Abstract

Secretory phospholipase A2 group IIA (PLA2G2A) is a member of a family of secretory phospholipases that have been implicated in inflammation, atherogenesis, and antibacterial actions. Here, we evaluated the role of PLA2G2A in the metabolic response to a high fat diet. C57BL/6 (BL/6) mice do not express PLA2g2a due to a frameshift mutation. We fed BL/6 mice expressing the human PLA2G2A gene (IIA+ mice) a fat diet and assessed the physiologic response. After 10 weeks on the high fat diet, the BL/6 mice were obese, but the IIA+ mice did not gain weight or accumulate lipid. The lean mass in chow- and high fat-fed IIA+ mice was constant and similar to the BL/6 mice on a chow diet. Surprisingly, the IIA+ mice had an elevated metabolic rate, which was not due to differences in physical activity. The IIA+ mice were more insulin sensitive and glucose tolerant than the BL/6 mice, even when the IIA+ mice were provided the high fat diet. The IIA+ mice had increased expression of uncoupling protein 1 (UCP1), sirtuin 1 (SIRT1), and PPARγ coactivator 1α (PGC-1α) in brown adipose tissue (BAT), suggesting that PLA2G2A activates mitochondrial uncoupling in BAT. Our data indicate that PLA2G2A has a previously undiscovered impact on insulin sensitivity and metabolism.

Highlights

  • Secretory phospholipase A2 group IIA (PLA2G2A) is a member of a family of secretory phospholipases that have been implicated in inflammation, atherogenesis, and antibacterial actions

  • Effect of secretory phospholipase A2 group IIA (PLA2G2A) on weight gain Initially, we evaluated the effect of PLA2G2A on weight gain and lipid accumulation by monitoring the body composition in response to 10 weeks of high fat diet consumption in both BL/6 control and the IIA+ mice [15]

  • BL/6 mice receiving the high fat diet had significantly elevated total body fat compared with their chow counterparts, whereas fat mass was slightly lower in the IIA+ groups regardless of the diet (Fig. 1C)

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Summary

Introduction

Secretory phospholipase A2 group IIA (PLA2G2A) is a member of a family of secretory phospholipases that have been implicated in inflammation, atherogenesis, and antibacterial actions. SPLA2 group IIA (PLA2G2A) was first purified from the platelets and synovial fluids of patients suffering from arthritis [6]. It has high affinity for anionic phospholipids such as phosphatidylserine, phosphatidylethanolamine, and phosphatidylglycerol [5]. The finding that PLA2G2A is highly abundant in biological fluids of patients suffering from inflammatory diseases, like arthritis, sepsis, and myocardial infarctions, suggested that PLA2G2A promotes inflammation [5, 13, 14] In support of this concept, under inflammatory conditions PLA2g2a knockout BALB/c mice have attenuated joint inflammation compared with wild-type BALB/c mice [15].

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