Affiliation:
1. Ecole normale supérieure, Département de Biologie, 75005 Paris, France
2. CNRS UMR8542, 75005 Paris, France
3. CNRS-FRE3093, Université de Nice-Sophia Antipolis, 06108 Nice, France
Abstract
In the last few years, elucidation of the architecture of breathing control centres has reached the cellular level. This has been facilitated by increasing knowledge of the molecular signatures of various classes of hindbrain neurons. Here, we review the advances achieved by studying the homeodomain factorPhox2b, a transcriptional determinant of neuronal identity in the central and peripheral nervous systems. Evidence from human genetics, neurophysiology and mouse reverse genetics converges to implicate a small population ofPhox2b-dependent neurons, located in the retrotrapezoid nucleus, in the detection of CO2, which is a paramount source of the ‘drive to breathe’. Moreover, the same and other studies suggest that an overlapping or identical neuronal population, the parafacial respiratory group, might contribute to the respiratory rhythm at least in some circumstances, such as for the initiation of breathing following birth. Together with the previously establishedPhox2bdependency of other respiratory neurons (which we review briefly here), our new data highlight a key role of this transcription factor in setting up the circuits for breathing automaticity.
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Cited by
45 articles.
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