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Adipocyte-specific disruption of mouse Cnot3 causes lipodystrophy.
Li, Xue; Morita, Masahiro; Kikuguchi, Chisato; Takahashi, Akinori; Suzuki, Toru; Yamamoto, Tadashi.
Affiliation
  • Li X; Cell Signal Unit, Okinawa Institute of Science and Technology Graduate University, Japan.
  • Morita M; Department of Biochemistry, Goodman Cancer Research Centre, McGill University, Montreal, Canada.
  • Kikuguchi C; Cell Signal Unit, Okinawa Institute of Science and Technology Graduate University, Japan.
  • Takahashi A; Laboratory for Immunogenetics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Suzuki T; Cell Signal Unit, Okinawa Institute of Science and Technology Graduate University, Japan.
  • Yamamoto T; Cell Signal Unit, Okinawa Institute of Science and Technology Graduate University, Japan.
FEBS Lett ; 591(2): 358-368, 2017 01.
Article in En | MEDLINE | ID: mdl-28032897
Lipodystrophy involves a loss of adipose tissue. In mice, disruption of adipose tissue Cnot3, a subunit of the CCR4-NOT deadenylase complex, causes adipose tissue anomalies. In Cnot3ad-/- mice, white adipose tissue (WAT) decreases concomitantly with enhanced inflammation, whereas brown adipose tissue increases and contains larger lipid droplets. Cnot3ad-/- mice show hyperinsulinemia, hyperglycemia, insulin resistance, and glucose intolerance, and cannot maintain body temperature during cold exposure. Increased expression of inflammatory genes and decreased leptin expression also occur in Cnot3ad-/- WAT, achieving levels similar to those in lipodystrophic aP2-nSrebp1c and Ppargldi/+ mice; thus, Cnot3ad-/- mice exhibit lipodystrophy.
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Full text: 1 Database: MEDLINE Main subject: Transcription Factors / Adipocytes / Lipodystrophy Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Journal: FEBS Lett Year: 2017 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Main subject: Transcription Factors / Adipocytes / Lipodystrophy Type of study: Etiology_studies / Prognostic_studies Limits: Animals Language: En Journal: FEBS Lett Year: 2017 Type: Article Affiliation country: Japan