Serotonin metabolism in rat mesangial cells: involvement of a serotonin transporter and monoamine oxidase A

Kidney Int. 1999 Oct;56(4):1391-9. doi: 10.1046/j.1523-1755.1999.00673.x.

Abstract

Background: Serotonin is one of the factors regulating mesangial cell proliferation, and convergent evidence supports its involvement in the development of glomerulonephritis. In this study, we identified a serotonin transporter and the amine-degrading enzyme monoamine oxidases (MAOs) in mesangial cells, and we studied their involvement in serotonin degradation.

Methods: MAOs were characterized in membrane preparations and intact mesangial cells by enzyme assay using [14C]5-hydroxytryptamine and [14C]beta-phenylethylamine as specific substrates for MAO-A and MAO-B, respectively, and by Western blot analysis. The expression of a serotonin transporter was determined by [14C]5-hydroxytryptamine uptake experiments and Western blot. Mesangial cell proliferation was measured by BrdU incorporation.

Results: Quantitation of the MAO isoforms by enzyme assay and Western blot analysis showed that MAO-A was largely predominant in mesangial cells, accounting for approximately 90% of the total enzyme population. The MAO substrate [14C]serotonin was transported into mesangial cells by a saturable uptake system (Vmax 310 +/- 36 pmol/30 min/mg protein; Km 5.9 +/- 1.4 microM) displaying the pharmacological properties of a serotonin transporter. The expression of a serotonin transporter was confirmed by Western blot analysis. MAO activity measured in intact cells showed that after accumulation into mesangial cells, [14C]serotonin was metabolized by MAO-A. Finally, serotonin-mediated mesangial cell proliferation was significantly increased after irreversible MAO inhibition.

Conclusions: Our results suggest that serotonin concentration and function in glomeruli may be regulated in part by its transport into mesangial cells and degradation by MAO-A.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antimetabolites / metabolism
  • Antimetabolites / pharmacology
  • Biological Transport / physiology
  • Blotting, Western
  • Bromodeoxyuridine / metabolism
  • Bromodeoxyuridine / pharmacology
  • Carbon Radioisotopes
  • Carrier Proteins / metabolism*
  • Cell Division / physiology
  • Cells, Cultured
  • Enzyme Activation / physiology
  • Glomerular Mesangium / chemistry*
  • Glomerular Mesangium / cytology
  • Glomerular Mesangium / enzymology*
  • Kidney Cortex / chemistry
  • Kidney Cortex / cytology
  • Kidney Cortex / enzymology
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins*
  • Molecular Sequence Data
  • Monoamine Oxidase / analysis
  • Monoamine Oxidase / metabolism*
  • Monoamine Oxidase Inhibitors / pharmacology
  • Nerve Tissue Proteins*
  • Pargyline / pharmacology
  • Rats
  • Serotonin / metabolism*
  • Serotonin / pharmacokinetics
  • Serotonin Plasma Membrane Transport Proteins

Substances

  • Antimetabolites
  • Carbon Radioisotopes
  • Carrier Proteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Monoamine Oxidase Inhibitors
  • Nerve Tissue Proteins
  • Serotonin Plasma Membrane Transport Proteins
  • Slc6a4 protein, rat
  • Serotonin
  • Pargyline
  • Monoamine Oxidase
  • Bromodeoxyuridine