spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in JEB
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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Blackstone, N. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Blackstone, N. W.
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   Add to Twitter  
What's this?
The Journal of Experimental Biology 206, 651-658 (2003)
doi: 10.1242/jeb.00138

Redox signaling in the growth and development of colonial hydroids

Neil W. Blackstone

Department of Biological Sciences, Northern Illinois University, DeKalb, IL 60115, USA

(e-mail: neilb{at}niu.edu)

Accepted 6 November 2002

Redox signaling provides a quick and efficient mechanism for clonal or colonial organisms to adapt their growth and development to aspects of the environment, e.g. the food supply. A `signature' of mitochondrial redox signaling, particularly as mediated by reactive oxygen species (ROS), can be elucidated by experimental manipulation of the electron transport chain. The major sites of ROS formation are found at NADH dehydrogenase of complex I and at the interface between coenzyme Q and complex III. Inhibitors of complex III should thus upregulate ROS from both sites; inhibitors of complex I should upregulate ROS from the first but not the second site, while uncouplers of oxidative phosphorylation should downregulate ROS from both sites. To investigate the possibility of such redox signaling, perturbations of colony growth and development were carried out using the hydroid Podocoryna carnea. Oxygen uptake of colonies was measured to determine comparable physiological doses of antimycin A1 (an inhibitor of complex III), rotenone (an inhibitor of complex I) and carbonyl cyanide m-chlorophenylhydrazone (CCCP; an uncoupler of oxidative phosphorylation). Using these doses, clear effects on colony growth and development were obtained. Treatment with antimycin A1 results in `runner-like' colony growth, with widely spaced polyps and stolon branches, while treatment with CCCP results in `sheet-like' growth, with closely spaced polyps and stolon branches. Parallel results have been obtained previously with azide, an inhibitor of complex IV, and dinitrophenol, another uncoupler of oxidative phosphorylation. Perhaps surprisingly, rotenone produced effects on colony development similar to those of CCCP. Assays of peroxides using 2',7'-dichlorofluorescin diacetate and fluorescent microscopy suggest a moderate difference in ROS formation between the antimycin and rotenone treatments. The second site of ROS formation (the interface between coenzyme Q and complex III) may thus predominate in the signaling that regulates colony development. The fat-rich, brine shrimp diet of these hydroids may be relevant in this context. Acyl CoA dehydrogenase, which catalyzes the first step in the mitochondrial ß-oxidation of fatty acids, carries electrons to coenzyme Q, thus bypassing complex I. These results support a role for redox signaling, mediated by ROS, in colony development. Nevertheless, other redox sensors between complexes I and III may yet be found.

Key words: clonal, colony development, evolutionary morphology, hydroid, Podocoryna, Podocoryne, reactive oxygen species, redox signaling


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   Add to Twitter Twitter    What's this?

Related articles in JEB:

ROS RELOCATES MOUTHS
Kathryn Phillips
JEB 2003 206: 638. [Full Text]  



This article has been cited by other articles:


Home page
JCBHome page
L. S. Terada
Specificity in reactive oxidant signaling: think globally, act locally
J. Cell Biol., August 28, 2006; 174(5): 615 - 623.
[Abstract] [Full Text] [PDF]


Home page
Integr. Comp. Biol.Home page
N. W. Blackstone and D. M. Bridge
Model Systems for Environmental Signaling
Integr. Comp. Biol., August 1, 2005; 45(4): 605 - 614.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
M. Habetha and T. C. G. Bosch
Symbiotic Hydra express a plant-like peroxidase gene during oogenesis
J. Exp. Biol., June 1, 2005; 208(11): 2157 - 2165.
[Abstract] [Full Text] [PDF]


Home page
Proc R Soc BHome page
N. W Blackstone, M. M Kelly, V. Haridas, and J. U Gutterman
Mitochondria as integrators of information in an early-evolving animal: insights from a triterpenoid metabolite
Proc R Soc B, March 7, 2005; 272(1562): 527 - 531.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
N. W. Blackstone, M. J. Bivins, K. S. Cherry, R. E. Fletcher, and G. C. Geddes
Redox signaling in colonial hydroids: many pathways for peroxide
J. Exp. Biol., January 15, 2005; 208(2): 383 - 390.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
K. Phillips
ROS RELOCATES MOUTHS
J. Exp. Biol., February 15, 2003; 206(4): 638 - 638.
[Full Text] [PDF]




© The Company of Biologists Ltd 2003