Difference between revisions of "Neurotrophins"

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(Created page with '==Neurotrophins== Neurotrophins are responsible primarily for the regulation of cell proliferation, migration, and survival. They also have a hand in the modulation of axonal a…')
 
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Neurotrophins are responsible primarily for the regulation of cell proliferation, migration, and survival.  They also have a hand in the modulation of axonal and dendritic outgrowth, and synapse formation.  They have an abnormal expression patter in autistic patients.   
 
Neurotrophins are responsible primarily for the regulation of cell proliferation, migration, and survival.  They also have a hand in the modulation of axonal and dendritic outgrowth, and synapse formation.  They have an abnormal expression patter in autistic patients.   
  
BDNF, a neurotrophin, and its receptor, trkB, are expressed in cortical and hippocampal neurons and influences axonal and dendritic growth in a neuro specific and age-dependent manner.  BDNF abnormalities have been implicated in schizophrenia and depression, brain disorders which show altered cortical maturation and plasticity. Some studies have found elevated levels of BDNF and NT4/5 in neonatal blood samples of ASD patients.  One study found elevated levels of of BDNF along with auto-antibodies against BDNF.  There is some evidence that BDNF regulation abnormalities could be a primary factor in autism development from a study on the gene CADPS2, which controls the exocytosis of BDNF-containing vesicles.  It was found that CADPS2 was differently spliced in some autistic patients and that CADPS2 knockout mice have autistic-like phenotypes.   
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BDNF, a neurotrophin, and its receptor, trkB, are expressed in cortical and hippocampal neurons and influences axonal and dendritic growth in a neuro specific and age-dependent manner.  BDNF abnormalities have been implicated in schizophrenia and depression, brain disorders which show altered cortical maturation and plasticity. Some studies have found elevated levels of BDNF and NT4/5 in neonatal blood samples of ASD patients.  One study found elevated levels of of BDNF along with auto-antibodies against BDNF.  There is some evidence that BDNF regulation abnormalities could be a primary factor in autism development from a study on the gene CADPS2, which controls the exocytosis of BDNF-containing vesicles.  It was found that CADPS2 was differently spliced in some autistic patients and that CADPS2 knockout mice have autistic-like phenotypes.<sup>1</sup>  
  
  
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====References====
 
====References====
 
1. Pardo, CA et. al.  '''The Neurobiology of Autism.'''Brain Pathol. 2007 Oct;17(4):434-47. PMID 17919129
 
1. Pardo, CA et. al.  '''The Neurobiology of Autism.'''Brain Pathol. 2007 Oct;17(4):434-47. PMID 17919129
 
2. Fatemi SH.  '''Reelin glycoprotein: structure, biology and roles in health and disease.''' Mol Psychiatry. 2005 Mar;10(3):251-7. PMID 15583703
 
 
3. Fatemi SH.  '''Reelin glycoprotein in autism and schizophrenia.'''Int Rev Neurobiol. 2005;71:179-87. PMID 16512351
 

Revision as of 16:54, 17 November 2009

Neurotrophins

Neurotrophins are responsible primarily for the regulation of cell proliferation, migration, and survival. They also have a hand in the modulation of axonal and dendritic outgrowth, and synapse formation. They have an abnormal expression patter in autistic patients.

BDNF, a neurotrophin, and its receptor, trkB, are expressed in cortical and hippocampal neurons and influences axonal and dendritic growth in a neuro specific and age-dependent manner. BDNF abnormalities have been implicated in schizophrenia and depression, brain disorders which show altered cortical maturation and plasticity. Some studies have found elevated levels of BDNF and NT4/5 in neonatal blood samples of ASD patients. One study found elevated levels of of BDNF along with auto-antibodies against BDNF. There is some evidence that BDNF regulation abnormalities could be a primary factor in autism development from a study on the gene CADPS2, which controls the exocytosis of BDNF-containing vesicles. It was found that CADPS2 was differently spliced in some autistic patients and that CADPS2 knockout mice have autistic-like phenotypes.1






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References

1. Pardo, CA et. al. The Neurobiology of Autism.Brain Pathol. 2007 Oct;17(4):434-47. PMID 17919129