Differential expression of connexin26 and connexin32 in the pre-Bötzinger complex of neonatal and adult rat

Ann Shyn Chiang, Yee Chien Liu, Shu Ling Chiu, Shu Hsia Hu, Chih Ying Huang, Chang Huain Hsieh

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

The pre-Bötzinger complex (pre-BötC) is hypothesized to be the site for respiratory rhythm generation in mammals. Studies examining the cellular mechanisms mediating rhythm generation have focused on the role of chemically mediated synaptic interactions; however, electrotonic synaptic interactions (i.e., electrotonic coupling), which occur by means of gap junctions, may also play a role. Here, we used immunoblot and immunohistochemical analyses to determine whether the pre-BötC contains the gap junction proteins necessary for electrotonic communication and whether the presence and distribution of these gap junction proteins show a developmental change in expression. We found that both connexin26 (Cx26) and connexin32 (Cx32) were expressed in pre-BötC neurons of neonatal and adult rats; however, the relative amounts and their distribution varied by age. Cx26 labeling was seen in a high proportion of pre-BötC neurons in neonatal rats ≤ 7 days postnatal (P7) but declined with increasing age. In contrast, Cx32 labeling was sparse in pre-BötC neurons of neonatal rats ≤ P7, but increased with increasing age; the highest proportion was seen in adult rats. These data suggest the potential for gap junctional communication in the pre-BötC of both neonatal and adult rats, and we propose that the gap junction proteins Cx26 and Cx32 form the neuroanatomic substrate for this gap junctional communication, which may be important in the synchronization of neural activity generating respiratory rhythm.

Original languageEnglish (US)
Pages (from-to)12-19
Number of pages8
JournalJournal of Comparative Neurology
Volume440
Issue number1
DOIs
StatePublished - Nov 5 2001
Externally publishedYes

Keywords

  • Connexin
  • Control of breathing
  • Development
  • Gap junctions
  • Immunoblot
  • Immunohistochemistry
  • Respiratory rhythmogenesis

ASJC Scopus subject areas

  • Neuroscience(all)

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