Protein tyrosine phosphatase receptor type R deficient mice exhibit increased exploration in a new environment and

Mirthe Erkens1, Brenda Bakker1, Lucette M van Duijn1

  • 1Department of Cell Biology, Nijmegen Centre for Molecular Life Sciences, Radboud University Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

Behavioural Brain Research
|February 22, 2014
PubMed

Insights

Protein tyrosine phosphatase receptor type R (PTPRR) regulates brain MAPK signaling. Loss of PTPRR impairs novel object recognition and increases exploratory activity in mice.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • The mouse gene Ptprr encodes protein tyrosine phosphatase receptor type R (PTPRR) isoforms.
  • PTPRR negatively regulates mitogen-activated protein kinase (MAPK) signaling pathways.
  • PTPRR proteins are found in various mouse brain regions, including the cerebellum, olfactory bulb, hippocampus, amygdala, and perirhinal cortex.

Purpose of the Study:

  • To investigate the phenotypic consequences of PTPRR deficiency in mice.
  • To determine the role of PTPRR in specific brain functions, including olfaction, spatial learning, fear conditioning, novel object recognition, and exploratory behavior.

Main Methods:

  • Phenotypic evaluation of PTPRR-deficient mice (Ptprr(-/-)).
  • Assessment of basal smell, spatial learning, fear-associated contextual learning, novel object recognition, and exploratory activity.

Main Results:

  • Ptprr(-/-) mice exhibited normal basal smell, spatial learning, and fear-associated contextual learning.
  • PTPRR deficiency led to impaired novel object recognition.
  • A significant increase in exploratory activity in a novel environment was observed in Ptprr(-/-) mice.

Conclusions:

  • PTPRR plays a crucial role in regulating MAPK signaling in the brain.
  • PTPRR deficiency impacts specific cognitive functions, notably novel object recognition and exploratory behavior.
  • PTPRR is identified as a potential therapeutic target for modulating synaptic processes and related cerebral functions.