Journal
EUROPEAN JOURNAL OF IMMUNOLOGY
Volume 46, Issue 8, Pages 1970-1983Publisher
WILEY-BLACKWELL
DOI: 10.1002/eji.201545861
Keywords
EAE; Glucose metabolism; HIF-1 alpha; Leptin; Malnutrition; Th17; Treg cells
Categories
Funding
- NIDDK NIH HHS [R01 DK106090, K08 DK087944] Funding Source: Medline
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Upon activation, T cells require energy for growth, proliferation, and function. Effector T (Teff) cells, such as Th1 and Th17 cells, utilize high levels of glycolytic metabolism to fuel proliferation and function. In contrast, Treg cells require oxidative metabolism to fuel suppressive function. It remains unknown how Teff/Treg-cell metabolism is altered when nutrients are limited and leptin levels are low. We therefore examined the role of malnutrition and associated hypoleptinemia on Teff versus Treg cells. We found that both malnutrition-associated hypoleptinemia and T cell-specific leptin receptor knockout suppressed Teff-cell number, function, and glucose metabolism, but did not alter Treg-cell metabolism or suppressive function. Using the autoimmune mouse model EAE, we confirmed that fasting-induced hypoleptinemia altered Teff-cell, but not Treg-cell, glucose metabolism, and function in vivo, leading to decreased disease severity. To explore potential mechanisms, we examined HIF-1 alpha, a key regulator of Th17 differentiation and Teffcell glucose metabolism, and found HIF-1 alpha expression was decreased in T cell-specific leptin receptor knockout Th17 cells, and in Teff cells from fasted EAE mice, but was unchanged in Treg cells. Altogether, these data demonstrate a selective, cell-intrinsic requirement for leptin to upregulate glucose metabolism and maintain function in Teff, but not Treg cells.
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