CaMK1D signalling in AgRP neurons promotes ghrelin-mediated food intake

Hypothalamic AgRP/NPY neurons are key players in the control of feeding behaviour. Ghrelin, a major orexigenic hormone, activates AgRP/NPY neurons to stimulate food intake and adiposity. However, cell-autonomous ghrelin-dependent signalling mechanisms in AgRP/NPY neurons remain poorly defined. Here we show that calcium/calmodulin-dependent protein kinase ID (CaMK1D), a genetic hot spot in type 2 diabetes, is activated upon ghrelin stimulation and acts in AgRP/NPY neurons to mediate ghrelin-dependent food intake. Global Camk1d-knockout male mice are resistant to ghrelin, gain less body weight and are protected against high-fat-diet-induced obesity. Deletion of Camk1d in AgRP/NPY, but not in POMC, neurons is sufficient to recapitulate above phenotypes. In response to ghrelin, lack of CaMK1D attenuates phosphorylation of CREB and CREB-dependent expression of the orexigenic neuropeptides AgRP/NPY in fibre projections to the paraventricular nucleus (PVN). Hence, CaMK1D links ghrelin action to transcriptional control of orexigenic neuropeptide availability in AgRP neurons. The authors show that the protein kinase CaMK1D acts on AgRP/NPY neurons to promote ghrelin's effects in mediating food intake in male mice.

Automated summary

The protein kinase CaMK1D acts on AgRP/NPY neurons to promote ghrelin's effects in mediating food intake in male mice. Ghrelin stimulation activates CaMK1D and its lack reduces the response to ghrelin, leading to decreased body weight gain and protection against high-fat-diet-induced obesity. CaMK1D links ghrelin action to transcriptional control of orexigenic neuropeptide availability in AgRP neurons.