RET proto-oncogene is important for the development of respiratory CO2 sensitivity

  • Melvin D. Burton
  • , Akira Kawashima
  • , James A. Brayer
  • , Homayoun Kazemi
  • , Daniel C. Shannon
  • , Anita Schuchardt
  • , Frank Costantini
  • , Vassilis Pachnis
  • , T. Bernard Kinane

Research output: Contribution to journalArticlepeer-review

97 Scopus citations

Abstract

Brain stem muscarinic cholinergic pathways are important in respiratory carbon dioxide (GO,) chemosensitivity. Defects in the muscarinic system have been reported in children with congenital/developmental disorders of respiratory control such as sudden infant death syndrome (SIDS) and congenital central hypoventilation syndrome (CCHS). This early onset of disease suggests a possible genetic basis. The muscarinic system is part of the autonomic nervous system which develops from the neural crest. Ret proto-oncogene is important for this development. Thus, a potential role for ret in the development of respiratory CO2 chemosensitivity was considered. Using plethysmography, we assessed the ventilatory response to inhaled CO2 in the unanesthetized offsprings of ret(+/-) mice. Fractional increases in minute ventilation during hypercapnia relative to isocapnia were 5.1 ± 3.2, 3.0 ± 1.6 and 1.4 ± 0.8 for the ret(+/+), ret(+/-) and ret(-/-) mice, respectively. The ret knockout mice have a depressed ventilatory response to inhaled CO2. Therefore, the ret gene is an important factor in the pathway of neuronal development which allow respiratory CO2 chemosensitivity.

Original languageEnglish (US)
Pages (from-to)137-143
Number of pages7
JournalJournal of the Autonomic Nervous System
Volume63
Issue number3
DOIs
StatePublished - Apr 14 1997
Externally publishedYes

Bibliographical note

Funding Information:
This work was supported by the NIDDK DK 02271-03, the Hearst Fund and the Shoolman Fund of the MGH Pulmonary and Critical Care Unit.

Keywords

  • Control of respiration
  • Genetics
  • Knockout mouse
  • Respiratory chemosensitivity
  • Ret proto-oncogene

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