| Literature DB >> 35614045 |
Polina Kameneva1,2, Victoria I Melnikova3, Maria Eleni Kastriti1,2, Anastasia Kurtova3, Emil Kryukov1,2, Aliia Murtazina2, Louis Faure1, Irina Poverennaya1, Artem V Artemov1,4, Tatiana S Kalinina5, Nikita V Kudryashov5,6, Michael Bader7,8,9,10, Jan Skoda11,12, Petr Chlapek11,12, Lucie Curylova11,12, Lukas Sourada11,12, Jakub Neradil11,12, Marketa Tesarova13, Massimo Pasqualetti14,15, Patricia Gaspar16, Vasily D Yakushov17, Boris I Sheftel17, Tomas Zikmund13, Jozef Kaiser13, Kaj Fried18, Natalia Alenina7,8, Elena E Voronezhskaya19, Igor Adameyko20,21.
Abstract
Adrenal glands are the major organs releasing catecholamines and regulating our stress response. The mechanisms balancing generation of adrenergic chromaffin cells and protecting against neuroblastoma tumors are still enigmatic. Here we revealed that serotonin (5HT) controls the numbers of chromaffin cells by acting upon their immediate progenitor "bridge" cells via 5-hydroxytryptamine receptor 3A (HTR3A), and the aggressive HTR3Ahigh human neuroblastoma cell lines reduce proliferation in response to HTR3A-specific agonists. In embryos (in vivo), the physiological increase of 5HT caused a prolongation of the cell cycle in "bridge" progenitors leading to a smaller chromaffin population and changing the balance of hormones and behavioral patterns in adulthood. These behavioral effects and smaller adrenals were mirrored in the progeny of pregnant female mice subjected to experimental stress, suggesting a maternal-fetal link that controls developmental adaptations. Finally, these results corresponded to a size-distribution of adrenals found in wild rodents with different coping strategies.Entities:
Mesh:
Substances:
Year: 2022 PMID: 35614045 PMCID: PMC9133002 DOI: 10.1038/s41467-022-30438-w
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 17.694