Author
Listed:
- Jonathan R. Brestoff
(Jill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University
Perelman School of Medicine, University of Pennsylvania)
- Brian S. Kim
(Perelman School of Medicine, University of Pennsylvania
Present addresses: Division of Dermatology, Department of Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA (B.S.K.); Immunology Research, Biogen Idec, Inc., Cambridge, Massachusetts 02142, USA (S.A.S.).)
- Steven A. Saenz
(Perelman School of Medicine, University of Pennsylvania
Present addresses: Division of Dermatology, Department of Medicine, Washington University School of Medicine, St Louis, Missouri 63110, USA (B.S.K.); Immunology Research, Biogen Idec, Inc., Cambridge, Massachusetts 02142, USA (S.A.S.).)
- Rachel R. Stine
(Institute for Diabetes, Obesity and Metabolism, Perelman School of Medicine, University of Pennsylvania)
- Laurel A. Monticelli
(Jill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University
Perelman School of Medicine, University of Pennsylvania)
- Gregory F. Sonnenberg
(Jill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University)
- Joseph J. Thome
(Columbia Center for Translational Immunology, Columbia University Medical Center
Columbia University Medical Center)
- Donna L. Farber
(Columbia Center for Translational Immunology, Columbia University Medical Center
Columbia University Medical Center
Columbia University Medical Center)
- Kabirullah Lutfy
(College of Pharmacy, Western University of Health Sciences)
- Patrick Seale
(Institute for Diabetes, Obesity and Metabolism, Perelman School of Medicine, University of Pennsylvania)
- David Artis
(Jill Roberts Institute for Research in IBD, Weill Cornell Medical College, Cornell University
Perelman School of Medicine, University of Pennsylvania)
Abstract
Group 2 innate lymphoid cells are shown to have a critical role in energy homeostasis by producing methionine-enkephalin peptides in response to interleukin 33, thus promoting the beiging of white adipose tissue; increased numbers of beige (also known as brown-like or brite) fat cells in white adipose tissue leads to increased energy expenditure and decreased adiposity.
Suggested Citation
Jonathan R. Brestoff & Brian S. Kim & Steven A. Saenz & Rachel R. Stine & Laurel A. Monticelli & Gregory F. Sonnenberg & Joseph J. Thome & Donna L. Farber & Kabirullah Lutfy & Patrick Seale & David Ar, 2015.
"Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity,"
Nature, Nature, vol. 519(7542), pages 242-246, March.
Handle:
RePEc:nat:nature:v:519:y:2015:i:7542:d:10.1038_nature14115
DOI: 10.1038/nature14115
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