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White-to-brown metabolic conversion of human adipocytes by JAK inhibition.
Moisan, Annie; Lee, Youn-Kyoung; Zhang, Jitao David; Hudak, Carolyn S; Meyer, Claas A; Prummer, Michael; Zoffmann, Sannah; Truong, Hoa Hue; Ebeling, Martin; Kiialainen, Anna; Gérard, Régine; Xia, Fang; Schinzel, Robert T; Amrein, Kurt E; Cowan, Chad A.
  • Moisan A; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Lee YK; 1] Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Massachusetts 02138, USA [2] Center for Regenerative Medicine, Massachusetts General Hospital, Boston Massachusetts 02114, USA.
  • Zhang JD; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Hudak CS; 1] Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Massachusetts 02138, USA [2] Center for Regenerative Medicine, Massachusetts General Hospital, Boston Massachusetts 02114, USA.
  • Meyer CA; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Prummer M; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Zoffmann S; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Truong HH; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Ebeling M; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Kiialainen A; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Gérard R; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Xia F; 1] Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Massachusetts 02138, USA [2] Center for Regenerative Medicine, Massachusetts General Hospital, Boston Massachusetts 02114, USA.
  • Schinzel RT; 1] Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Massachusetts 02138, USA [2] Center for Regenerative Medicine, Massachusetts General Hospital, Boston Massachusetts 02114, USA.
  • Amrein KE; Roche Pharma Research and Early Development, Roche Innovation Center Basel, 124 Grenzacherstrasse, Basel CH 4070, Switzerland.
  • Cowan CA; 1] Department of Stem Cell and Regenerative Biology and Harvard Stem Cell Institute, Harvard University, Massachusetts 02138, USA [2] Center for Regenerative Medicine, Massachusetts General Hospital, Boston Massachusetts 02114, USA.
Nat Cell Biol ; 17(1): 57-67, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25487280
ABSTRACT
The rising incidence of obesity and related disorders such as diabetes and heart disease has focused considerable attention on the discovery of new therapeutics. One promising approach has been to increase the number or activity of brown-like adipocytes in white adipose depots, as this has been shown to prevent diet-induced obesity and reduce the incidence and severity of type 2 diabetes. Thus, the conversion of fat-storing cells into metabolically active thermogenic cells has become an appealing therapeutic strategy to combat obesity. Here, we report a screening platform for the identification of small molecules capable of promoting a white-to-brown metabolic conversion in human adipocytes. We identified two inhibitors of Janus kinase (JAK) activity with no precedent in adipose tissue biology that stably confer brown-like metabolic activity to white adipocytes. Importantly, these metabolically converted adipocytes exhibit elevated UCP1 expression and increased mitochondrial activity. We further found that repression of interferon signalling and activation of hedgehog signalling in JAK-inactivated adipocytes contributes to the metabolic conversion observed in these cells. Our findings highlight a previously unknown role for the JAK-STAT pathway in the control of adipocyte function and establish a platform to identify compounds for the treatment of obesity.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Oxazinas / Piperidinas / Piridinas / Pirimidinas / Pirroles / Adipocitos Marrones / Adipocitos Blancos / Janus Quinasa 3 Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Oxazinas / Piperidinas / Piridinas / Pirimidinas / Pirroles / Adipocitos Marrones / Adipocitos Blancos / Janus Quinasa 3 Tipo de estudio: Prognostic_studies Límite: Animals / Humans / Male Idioma: En Año: 2015 Tipo del documento: Article