Molecular and functional identification of β-adrenergic receptors in distal convoluted tubule cells

Frank A. Gesek, Kenneth E. White

Research output: Contribution to journalArticlepeer-review

5 Scopus citations


Renal nerve stimulation or circulating catecholamines activate the β-adrenergic receptors that mediate direct effects on tubular transport. Three subtypes of β-adrenergic receptors have been characterized: βi, β2, and βs. β-Adrenergic-receptor effects on Na+ and Ca2+ transport in distal convoluted tubules (DOT) have not been established. The focus of this study was to 1 ) identify the subtypes of β-adrenergic receptors in DCT cells and 2) examine functional responses to β-receptor activation on adenosine 3', 5'cyclic monophosphate (cAMP) formation and Na+ and Ca2+ entry. To determine the subtypes of β-receptors present, RNA isolated from immortalized mouse DCT cells was reverse transcribed, and the cDNA was amplified using primers designed to reported sequences for βj-, β2-, and β3-receptor subtypes. Products of the appropriate sizes were obtained with βi- and β2-primers. No product was observed with primers to the 3 sequence. Receptor products were confirmed by sequencing and are identical to reported mouse βi- and βa-receptor sequence. Receptor binding of [3H]dihydroalprenolol was 123 ±13 fmol/mg protein, and a 3:1 ratio of βr to β2-receptors was observed with DCT cell membranes. Isoproterenol, a β-receptor agonist, increased cAMP formation 8.5-fold. Pretreatment with the antagonist propranolol abolished agonist-induced cAMP accumulation. Isoproterenol significantly increased 22Na+ uptake to 345 ±23 compared with a basal rate of 256 ±12 nmol min ~! mg protein ~' and was blocked with propranolol and βr and β2-selective antagonists. Isoproterenol had no effect on 45Ca2+ entry into DCT cells. In summary, DCT cells express three times more βr than β2-receptors and express no detectable βs-adrenergic receptors. β-Receptors couple to adenylyl cyclase, and activation of β-adrenergic receptors increases Na+ but not Ca2+ entry in DCT cells.

Original languageEnglish (US)
Pages (from-to)F721-F728
JournalAmerican Journal of Physiology
Issue number6 PART 2
StatePublished - Dec 1 1997
Externally publishedYes


  • Adenylyl cyclase
  • Adrenergic receptor
  • Calcium transport
  • Distal convoluted tubule
  • Isoproterenol
  • Propranolol
  • Sodium transport

ASJC Scopus subject areas

  • Physiology (medical)

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