Expression of glutamate carboxypeptidase II in human brain

Neuroscience. 2007 Feb 23;144(4):1361-72. doi: 10.1016/j.neuroscience.2006.10.022. Epub 2006 Dec 5.


Glutamate carboxypeptidase II (GCPII) is a transmembrane glycoprotein expressed in various tissues. When expressed in the brain it cleaves the neurotransmitter N-acetylaspartylglutamate (NAAG), yielding free glutamate. In jejunum it hydrolyzes folylpoly-gamma-glutamate, thus facilitating folate absorption. The prostate form of GCPII, known as prostate specific membrane antigen (PSMA), is an established cancer marker. The NAAG-hydrolyzing activity of GCPII has been implicated in a number of pathological conditions in which glutamate is neurotoxic (e.g. amyotrophic lateral sclerosis, Huntington's disease, Alzheimer's disease, epilepsy, schizophrenia, and stroke). Inhibition of GCPII was shown to be neuroprotective in tissue culture and in animal models. GCPII is therefore an interesting putative therapeutic target. However, only very limited and controversial data on the expression and localization of GCPII in human brain are available. Therefore, we set out to analyze the activity and expression of GCPII in various compartments of the human brain using a radiolabeled substrate of the enzyme and the novel monoclonal antibody GCP-04, which recognizes an epitope on the extracellular portion of the enzyme and is more sensitive to GCPII than to the homologous GCPIII. We show that this antibody is more sensitive in immunoblots than the widely used antibody 7E11. By Western blot, we show that there are approximately 50-300 ng of GCPII/mg of total protein in human brain, depending on the specific area. Immunohistochemical analysis revealed that astrocytes specifically express GCPII in all parts of the brain. GCPII is enzymatically active and the level of activity follows the expression pattern. Using pure recombinant GCPII and homologous GCPIII, we conclude that GCPII is responsible for the majority of overall NAAG-hydrolyzing activity in the human brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antibodies / immunology
  • Antigens, Surface / analysis
  • Antigens, Surface / immunology
  • Antigens, Surface / metabolism*
  • Astrocytes / enzymology
  • Blotting, Western
  • Brain / anatomy & histology
  • Brain / enzymology*
  • Dipeptides / metabolism*
  • Enzyme Activation / physiology
  • Epitope Mapping / methods
  • Female
  • Glutamate Carboxypeptidase II / analysis
  • Glutamate Carboxypeptidase II / immunology
  • Glutamate Carboxypeptidase II / metabolism*
  • Glutamic Acid / biosynthesis*
  • Humans
  • Immunohistochemistry / methods
  • Male
  • Middle Aged
  • Models, Molecular
  • Protein Structure, Tertiary / physiology
  • Radioligand Assay / methods
  • Recombinant Fusion Proteins / metabolism


  • Antibodies
  • Antigens, Surface
  • Dipeptides
  • Recombinant Fusion Proteins
  • isospaglumic acid
  • Glutamic Acid
  • FOLH1 protein, human
  • Glutamate Carboxypeptidase II