An organism-wide atlas of hormonal signaling based on the mouse lemur single-cell transcriptome.
Shixuan LiuCamille EzranMichael F Z WangZhengda LiKyle Awayannull nullJonathan Z LongIwijn De VlaminckSheng WangJacques EpelbaumChristin S KuoJérémy TerrienMark A KrasnowJames E FerrellPublished in: Nature communications (2024)
Hormones mediate long-range cell communication and play vital roles in physiology, metabolism, and health. Traditionally, endocrinologists have focused on one hormone or organ system at a time. Yet, hormone signaling by its very nature connects cells of different organs and involves crosstalk of different hormones. Here, we leverage the organism-wide single cell transcriptional atlas of a non-human primate, the mouse lemur (Microcebus murinus), to systematically map source and target cells for 84 classes of hormones. This work uncovers previously-uncharacterized sites of hormone regulation, and shows that the hormonal signaling network is densely connected, decentralized, and rich in feedback loops. Evolutionary comparisons of hormonal genes and their expression patterns show that mouse lemur better models human hormonal signaling than mouse, at both the genomic and transcriptomic levels, and reveal primate-specific rewiring of hormone-producing/target cells. This work complements the scale and resolution of classical endocrine studies and sheds light on primate hormone regulation.
Keyphrases
- single cell
- rna seq
- induced apoptosis
- cell cycle arrest
- high throughput
- genome wide
- endothelial cells
- healthcare
- public health
- polycystic ovary syndrome
- mental health
- type diabetes
- oxidative stress
- cell death
- signaling pathway
- poor prognosis
- stem cells
- induced pluripotent stem cells
- mesenchymal stem cells
- dna methylation
- transcription factor
- risk assessment
- long non coding rna
- cell proliferation
- skeletal muscle