The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Amyloid-β peptide activates cultured astrocytes: morphological alterations, cytokine induction and nitric oxide release
Abstract
A common feature of many neurodegenerative disorders is an abundance of activated glial cells (astrocytes and microglia). In Alzheimer's disease (AD), activated astrocytes are in close apposition to and surrounding the amyloid plaques. The mechanisms by which the astrocytes become activated in AD and the consequences of reactive astrocytosis to disease progression are not known. We examined the possibility that the amyloid-beta (Abeta) peptide, a major constituent of the amyloid plaque, could act as a stimulus leading to activation. We found that treatment of rat cortical astrocyte cultures with aggregated Abeta 1-42 peptide induces activation, as assessed by reactive morphological changes and upregulation of selective glial mRNA and proteins, such as the inflammatory cytokine interleukin-1beta. Abeta also stimulates inducible nitric oxide synthase (iNOS) mRNA levels and nitric oxide (NO) release. Abeta 1-42, a major form of amyloid associated with neurotoxicity, activated astrocytes in a time- and dose-dependent manner, whereas a scrambled Abeta 1-42 sequence or Abeta 17-42 had little or no effect. We also determined that the Abeta activity can be found in a supernatant fraction containing soluble Abeta oligomers. Our data suggest that Abeta plays a role in the reactive astrocytosis of AD and that the inflammatory response induced upon glial activation is a critical component of the neurodegenerative process.
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“A 1-42 aged according to this protocol is a mixture of fibrils and soluble globular aggregates, and is active to astrocytes (37,38) and toxic to neurons (26,27).”
From Apolipoprotein E Receptors Mediate the Effects of β-Amyloid on Astrocyte Cultures (2000) · cites this paper as [37]
In the citing paper
“We have previously demonstrated (37) that aged preparations of A 1-42 induce activation of primary rat astrocyte cultures, as measured by changes in morphology and an increase in IL-1 mRNA.”
From Apolipoprotein E Receptors Mediate the Effects of β-Amyloid on Astrocyte Cultures (2000) · cites this paper as [37]
In the citing paper
“In agreement with our previous report (37), the GFAP levels did not change upon activation (Fig. 1C).”
From Apolipoprotein E Receptors Mediate the Effects of β-Amyloid on Astrocyte Cultures (2000) · cites this paper as [37]
In the citing paper
“As previously reported (37,41) these tertiary cultures are ϳ95-98% astrocytes, with only ϳ2-5% microglial cells.”
From Apolipoprotein E Receptors Mediate the Effects of β-Amyloid on Astrocyte Cultures (2000) · cites this paper as [37]
Citations
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Metadata
- Authors
- Hu, J., Akama, K. T., Krafft, G. A., Chromy, B. A., & Van Eldik, L. J.
- Venue
- Brain Research
- Publisher
- Elsevier BV
- Published
- 1998-03
- Volume
- 785
- Issue
- 2
- Pages
- 195-206
- ISSN
- 0006-8993
- Cited by
- 262
- References
- 4
- Language
- en
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