Cao Haiming, Gerhold Kristin, Mayers Jared R, Wiest Michelle M, Watkins Steven M, Hotamisligil Gökhan S
Department of Genetics and Complex Diseases, Harvard School of Public Health, Boston, MA 02115, USA.
Cell. 2008 Sep 19;134(6):933-44. doi: 10.1016/j.cell.2008.07.048.
Dysregulation of lipid metabolism in individual tissues leads to systemic disruption of insulin action and glucose metabolism. Utilizing quantitative lipidomic analyses and mice deficient in adipose tissue lipid chaperones aP2 and mal1, we explored how metabolic alterations in adipose tissue are linked to whole-body metabolism through lipid signals. A robust increase in de novo lipogenesis rendered the adipose tissue of these mice resistant to the deleterious effects of dietary lipid exposure. Systemic lipid profiling also led to identification of C16:1n7-palmitoleate as an adipose tissue-derived lipid hormone that strongly stimulates muscle insulin action and suppresses hepatosteatosis. Our data reveal a lipid-mediated endocrine network and demonstrate that adipose tissue uses lipokines such as C16:1n7-palmitoleate to communicate with distant organs and regulate systemic metabolic homeostasis.
个体组织中脂质代谢的失调会导致胰岛素作用和葡萄糖代谢的全身性紊乱。利用定量脂质组学分析以及缺乏脂肪组织脂质伴侣蛋白aP2和mal1的小鼠,我们探究了脂肪组织中的代谢改变如何通过脂质信号与全身代谢相联系。从头脂肪生成的显著增加使这些小鼠的脂肪组织对饮食脂质暴露的有害影响产生抗性。全身性脂质分析还导致鉴定出C16:1n7-棕榈油酸酯是一种源自脂肪组织的脂质激素,它能强烈刺激肌肉胰岛素作用并抑制肝脂肪变性。我们的数据揭示了一个脂质介导的内分泌网络,并证明脂肪组织利用诸如C16:1n7-棕榈油酸酯之类的脂肪因子与远处器官进行通信并调节全身代谢稳态。