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Cidea improves the metabolic profile through expansion of adipose tissue

Abreu-Vieira, Gustavo (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Fischer, Alexander W. (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut,University of Hamburg, Germany
Mattsson, Charlotte (author)
Karolinska Institutet
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de Jong, Jasper M. A. (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Shabalina, Irina G. (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Ryden, Mikael (author)
Karolinska Institutet
Laurencikiene, Jurga (author)
Karolinska Institutet
Arner, Peter (author)
Karolinska Institutet
Cannon, Barbara (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Nedergaard, Jan (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
Petrovic, Natasa (author)
Stockholms universitet,Institutionen för molekylär biovetenskap, Wenner-Grens institut
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 (creator_code:org_t)
2015-06-29
2015
English.
In: Nature Communications. - : Springer Science and Business Media LLC. - 2041-1723. ; 6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • In humans, Cidea (cell death-inducing DNA fragmentation factor alpha-like effector A) is highly but variably expressed in white fat, and expression correlates with metabolic health. Here we generate transgenic mice expressing human Cidea in adipose tissues (aP2-hCidea mice) and show that Cidea is mechanistically associated with a robust increase in adipose tissue expandability. Under humanized conditions (thermoneutrality, mature age and prolonged exposure to high-fat diet), aP2-hCidea mice develop a much more pronounced obesity than their wild-type littermates. Remarkably, the malfunctioning of visceral fat normally caused by massive obesity is fully overcome-perilipin 1 and Akt expression are preserved, tissue degradation is prevented, macrophage accumulation is decreased and adiponectin expression remains high. Importantly, the aP2-hCidea mice display enhanced insulin sensitivity. Our data establish a functional role for Cidea and suggest that, in humans, the association between Cidea levels in white fat and metabolic health is not only correlative but also causative.

Subject headings

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

Keyword

fysiologi
Physiology

Publication and Content Type

ref (subject category)
art (subject category)

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