article togo conditions privacy policy accepting optional cookies tufted astrocytes tau accumulation main content log journal finder publish article log disease acta neuropathol 104 article cite privacy policy personal data brain sections books a reactive process information optional cookies manage preferences reactive astrocytes gliosis prominent gliosis paralleled data protection essential cookies cookies skip subscription content similar content institution subscribe journal publish positive astrocytes] usage analysis social media varying standards october 2002 volume 104 distinctive morphology double immunostaining tau triple immunostaining

Schema {🗺️}

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         headline:Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process
         description: Tau-immunoreactive astrocytes in progressive supranuclear palsy (PSP) have a distinctive morphology and are referred to as tufted astrocytes (TA). We hypothesized that TA may be a degenerative change in reactive astrocytes. To test this hypothesis we examined the relationship of TA to gliosis in PSP. We first examined the distribution of gliosis [glial fibrillary acid protein (GFAP)-positive astrocytes], TA, neurofibrillary tangles (NFT) and pretangles in brain sections of neuropathologically pure PSP cases. Second, we examined PSP cases complicated by infarcts or Alzheimer's disease, since these cases would have reactive astrocytes associated with lesions. We used double immunostaining for GFAP and tau for cases with vascular lesions, and triple immunostaining for GFAP, tau and β-amyloid protein for sections with senile plaques. There was no correlation between the distribution of gliosis and TA, with gliosis prominent in globus pallidus and subthalamic nucleus, and TA prominent in motor cortex and striatum. On the other hand, gliosis paralleled the distribution of NFT, but not the distribution of pretangles, suggesting that NFT contributes to gliosis in PSP. Although reactive astrocytes were present around infarcts and senile plaques, TA were not associated with these lesions. Tau accumulation in astrocytes in PSP was not preferential to (and was actually independent of) reactive astrocytes. This is consistent with the notion that tau accumulation in astrocytes is a degenerative rather than reactive process. Unlike NFT, astrocytic degeneration does not seem to contribute to gliosis or neuronal loss in PSP, and its clinical significance remains unclear.
         datePublished:
         dateModified:
         pageStart:398
         pageEnd:402
         sameAs:https://doi.org/10.1007/s00401-002-0569-x
         keywords:
            Progressive supranuclear palsy Tufted astrocytes Gliosis Neurofibrillary tangles
            Pathology
            Neurosciences
         image:
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            name:Acta Neuropathologica
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               name:Takashi Togo
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                        name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
                        type:PostalAddress
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               name:Dennis W. Dickson
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                     name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
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                        name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
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      headline:Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process
      description: Tau-immunoreactive astrocytes in progressive supranuclear palsy (PSP) have a distinctive morphology and are referred to as tufted astrocytes (TA). We hypothesized that TA may be a degenerative change in reactive astrocytes. To test this hypothesis we examined the relationship of TA to gliosis in PSP. We first examined the distribution of gliosis [glial fibrillary acid protein (GFAP)-positive astrocytes], TA, neurofibrillary tangles (NFT) and pretangles in brain sections of neuropathologically pure PSP cases. Second, we examined PSP cases complicated by infarcts or Alzheimer's disease, since these cases would have reactive astrocytes associated with lesions. We used double immunostaining for GFAP and tau for cases with vascular lesions, and triple immunostaining for GFAP, tau and β-amyloid protein for sections with senile plaques. There was no correlation between the distribution of gliosis and TA, with gliosis prominent in globus pallidus and subthalamic nucleus, and TA prominent in motor cortex and striatum. On the other hand, gliosis paralleled the distribution of NFT, but not the distribution of pretangles, suggesting that NFT contributes to gliosis in PSP. Although reactive astrocytes were present around infarcts and senile plaques, TA were not associated with these lesions. Tau accumulation in astrocytes in PSP was not preferential to (and was actually independent of) reactive astrocytes. This is consistent with the notion that tau accumulation in astrocytes is a degenerative rather than reactive process. Unlike NFT, astrocytic degeneration does not seem to contribute to gliosis or neuronal loss in PSP, and its clinical significance remains unclear.
      datePublished:
      dateModified:
      pageStart:398
      pageEnd:402
      sameAs:https://doi.org/10.1007/s00401-002-0569-x
      keywords:
         Progressive supranuclear palsy Tufted astrocytes Gliosis Neurofibrillary tangles
         Pathology
         Neurosciences
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            name:Takashi Togo
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                  name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
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                     name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
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            name:Dennis W. Dickson
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                  name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
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                     name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
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               name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
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      name:Dennis W. Dickson
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            name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA
            address:
               name:Departments of Pathology (Neuropathology) and Neuroscience, Birdsall 317, Mayo Clinic, Jacksonville, 4500 San Pablo Road, Jacksonville, FL 32224, USA,
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External Links {🔗}(27)

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