Clusterin/ApoJ enhances central leptin signaling through Lrp2‐mediated endocytosis
Clusterin/ApoJ enhances central leptin signaling through Lrp2‐mediated endocytosis
Hypothalamic leptin signaling plays a central role in maintaining body weight homeostasis. Here, we show that clusterin/ApoJ, recently identified as an anorexigenic neuropeptide, is an important regulator in the hypothalamic leptin signaling pathway. Coadministration of clusterin potentiates the anorexigenic effect of leptin and boosts leptin-induced hypothalamic Stat3 activation. In cultured neurons, clusterin enhances receptor binding and subsequent endocytosis of leptin. These effects are mainly mediated through the LDL receptor-related protein-2 (Lrp2). Notably, inhibition of hypothalamic clusterin, Lrp2 or endocytosis abrogates anorexia and hypothalamic Stat3 activation caused by leptin. These findings propose a novel regulatory mechanism in central leptin signaling pathways.
- University of Ulsan Korea (Republic of)
- Asan Medical Center Korea (Republic of)
- Beth Israel Deaconess Medical Center United States
- Gachon University Korea (Republic of)
- Incheon National University Korea (Republic of)
Leptin, Male, Mice, Knockout, Neurons, Hypothalamus, Endocytosis, Low Density Lipoprotein Receptor-Related Protein-2, Mice, Clusterin, Animals, Receptors, Leptin, Protein Binding, Signal Transduction
Leptin, Male, Mice, Knockout, Neurons, Hypothalamus, Endocytosis, Low Density Lipoprotein Receptor-Related Protein-2, Mice, Clusterin, Animals, Receptors, Leptin, Protein Binding, Signal Transduction
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