Muscarinic M-3-receptors mediate cholinergic synergism of mitogenesis in airway smooth muscle

Reinout Gosens, Herman Nelemans, M.M Grootte Bromhaar, S McKay, Hans Zaagsma, Herman Meurs

Research output: Contribution to journalArticleAcademicpeer-review

82 Citations (Scopus)

Abstract

Muscarinic receptor agonists have been considered to act synergistically in combination with growth facors on airway smooth muscle growth. Characterization of the proliferative responses and of the receptor subtype(s) involved has not yet been studied. Therefore, we investigated mitogenesis induced by stimulation of muscarinic receptors, alone and in combination with stimulation by platelet-derived growth factor (PDGF). For this purpose, [H-3]thymidine-incorporation was measured at different culture stages in bovine tracheal smooth muscle cells. Functional muscarinic M-3-receptors, as measured by formation of inositol phosphates, were present in unpassaged cells, but were lacking in passage 2 cells. Methacholine (10 PM) by itself was not able to induce a proliferative response in both cell culture stages. However, methacholine interacted synergistically with PDGF in a dose-dependent fashion (0.1-10 muM), but only in cells having functional muscarinic M3-receptors. This synergism could be suppressed significantly by the selective M-3-receptor antagonists DAU 5884 (0.1 muM) and 4-DAMP (10 nM), but not at all by the M-2-subtype selective antagonist gallamine (10 muM). These results show that methacholine potentiates mitogenesis induced by PDGF solely through stimulation of muscarinic M-3-receptors in bovine tracheal smooth muscle cells.

Original languageEnglish
Pages (from-to)257 - 262
Number of pages6
JournalAmerican Journal of Respiratory Cell and Molecular Biology
Volume28
Issue number2
DOIs
Publication statusPublished - Feb-2003

Keywords

  • PROTEIN-COUPLED RECEPTORS
  • SIGNAL-REGULATED KINASE
  • PHOSPHOINOSITIDE METABOLISM
  • MOLECULAR MECHANISMS
  • DNA-SYNTHESIS
  • M2 RECEPTORS
  • BETA-GAMMA
  • ACTIVATION
  • CELLS
  • PROLIFERATION

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