Genetic ablation of lymphocytes and cytokine signaling in nonobese diabetic mice prevents diet‐induced obesity and insulin resistance. Issue 3 (7th December 2015)
- Record Type:
- Journal Article
- Title:
- Genetic ablation of lymphocytes and cytokine signaling in nonobese diabetic mice prevents diet‐induced obesity and insulin resistance. Issue 3 (7th December 2015)
- Main Title:
- Genetic ablation of lymphocytes and cytokine signaling in nonobese diabetic mice prevents diet‐induced obesity and insulin resistance
- Authors:
- Friedline, Randall H.
Ko, Hwi Jin
Jung, Dae Young
Lee, Yongjin
Bortell, Rita
Dagdeviren, Sezin
Patel, Payal R.
Hu, Xiaodi
Inashima, Kunikazu
Kearns, Caitlyn
Tsitsilianos, Nicholas
Shafiq, Umber
Shultz, Leonard D.
Lee, Ki Won
Greiner, Dale L.
Kim, Jason K. - Abstract:
- Abstract : Obesity is characterized by a dysregulated immune system, which may causally associate with insulin resistance and type 2 diabetes. Despite widespread use of nonobese diabetic (NOD) mice, NOD with severe combined immunodeficiency ( scid ) mutation (SCID) mice, and SCID bearing a null mutation in the IL‐2 common g chain receptor (NSG) mice as animal models of human diseases including type 1 diabetes, the underlying metabolic effects of a genetically altered immune system are poorly understood. For this, we performed a comprehensive metabolic characterization of these mice fed chow or after 6 wk of a high‐fat diet. We found that NOD mice had ~50% less fat mass and were 2‐fold more insulin sensitive, as measured by hyperinsulinemic‐euglycemic clamp, than C57BL/6 wild‐type mice. SCID mice were also more insulin sensitive with increased muscle glucose metabolism and resistant to diet‐induced obesity due to increased energy expenditure (~10%) and physical activity (~40%) as measured by metabolic cages. NSG mice were completely protected from diet‐induced obesity and insulin resistance with significant increases in glucose metabolism in peripheral organs. Our findings demonstrate an important role of genetic background, lymphocytes, and cytokine signaling in diet‐induced obesity and insulin resistance.—Friedline, R. H., Ko, H.J., Jung, D. Y., Lee, Y., Bortell, R., Dagdeviren, S., Patel, P. R., Hu, X., Inashima, K., Kearns, C., Tsitsilianos, N., Shafiq, U., Shultz, L. D.,Abstract : Obesity is characterized by a dysregulated immune system, which may causally associate with insulin resistance and type 2 diabetes. Despite widespread use of nonobese diabetic (NOD) mice, NOD with severe combined immunodeficiency ( scid ) mutation (SCID) mice, and SCID bearing a null mutation in the IL‐2 common g chain receptor (NSG) mice as animal models of human diseases including type 1 diabetes, the underlying metabolic effects of a genetically altered immune system are poorly understood. For this, we performed a comprehensive metabolic characterization of these mice fed chow or after 6 wk of a high‐fat diet. We found that NOD mice had ~50% less fat mass and were 2‐fold more insulin sensitive, as measured by hyperinsulinemic‐euglycemic clamp, than C57BL/6 wild‐type mice. SCID mice were also more insulin sensitive with increased muscle glucose metabolism and resistant to diet‐induced obesity due to increased energy expenditure (~10%) and physical activity (~40%) as measured by metabolic cages. NSG mice were completely protected from diet‐induced obesity and insulin resistance with significant increases in glucose metabolism in peripheral organs. Our findings demonstrate an important role of genetic background, lymphocytes, and cytokine signaling in diet‐induced obesity and insulin resistance.—Friedline, R. H., Ko, H.J., Jung, D. Y., Lee, Y., Bortell, R., Dagdeviren, S., Patel, P. R., Hu, X., Inashima, K., Kearns, C., Tsitsilianos, N., Shafiq, U., Shultz, L. D., Lee, K. W., Greiner, D. L., Kim, J. K., Genetic ablation of lymphocytes and cytokine signaling in nonobese diabetic mice prevents diet‐induced obesity and insulin resistance. FASEB J. 30, 1328–1338 (2016). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 30:Issue 3(2016)
- Journal:
- FASEB journal
- Issue:
- Volume 30:Issue 3(2016)
- Issue Display:
- Volume 30, Issue 3 (2016)
- Year:
- 2016
- Volume:
- 30
- Issue:
- 3
- Issue Sort Value:
- 2016-0030-0003-0000
- Page Start:
- 1328
- Page End:
- 1338
- Publication Date:
- 2015-12-07
- Subjects:
- glucose metabolism -- energy balance -- diabetes mouse models
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.15-280610 ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13314.xml