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The molecular and metabolic program by which white adipocytes adapt to cool physiologic temperatures.
Mori, Hiroyuki; Dugan, Colleen E; Nishii, Akira; Benchamana, Ameena; Li, Ziru; Cadenhead, Thomas S; Das, Arun K; Evans, Charles R; Overmyer, Katherine A; Romanelli, Steven M; Peterson, Sydney K; Bagchi, Devika P; Corsa, Callie A; Hardij, Julie; Learman, Brian S; El Azzouny, Mahmoud; Coon, Joshua J; Inoki, Ken; MacDougald, Ormond A.
Afiliação
  • Mori H; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Dugan CE; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Nishii A; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Benchamana A; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Li Z; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Cadenhead TS; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Das AK; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Evans CR; Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Overmyer KA; Morgridge Institute for Research, Madison, Wisconsin, United States of America.
  • Romanelli SM; National Center for Quantitative Biology of Complex Systems, Madison, Wisconsin, United States of America.
  • Peterson SK; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Bagchi DP; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Corsa CA; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Hardij J; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Learman BS; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • El Azzouny M; Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.
  • Coon JJ; Agilent Technologies, Inc., Santa Clara, California, United States of America.
  • Inoki K; Morgridge Institute for Research, Madison, Wisconsin, United States of America.
  • MacDougald OA; National Center for Quantitative Biology of Complex Systems, Madison, Wisconsin, United States of America.
PLoS Biol ; 19(5): e3000988, 2021 05.
Article em En | MEDLINE | ID: mdl-33979328
ABSTRACT
Although visceral adipocytes located within the body's central core are maintained at approximately 37°C, adipocytes within bone marrow, subcutaneous, and dermal depots are found primarily within the peripheral shell and generally exist at cooler temperatures. Responses of brown and beige/brite adipocytes to cold stress are well studied; however, comparatively little is known about mechanisms by which white adipocytes adapt to temperatures below 37°C. Here, we report that adaptation of cultured adipocytes to 31°C, the temperature at which distal marrow adipose tissues and subcutaneous adipose tissues often reside, increases anabolic and catabolic lipid metabolism, and elevates oxygen consumption. Cool adipocytes rely less on glucose and more on pyruvate, glutamine, and, especially, fatty acids as energy sources. Exposure of cultured adipocytes and gluteal white adipose tissue (WAT) to cool temperatures activates a shared program of gene expression. Cool temperatures induce stearoyl-CoA desaturase-1 (SCD1) expression and monounsaturated lipid levels in cultured adipocytes and distal bone marrow adipose tissues (BMATs), and SCD1 activity is required for acquisition of maximal oxygen consumption at 31°C.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Temperatura Corporal / Adipócitos Brancos Limite: Animals Idioma: En Revista: PLoS Biol Assunto da revista: BIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regulação da Temperatura Corporal / Adipócitos Brancos Limite: Animals Idioma: En Revista: PLoS Biol Assunto da revista: BIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos