Journal of Histochemistry and Cytochemistry Priciples for Free Access to Science
  Search:   
    >> Advanced Search

Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact
JHC exPRESS: First Published July 24, 2006. doi:10.1369/jhc.6A6935.2006
Copyright © Histochemical Society, Inc.


A more recent version of this article appeared on October 1, 2006.
This Article
Right arrow exPRESS PDF
Right arrow All Versions of this Article:
jhc.6A6935.2006v1
54/10/1169    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hoshi, H.
Right arrow Articles by Mills, S. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hoshi, H.
Right arrow Articles by Mills, S. L.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Articles

A Novel Fluorescent Tracer for Visualizing Coupled Cells in Neural Circuits of Living Tissue

Hideo Hoshi 1, John O’Brien 1 and Stephen L. Mills 1*

1 Department of Ophthalmology and Visual Science, University of Texas at Houston - Health Science Center, Houston, Texas

* To whom correspondence should be addressed. E-mail: Stephen.L.Mills{at}uth.tmc.edu .

Submitted on January 30, 2006
Accepted on 12 July 2006


   Abstract
Gap junctions have diverse roles in a wide variety of tissues and have recently become a subject of intense investigation in neural circuits where synchrony and oscillations may play an important part. In circuits where gap junctions are present, the possibility arises of identifying intercommunicating cells via introduction of tracer into one cell and observing its spread into its coupled neighbors. Staining the coupled cells by this means opens the door to many vital techniques, including paired cell electrophysiology, RT-PCR, and morphological characterization of previously unknown coupled cells. The tracers commonly used at the present time are not in general suitable for these purposes in many tissues, including neurons. This paper describes how a fluorescent nuclear tracer, Po-pro-1, can be used to visualize coupled cells in several types of retinal neurons thought to be comprised of different connexin proteins, including Cx36, Cx45, Cx50 and Cx57.

Key Words: gap junction, connexin, electrical coupling, retina


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 Reddit Reddit   Add to Technorati Technorati    What's this?





Guidelines | Subscriptions | About | exPRESS - Current - Archive | Business Information | Contact
The Journal of Histochemistry & Cytochemistry is owned, published, and licensed by The Histochemical Society © 2006