eLifeNeurosciencePeer-reviewed journal article
Knockdown of PHOX2B in the retrotrapezoid nucleus reduces the central CO2 chemoreflex in rats
Silvia CardaniiD, Tara Adele JanesiD, William BetzneriD, Silvia PagliardiniiD
Abstract
PHOX2B is a transcription factor essential for the development of different classes of neurons in the central and peripheral nervous system. Heterozygous mutations in the PHOX2B coding region are responsible for the occurrence of Congenital Central Hypoventilation Syndrome (CCHS), a rare neurological disorder characterised by inadequate chemosensitivity and life-threatening sleep- related hypoventilation. Animal studies suggest that chemoreflex defects are caused in part by the improper development or function of PHOX2B expressing neurons in the retrotrapezoid nucleus (RTN), a central hub for CO2 chemosensitivity. Although the function of PHOX2B in rodents during development is well established, its role in the adult respiratory network remains unknown. In this study, we investigated whether reduction in PHOX2B expression in chemosensitive neuromedin-B (NMB) expressing neurons in the RTN altered respiratory function. Four weeks following local RTN injection of a lentiviral vector expressing the short hairpin RNA (shRNA) targeting Phox2b mRNA, a reduction of PHOX2B expression was observed in Nmb neurons compared to both naive rats and rats injected with the non-target shRNA. PHOX2B knockdown did not affect breathing in room air or under hypoxia, but ventilation was significantly impaired during hypercapnia. PHOX2B knockdown did not alter Nmb expression but it was associated with reduced the expression of both Task2 and Gpr4, two CO2 sensors in the RTN. We conclude that PHOX2B in the adult brain has an important role in CO2 chemoreception and reduced PHOX2B expression in CCHS beyond the developmental period may contribute to the impaired central chemoreflex function.
- Citations
- 7
- FWCI
- 1.51
- Field percentile
- top 21%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia
Caroline B. Ferreira, Talita M. Silva, … Thiago Santos Moreira·eLifePeer-reviewed·Nov 17, 2022
- Genetic identification of novel medullary neurons underlying congenital central hypoventilation syndrome
Ke Cui, Yiling Xia, … Luis Rodrigo Hernandez-Miranda·bioRxiv·May 29, 2023
- Serotonin, Etonogestrel and breathing activity in murine Congenital Central Hypoventilation Syndrome
A. Casciato, L. Bianchi, … L. Bodineau·bioRxiv·Apr 19, 2022
- OBSTRUCTIVE APNEAS IN A MOUSE MODEL OF CONGENITAL CENTRAL HYPOVENTILATION SYNDROME
A. Madani, G. Pitollat, … B. Matrot·bioRxiv·Feb 15, 2021
- Vascular control of the CO2/H+ dependent drive to breathe
Colin M. Cleary, Thiago Santos Moreira, … Daniel Kent Mulkey·eLifePeer-reviewed·Sep 14, 2020
- Analyzing the neuroglial brainstem circuits for respiratory chemosensitivity in freely moving mice
Amol Bhandare, Joseph van de Wiel, … Nicholas Dale·eLifePeer-reviewed·Oct 25, 2022