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

Published 23 October 2006. doi:10.1083/jcb.1752iti1
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 175, Number 2, 194-194
This Article
Right arrow Full Text (PDF, 1670K)
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 Leslie, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Leslie, M.
Related Collections
Right arrowRelated Article
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

Taking a Toll on neurons



Figure 1
Toll-like receptor 8 (green) restrains cortical neurons in the mouse embryo.

Battling pathogens and shaping neuronal growth seem to have as much in common as accounting and skydiving. But both tasks involve one of the Toll-like proteins, as Ma et al. report on page 209. The study is the first to discover a function for a member of the Toll-like family within neurons.

Toll-like receptors (TLRs) enable mammalian immune cells to identify interlopers. TLR8, for instance, recognizes RNA on the loose, a sign of viral infection or cell destruction. The Drosophila equivalents of the proteins, the Toll receptors, also supervise synapse formation and axon growth, researchers have discovered. Although previous studies had revealed that mammalian neurons manufacture TLRs, no one had shown that the molecules performed a job in these cells.

Ma et al. found that brain levels of TLR8 shot up in the early mouse embryo and fell after birth, suggesting that the molecule participates in nervous system development. To clarify its role, the researchers dosed embryonic brain cells with a compound that stimulates TLR8. The treatment impeded the growth of neurites, the branches that sprout from developing neurons, and spurred some of the cells to kill themselves. An antibody that latches onto TLR8 prevented both effects.

TLR8 usually raises the alarm by activating the signaling pathway headed by NF-{kappa}B. But Ma et al. showed that NF-{kappa}B remained off in neurons, indicating that the receptor acts in these cells through an unidentified pathway. The researchers speculate that TLR8 might serve as a danger detector in neurons. If it senses infection or tissue damage, it may deter neurons from entering the trouble spot by pruning their neurites or triggering their suicide. Formula



Mitch Leslie

mitchleslie{at}comcast.net


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?

Related Article

Toll-like receptor 8 functions as a negative regulator of neurite outgrowth and inducer of neuronal apoptosis
Yinghua Ma, Jianxue Li, Isaac Chiu, Yawen Wang, Jacob A. Sloane, Jining Lü, Bela Kosaras, Richard L. Sidman, Joseph J. Volpe, and Timothy Vartanian
J. Cell Biol. 2006 175: 209-215. [Abstract] [Full Text] [PDF]




This Article
Right arrow Full Text (PDF, 1670K)
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 Leslie, M.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Leslie, M.
Related Collections
Right arrowRelated Article
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