A(2B) adenosine receptors increase cytokine release by bronchial smooth muscle cells

Am J Respir Cell Mol Biol. 2004 Jan;30(1):118-25. doi: 10.1165/rcmb.2003-0118OC. Epub 2003 Jul 10.


Adenosine (Ado) has been suggested to play a role in inflammatory airway diseases such as asthma and chronic obstructive pulmonary disease. The goal of this study was to determine the effect of Ado and its receptor subtypes on cytokine release by bronchial smooth muscle cells. The A2B Ado receptor (AdoR) was expressed at the highest level among the four AdoR subtypes. Activation of the A2B AdoR by an Ado analog, 5'-(N-ethylcarboxamido)-adenosine (NECA), increased cAMP accumulation with potency (EC50 value) of 21.2 +/- 0.2 microM. The effect of NECA on the expression of the inflammatory cytokines was determined using a cDNA array consisting of 23 cytokine genes and confirmed using real-time reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay. NECA increased the release of interleukin-6 and monocyte chemotactic protein-1 proteins with EC50 values of 1.26 +/- 0.25 microM and 0.40 +/- 0.08 microM, respectively, and the maximal folds of induction were 20.8 +/- 1.7- and 6.4 +/- 0.7-fold, respectively. Selective agonists for the A1, A2A, and A3 AdoR subtypes had no effect on cytokine release. The effects of NECA were attenuated by selective antagonists of the A2B AdoR. Thus, Ado increases the release of interleukin-6 and monocyte chemotactic protein-1 from bronchial smooth muscle cells via activation of the A2B AdoR. Our findings provide a novel mechanism whereby Ado acts as a proinflammatory mediator in the airway.

MeSH terms

  • Adenosine A2 Receptor Antagonists
  • Base Sequence
  • Bronchi / cytology
  • Bronchi / metabolism*
  • Cells, Cultured
  • Cytokines / metabolism*
  • DNA Primers
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Muscle, Smooth / cytology
  • Muscle, Smooth / metabolism*
  • RNA, Messenger / genetics
  • Receptor, Adenosine A2B / genetics
  • Receptor, Adenosine A2B / physiology*


  • Adenosine A2 Receptor Antagonists
  • Cytokines
  • DNA Primers
  • RNA, Messenger
  • Receptor, Adenosine A2B