Macrophage-specific de Novo synthesis of ceramide is dispensable for inflammasome-driven inflammation and insulin resistance in obesity

Christina D. Camell, Kim Y. Nguyen, Michael J. Jurczak, Brooke E. Christian, Gerald I. Shulman, Gerald S. Shadel, Vishwa Deep Dixit

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Dietary lipid overload and calorie excess during obesity is a low grade chronic inflammatory state with diminished ability to appropriately metabolize glucose or lipids. Macrophages are critical in maintaining adipose tissue homeostasis, in part by regulating lipid metabolism, energy homeostasis, and tissue remodeling. During high fat diet-induced obesity, macrophages are activated by lipid derived "danger signals" such as ceramides and palmitate and promote the adipose tissue inflammation in an Nlrp3 inflammasome-dependent manner. Given that the metabolic fate of fatty acids in macrophages is not entirely elucidated, we have hypothesized that de novo synthesis of ceramide, through the rate-limiting enzyme serine palmitoyltransferase long chain (Sptlc)-2, is required for saturated fatty aciddriven Nlrp3 inflammasome activation in macrophages. Here we report that mitochondrial targeted overexpression of catalase, which is established to mitigate oxidative stress, controls ceramide-induced Nlrp3 inflammasome activation but does not affect the ATP-mediated caspase-1 cleavage. Surprisingly, myeloid cell-specific deletion of Sptlc2 is not required for palmitatedriven Nlrp3 inflammasome activation. Furthermore, the ablation of Sptlc2 in macrophages did not impact macrophage polarization or obesity-induced adipose tissue leukocytosis. Consistent with these data, investigation of insulin resistance using hyperinsulinemic-euglycemic clamps revealed no significant differences in obese mice lacking ceramide de novo synthesis machinery in macrophages. These data suggest that alternate metabolic pathways control fatty acid-derived ceramide synthesis in macrophage and the Nlrp3 inflammasome activation in obesity.

Original languageEnglish (US)
Pages (from-to)29402-29413
Number of pages12
JournalJournal of Biological Chemistry
Volume290
Issue number49
DOIs
StatePublished - Dec 4 2015

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Inflammasomes
Macrophages
Ceramides
Insulin Resistance
Obesity
Insulin
Inflammation
Chemical activation
Adipose Tissue
Lipids
Tissue
Serine C-Palmitoyltransferase
Homeostasis
Fatty Acids
Tissue homeostasis
Obese Mice
Caspase 1
Glucose Clamp Technique
Macrophage Activation
Palmitates

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Macrophage-specific de Novo synthesis of ceramide is dispensable for inflammasome-driven inflammation and insulin resistance in obesity. / Camell, Christina D.; Nguyen, Kim Y.; Jurczak, Michael J.; Christian, Brooke E.; Shulman, Gerald I.; Shadel, Gerald S.; Dixit, Vishwa Deep.

In: Journal of Biological Chemistry, Vol. 290, No. 49, 04.12.2015, p. 29402-29413.

Research output: Contribution to journalArticle

Camell, Christina D. ; Nguyen, Kim Y. ; Jurczak, Michael J. ; Christian, Brooke E. ; Shulman, Gerald I. ; Shadel, Gerald S. ; Dixit, Vishwa Deep. / Macrophage-specific de Novo synthesis of ceramide is dispensable for inflammasome-driven inflammation and insulin resistance in obesity. In: Journal of Biological Chemistry. 2015 ; Vol. 290, No. 49. pp. 29402-29413.
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