Skip Navigation


JXB Advance Access originally published online on August 23, 2005
Journal of Experimental Botany 2005 56(420):2619-2628; doi:10.1093/jxb/eri256
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Supplementary videos
Right arrow All Versions of this Article:
56/420/2619    most recent
eri256v1
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Lazzaro, M. D.
Right arrow Articles by Hepler, P. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lazzaro, M. D.
Right arrow Articles by Hepler, P. K.
Agricola
Right arrow Articles by Lazzaro, M. D.
Right arrow Articles by Hepler, P. K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press [on behalf of the Society for Experimental Biology]. All rights reserved. For Permissions, please e-mail: journals.permissions@oupjournals.org

RESEARCH PAPER

Calcium gradients in conifer pollen tubes; dynamic properties differ from those seen in angiosperms

Mark D. Lazzaro1,*, Luis Cardenas2 {dagger}, Aadra P. Bhatt1 {ddagger}, Charles D. Justus1 {ddagger}, Monique S. Phillips1 {ddagger}, Terena L. Holdaway-Clarke2 § and Peter K. Hepler2

1Department of Biology, College of Charleston, Charleston, SC 29424, USA
2Department of Biology, University of Massachusetts, Amherst, MA 01003, USA

* To whom correspondence should be addressed. Fax: +1 843 953 5453. E-mail: lazzarom{at}cofc.edu

Pollen tubes are an established model system for examining polarized cell growth. The focus here is on pollen tubes of the conifer Norway spruce (Picea abies, Pinaceae); examining the relationship between cytosolic free Ca2+, tip elongation, and intracellular motility. Conifer pollen tubes show important differences from their angiosperm counterparts; they grow more slowly and their organelles move in an unusual fountain pattern, as opposed to reverse fountain, in the tip. Ratiometric ion imaging of growing pollen tubes, microinjected with fura-2-dextran, reveals a tip-focused [Ca2+]i gradient extending from 450 nM at the extreme apex to 225 nM at the base of the tip clear zone. Injection of 5,5' dibromo-BAPTA does not dissipate the apical gradient, but stops cell elongation and uniquely causes rapid, transient increases of apical free Ca2+. The [Ca2+]i gradient is, however, dissipated by reversible perfusion of extracellular caffeine. When the basal cytosolic free Ca2+ concentration falls below 150 nM, again a large increase in apical [Ca2+]i occurs. An external source of calcium is not required for germination but significantly enhances elongation. However, both germination and elongation are significantly inhibited by the inclusion of calcium channels blockers, including lanthanum, gadolinium, or verapamil. Modulation of intracellular calcium also affects organelle position and motility. Extracellular perfusion of lanthanides reversibly depletes the apical [Ca2+]i gradient, altering organelle positioning in the tip. Later, during recovery from lanthanide perfusion, organelle motility switches direction to a reverse fountain. When taken together these data show a unique interplay in Picea abies pollen tubes between intracellular calcium and the motile processes controlling cellular organization.

Key words: Calcium, conifer, Picea abies, pollen tube


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Am. J. Bot.Home page
J. H. Williams
Amborella trichopoda (Amborellaceae) and the evolutionary developmental origins of the angiosperm progamic phase
Am. J. Botany, January 1, 2009; 96(1): 144 - 165.
[Abstract] [Full Text] [PDF]


Home page
ANN BOT (LOND)Home page
T. J. Bushart and S. J. Roux
Conserved Features of Germination and Polarized Cell Growth: A Few Insights from a Pollen-Fern Spore Comparison
Ann. Bot., January 1, 2007; 99(1): 9 - 17.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
T. Chen, N. Teng, X. Wu, Y. Wang, W. Tang, J. Samaj, F. Baluska, and J. Lin
Disruption of Actin Filaments by Latrunculin B Affects Cell Wall Construction in Picea meyeri Pollen Tube by Disturbing Vesicle Trafficking
Plant Cell Physiol., January 1, 2007; 48(1): 19 - 30.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.