Transcriptomics reveals amygdala neuron regulation by fasting and ghrelin thereby promoting feeding

Author:

Peters Christian1ORCID,He Songwei1ORCID,Fermani Federica1ORCID,Lim Hansol1,Ding Wenyu1,Mayer Christian2ORCID,Klein Rüdiger1ORCID

Affiliation:

1. Department of Molecules–Signaling–Development, Max-Planck Institute for Biological Intelligence, 82152 Martinsried, Germany.

2. Laboratory of Neurogenomics, Max-Planck Institute for Biological Intelligence, 82152 Martinsried, Germany.

Abstract

The central amygdala (CeA) consists of numerous genetically defined inhibitory neurons that control defensive and appetitive behaviors including feeding. Transcriptomic signatures of cell types and their links to function remain poorly understood. Using single-nucleus RNA sequencing, we describe nine CeA cell clusters, of which four are mostly associated with appetitive and two with aversive behaviors. To analyze the activation mechanism of appetitive CeA neurons, we characterized serotonin receptor 2a (Htr2a)–expressing neurons (CeA Htr2a ) that comprise three appetitive clusters and were previously shown to promote feeding. In vivo calcium imaging revealed that CeA Htr2a neurons are activated by fasting, the hormone ghrelin, and the presence of food. Moreover, these neurons are required for the orexigenic effects of ghrelin. Appetitive CeA neurons responsive to fasting and ghrelin project to the parabrachial nucleus (PBN) causing inhibition of target PBN neurons. These results illustrate how the transcriptomic diversification of CeA neurons relates to fasting and hormone-regulated feeding behavior.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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