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 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 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 DAVIES, P. S.
Right arrow Articles by PARTRIDGE, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by DAVIES, P. S.
Right arrow Articles by PARTRIDGE, T.

Journal of Cell Science, Vol 11, 757-769, Copyright © 1972 by Company of Biologists

Limpet Haemocytes

I. Studies on Aggregation and Spike Formation

P. S. DAVIES 1 and T. PARTRIDGE 2

1 Department of Zoology and Department of Cell Biology, University of Glasgow, Glasgow, Scotland
2 Department of Zoology and Department of Cell Biology, University of Glasgow, Glasgow, Scotland; Department of Experimental Pathology, Charing Cross Hospital Medical School, London W6, England

In this paper a promising new spontaneously aggregating system of amoebocytes from the blood of limpets is described. The system has the advantage of being readily available without cell culture and of being operational at room temperature.

The blood of the limpet Patella contains 2 types of haemocytes, amoebocytes and macro-phages, the latter accounting for less than 1 % of the cell population. The concentration of cells in suspension varies with the body temperature of the animal, from about 1 x 106 cells/ml at 5 °C to 9 x 106 cells/ml at 25 °C.

Following blood withdrawal the amoebocytes are approximately spherical in shape with superficial convoluted lamellae, but over a period of 5 min develop stout marginal spikes. This development is temperature dependent and independent of divalent cations in the medium.

Most interestingly, and apparently associated with the stimulus of blood withdrawal, the cells become spontaneously adhesive and commence an extremely rapid aggregation. With a shaking speed of 700 strokes/min the half time of aggregation varies from 15 s at an initial cell density of 4.7 x 106 cells/ml to 60 s at a density of 1.4 x 106 cells/ml. The aggregates so formed are very resistant to mechanical dispersion and tight junctions have been observed between aggregated cells in electron micrographs. Complete aggregation requires the presence of divalent cations and another unidentified plasma component. Aggregation will occur at 0 °C but the process is slower and less complete than at 20 °C. It is suggested that aggregation involves the triggering or activation of a pre-synthesized adhesive system and that the adhesiveness per unit area increases with increase in temperature.







© The Company of Biologists Ltd 1972