Single cell tracing of Pomc neurons reveals recruitment of 'Ghost' subtypes with atypical identity in a mouse model of obesity.
Stéphane LéonVincent SimonThomas H LeeLukas SteuernagelSamantha ClarkNasim BiglariThierry Lesté-LasserreNathalie DupuyAstrid CannichLuigi BellocchioPhilippe ZizzariCamille AllardDelphine GonzalesYves Le FeuvreEmeline LhuillierAlexandre BrochardJean Charles NicolasJérémie TeillonMacha NikolskiGiovanni MarsicanoXavier FioramontiJens C BrüningDaniela CotaCarmelo QuartaPublished in: Nature communications (2024)
The hypothalamus contains a remarkable diversity of neurons that orchestrate behavioural and metabolic outputs in a highly plastic manner. Neuronal diversity is key to enabling hypothalamic functions and, according to the neuroscience dogma, it is predetermined during embryonic life. Here, by combining lineage tracing of hypothalamic pro-opiomelanocortin (Pomc) neurons with single-cell profiling approaches in adult male mice, we uncovered subpopulations of 'Ghost' neurons endowed with atypical molecular and functional identity. Compared to 'classical' Pomc neurons, Ghost neurons exhibit negligible Pomc expression and are 'invisible' to available neuroanatomical approaches and promoter-based reporter mice for studying Pomc biology. Ghost neuron numbers augment in diet-induced obese mice, independent of neurogenesis or cell death, but weight loss can reverse this shift. Our work challenges the notion of fixed, developmentally programmed neuronal identities in the mature hypothalamus and highlight the ability of specialised neurons to reversibly adapt their functional identity to adult-onset obesogenic stimuli.
Keyphrases
- single cell
- spinal cord
- weight loss
- cell death
- mouse model
- rna seq
- metabolic syndrome
- poor prognosis
- type diabetes
- high throughput
- gene expression
- bariatric surgery
- high fat diet induced
- crispr cas
- young adults
- insulin resistance
- single molecule
- spinal cord injury
- brain injury
- signaling pathway
- binding protein
- subarachnoid hemorrhage
- childhood cancer