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Inhibition of TTR aggregation-induced cell death : a new role for serum amyloid P component

Andersson, Karin (author)
Pokrzywa, M (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin,Institute of Biomedicine
Dacklin, Ingrid (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
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Lundgren, Erik (author)
Umeå universitet,Institutionen för molekylärbiologi (Medicinska fakulteten)
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 (creator_code:org_t)
2013-02-04
2013
English.
In: PLOS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 8:2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Serum amyloid P component (SAP) is a glycoprotein that is universally found associated with different types of amyloid deposits. It has been suggested that it stabilizes amyloid fibrils and therefore protects them from proteolytic degradation.METHODOLOGY/PRINCIPAL FINDINGS: In this paper, we show that SAP binds not only to mature amyloid fibrils but also to early aggregates of amyloidogenic mutants of the plasma protein transthyretin (TTR). It does not inhibit fibril formation of TTR mutants, which spontaneously form amyloid in vitro at physiological pH. We found that SAP prevents cell death induced by mutant TTR, while several other molecules that are also known to decorate amyloid fibrils do not have such effect. Using a Drosophila model for TTR-associated amyloidosis, we found a new role for SAP as a protective factor in inhibition of TTR-induced toxicity. Overexpression of mutated TTR leads to a neurological phenotype with changes in wing posture. SAP-transgenic flies were crossed with mutated TTR-expressing flies and the results clearly confirmed a protective effect of SAP on TTR-induced phenotype, with an almost complete reduction in abnormal wing posture. Furthermore, we found in vivo that binding of SAP to mutated TTR counteracts the otherwise detrimental effects of aggregation of amyloidogenic TTR on retinal structure.CONCLUSIONS/SIGNIFICANCE: Together, these two approaches firmly establish the protective effect of SAP on TTR-induced cell death and degenerative phenotypes, and suggest a novel role for SAP through which the toxicity of early amyloidogenic aggregates is attenuated.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Keyword

Serum amyloid P component
transthyretin
familial amyloid polyneuropathy
cell death
neuroblastoma
drosophila
molekylärbiologi
Molecular Biology
Medical Cell Biology
medicinsk cellbiologi
Serum amyloid P component
transthyretin
amyloid
Familial amyloid polyneuropathy
cell death
drosophila
neuroblastoma

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ref (subject category)
art (subject category)

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Andersson, Karin
Pokrzywa, M
Dacklin, Ingrid
Lundgren, Erik
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Cell and Molecul ...
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
NATURAL SCIENCES
NATURAL SCIENCES
and Biological Scien ...
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PLOS ONE
By the university
Umeå University
University of Gothenburg

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