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Functional Calcium Imaging in Developing Cortical Networks
Published on: October 22, 2011
Regulation of complexin 1 and complexin 2 in the developing human prefrontal cortex
Kayvon Salimi1, Leisa A Glantz, Robert M Hamer
1Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Synapse (New York, N.Y.)
|February 2, 2008
Summary
Complexin 1 and complexin 2 protein levels increase during human brain development, indicating a shift towards more inhibitory synapses in the prefrontal cortex during maturation.
Area of Science:
- Neuroscience
- Developmental Biology
- Synaptic Plasticity
Background:
- Complexins (CX1 and CX2) are key presynaptic proteins regulating neurotransmitter release.
- CX1 and CX2 serve as markers for excitatory and inhibitory synapses, respectively.
- Understanding synaptic development in the human prefrontal cortex (PFC) is crucial for cognitive function.
Purpose of the Study:
- To investigate the developmental trajectory of inhibitory and excitatory synapses in the human PFC.
- To examine the expression patterns of CX1 and CX2 during human brain development.
Main Methods:
- Western blotting was used to quantify CX1 and CX2 protein levels.
- Postmortem dorsolateral prefrontal cortex (DLPFC) samples from 42 individuals (18 weeks gestation to 25 years) were analyzed.
- Samples were grouped by age: fetal, infant, child, adolescent, and young adult.
Main Results:
- CX1 levels increased progressively throughout development, from fetal to young adult stages.
- CX2 levels increased from fetal to childhood and then plateaued.
- The CX2/CX1 ratio, indicative of inhibitory to excitatory synapse balance, was higher in fetal and infant groups compared to young adults.
Conclusions:
- Complexin expression and synaptic maturation increase during human DLPFC development.
- The balance of synaptic influence shifts towards inhibition relative to excitation during development in this brain region.
- These findings provide insights into the developmental neurobiology of synaptic function in the human PFC.

