JCB logo
Avanti Polar Lipids, Inc.
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online
doi:10.1083/jcb.1836iti1
The Journal of Cell Biology, Vol. 183, No. 6, 964-
The Rockefeller University Press, 0021-9525 $30.00
© Williams
This Article
Right arrow Full Text (PDF, 769K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

In This Issue

Multiple axons and actions with PSD-95



Figure 1
More PSD-95 means bigger spines (top), and multiple axon connections.

Nitric oxide gets neurons together. And it seems to do it backward. Work by Nikonenko et al. suggests that a protein called PSD-95 prompts nitric oxide release from postsynaptic dendritic spines, prompting nearby presynaptic axons to lock on, and develop new synapses.

It is becoming increasingly clear that synaptogenesis is not solely axon driven. PSD-95 is a major component of postsynaptic densities—a conglomeration of scaffolding proteins, neurotransmitter receptors, and signaling proteins that are thought to shape dendritic spines—and reduced levels of PSD-95 impair synapse development. How PSD-95 works, however, was unknown.

Nikonenko et al. overexpressed PSD-95 in cultured hippocampal neurons and found that the cells' dendritic spines grew two to three times their normal size and were often contacted by multiple axons—a rare occurrence in the adult brain. By mutating different parts of PSD-95, the team discovered that the region responsible for prompting multi-axon connections was also required for binding nitrogen oxide synthase. The team cut to the chase, bathed neurons in nitric oxide, and showed this was sufficient to promote the extra axon connections. Since bathing cells in nitric oxide and overexpressing proteins do not reflect normal physiological conditions, the team also inhibited nitric oxide synthase in wild-type neurons and confirmed that synapse density was reduced.

Overexpressing PSD-95 increased the amount of nitric oxide synthase at postsynaptic densities, suggesting PSD-95 recruits the synthase to its required locale. Interestingly, PSD-95 that lacked its synthase interaction domain still induced super-sized dendritic spines, suggesting PSD-95 wears more than one hat at the synapse construction site. RW

Nikonenko, I., et al. 2008. J. Cell Biol. doi:10.1083/jcb.200805132.[Abstract/Free Full Text]



Ruth Williams

ruth.williams{at}rockefeller.edu


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?



This Article
Right arrow Full Text (PDF, 769K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents