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Leptin-promoted cilia assembly is critical for normal energy balance
Yu Mi Han, … , Bonghee Lee, Min-Seon Kim
Yu Mi Han, … , Bonghee Lee, Min-Seon Kim
Published March 25, 2014
Citation Information: J Clin Invest. 2014;124(5):2193-2197. https://doi.org/10.1172/JCI69395.
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Brief Report Metabolism

Leptin-promoted cilia assembly is critical for normal energy balance

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Abstract

The majority of mammalian cells have nonmotile primary cilia on their surface that act as antenna-like sensory organelles. Genetic defects that result in ciliary dysfunction are associated with obesity in humans and rodents, which suggests that functional cilia are important for controlling energy balance. Here we demonstrated that neuronal cilia lengths were selectively reduced in hypothalami of obese mice with leptin deficiency and leptin resistance. Treatment of N1 hypothalamic neuron cells with leptin stimulated cilia assembly via inhibition of the tumor suppressors PTEN and glycogen synthase kinase 3β (GSK3β). Induction of short cilia in the hypothalamus of adult mice increased food intake and decreased energy expenditure, leading to a positive energy balance. Moreover, mice with short hypothalamic cilia exhibited attenuated anorectic responses to leptin, insulin, and glucose, which indicates that leptin-induced cilia assembly is essential for sensing these satiety signals by hypothalamic neurons. These data suggest that leptin governs the sensitivity of hypothalamic neurons to metabolic signals by controlling the length of the cell’s antenna.

Authors

Yu Mi Han, Gil Myoung Kang, Kyunghee Byun, Hyuk Wan Ko, Joon Kim, Mi-Seon Shin, Hyun-Kyong Kim, So Young Gil, Ji Hee Yu, Bonghee Lee, Min-Seon Kim

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Figure 2

Leptin stimulates cilia assembly in hypothalamic neuron cells.

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Leptin stimulates cilia assembly in hypothalamic neuron cells.
(A) Acety...
(A) Acetylated α-tubulin immunocytochemistry and cilia length measurement in N1 hypothalamic neuron cells treated or not with 100 nM leptin for the indicated times. Scale bars: 25 μm. (B) Changes in cilia length in N1 cells treated with leptin (100 nM for 18 hours) and/or AG490 (1 μM), LY294002 (1 nM), or wortmannin (10 nM), or in cells transfected with control siRNA (si-Control) or Pik3r1 siRNA (si-p85α). (C) Leptin treatment (100 nM for 30 minutes) of N1 cells caused serial phosphorylation of PTEN, AKT, and GSK3β in N1 cells. (D) siRNA-mediated knockdown of PTEN and GSK3β increased cilia length in N1 cells. (E) Effect of leptin treatment (100 nM for 18 hours) on cilia length in N1 cells overexpressing Pten and Gsk3b. (F) Effect of insulin treatment (18 hours) on cilia length in N1 cells. Data are mean ± SEM. *P < 0.05 vs. control; †P < 0.01 vs. leptin alone.

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