|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
Journal of Cell Science, Vol 109, Issue 8 2053-2060, Copyright © 1996 by Company of Biologists
JOURNAL ARTICLES |
LL Pech and MR Strand
Department of Entomology, University of Wisconsin-Madison 53706, USA.
Haemocytes play an essential role in defending invertebrates against pathogens and parasites that enter their haemocoel. A primary defense response is encapsulation; a process in which haemocytes attach to the foreign organism and kill it. Whether encapsulation requires cooperation between specific subpopulations of haemocytes is unknown. Using purified subpopulations of haemocytes and an in vitro encapsulation assay, we investigated the process of capsule formation in the insect Pseudoplusia includens. Immunocytochemical staining revealed that capsule formation involves a three step process. Encapsulation began when granular cells attached to the foreign target. This was followed by attachment of multiple layers of plasmatocytes. Termination of capsule formation occurred when a subpopulation of granular cells formed a monolayer around the periphery of the capsule. Neither granular cells nor plasmatocytes were capable of forming a capsule independently. However, plasmatocytes encapsulated targets if granular cells were present or if targets were preincubated in medium conditioned by granular cells. The effect of granular cell-conditioned medium could be blocked by the addition of the cell adhesion recognition sequence, RGDS, but not by RGES. These results demonstrate experimentally that granular cells are required for encapsulation of foreign targets by plasmatocytes in vitro, and that the role of granular cells in this process involves an RGD-dependent cell adhesion mechanism.
This article has been cited by other articles:
![]() |
D. T. Babcock, A. R. Brock, G. S. Fish, Y. Wang, L. Perrin, M. A. Krasnow, and M. J. Galko Circulating blood cells function as a surveillance system for damaged tissue in Drosophila larvae PNAS, July 22, 2008; 105(29): 10017 - 10022. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Suderman, A. J. Pruijssers, and M. R. Strand Protein tyrosine phosphatase-H2 from a polydnavirus induces apoptosis of insect cells J. Gen. Virol., June 1, 2008; 89(6): 1411 - 1420. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Pruijssers and M. R. Strand PTP-H2 and PTP-H3 from Microplitis demolitor Bracovirus Localize to Focal Adhesions and Are Antiphagocytic in Insect Immune Cells J. Virol., February 1, 2007; 81(3): 1209 - 1219. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Vergote, P.-E. Sautiere, F. Vandenbulcke, D. Vieau, G. Mitta, E. R. Macagno, and M. Salzet Up-regulation of Neurohemerythrin Expression in the Central Nervous System of the Medicinal Leech, Hirudo medicinalis, following Septic Injury J. Biol. Chem., October 15, 2004; 279(42): 43828 - 43837. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. D. Clark, S. F. Garczynski, A. Arora, J. W. Crim, and M. R. Strand Specific Residues in Plasmatocyte-spreading Peptide Are Required for Receptor Binding and Functional Antagonism of Insect Immune Cells J. Biol. Chem., August 6, 2004; 279(32): 33246 - 33252. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. A. Whitten, I. F. Tew, B. L. Lee, and N. A. Ratcliffe A Novel Role for an Insect Apolipoprotein (Apolipophorin III) in {beta}-1,3-Glucan Pattern Recognition and Cellular Encapsulation Reactions J. Immunol., February 15, 2004; 172(4): 2177 - 2185. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. J. Daborn, N. Waterfield, C. P. Silva, C. P. Y. Au, S. Sharma, and R. H. ffrench-Constant A single Photorhabdus gene, makes caterpillars floppy (mcf), allows Escherichia coli to persist within and kill insects PNAS, August 6, 2002; 99(16): 10742 - 10747. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Trudeau, R. A. Witherell, and M. R. Strand Characterization of two novel Microplitis demolitor polydnavirus mRNAs expressed in Pseudoplusia includens haemocytes J. Gen. Virol., December 1, 2000; 81(12): 3049 - 3058. [Abstract] [Full Text] |
||||
![]() |
K. D. Clark, L. L. Pech, and M. R. Strand Isolation and Identification of a Plasmatocyte-spreading Peptide from the Hemolymph of the Lepidopteran Insect Pseudoplusia includens J. Biol. Chem., September 12, 1997; 272(37): 23440 - 23447. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. D. Clark, B. F. Volkman, H. Thoetkiattikul, Y. Hayakawa, and M. R. Strand N-terminal Residues of Plasmatocyte-spreading Peptide Possess Specific Determinants Required for Biological Activity J. Biol. Chem., September 28, 2001; 276(40): 37431 - 37435. [Abstract] [Full Text] [PDF] |
||||