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 Full Text (PDF)
Right arrow References
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 Similar articles in this journal
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 Churchill, D.
Right arrow Articles by Caveney, S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Churchill, D.
Right arrow Articles by Caveney, S.

Journal of Cell Science, Vol 104, Issue 3 763-772, Copyright © 1993 by Company of Biologists


RESEARCH ARTICLE

Rapid de novo formation of gap junctions between insect hemocytes in vitro: a freeze-fracture, dye- transfer and patch-clamp study

D. Churchill, S. Coodin, R. R. Shivers and S. Caveney

Gap junctions form between insect hemocytes (blood cells) when they encapsulate foreign objects in the hemocoel (body cavity). In this study we show that hemocytes from cockroach (Periplaneta americana) form gap-junctions rapidly in vitro. Freeze-fracture replicas of hemocyte aggregates fixed 5 minutes after bleeding contain gap-junctional plaques. Dye passage was detected between carboxyfluorescein diacetate- labelled and unlabelled hemocytes within 3 minutes of bleeding, when the cells made contact as they flattened rapidly onto coverslips. When double whole-cell voltage-clamp was used to measure gap-junction formation between cells which were pushed together, electrical coupling was detected within one second of cell-cell contact. To prevent extensive flattening, cells were plated onto lipophorin-coated coverslips. Junctional conductance increased in staircase fashion with steps corresponding to an average single channel conductance of 345 pS. Assuming all channels to have this conductance, the maximal accretion rate of channels to the growing junction was one channel per second. Junctional currents and dye-coupling were detected in the absence of Ca2+, indicating that involvement of Ca2+-dependent adhesion molecules is not a prerequisite for gap-junction formation in hemocytes. Hemocytes from distantly related insects (cockroach and moth) form functional gap junctions with each other, suggesting sequence homology among gap- junction proteins in insects. The function of rapid gap-junction formation between hemocytes during encapsulation and wound healing in vivo are discussed.


This article has been cited by other articles:


Home page
Circ. Res.Home page
V. Valiunas, F. F. Bukauskas, and R. Weingart
Conductances and Selective Permeability of Connexin43 Gap Junction Channels Examined in Neonatal Rat Heart Cells
Circ. Res., May 19, 1997; 80(5): 708 - 719.
[Abstract] [Full Text]




© The Company of Biologists Ltd 1993