Experimental & Applied Acarology

, Volume 9, Issue 3, pp 279–287

Hemocytic encapsulation of implants in the tickDermacentor variabilis

Authors

  • Lisa R. Eggenberger
    • Center for Electron Microscopy, Dept. of BiologyMemphis State University
  • William J. Lamoreaux
    • Center for Electron Microscopy, Dept. of BiologyMemphis State University
  • Lewis B. Coons
    • Center for Electron Microscopy, Dept. of BiologyMemphis State University
Article

DOI: 10.1007/BF01193434

Cite this article as:
Eggenberger, L.R., Lamoreaux, W.J. & Coons, L.B. Exp Appl Acarol (1990) 9: 279. doi:10.1007/BF01193434

Abstract

Implants of Epon, inserted inDermacentor variabilis (Say) through incisions in the cuticle, were encapsulated by hemocytes. We followed this process at intervals of 1, 3, 6, 12 and 24 h, and every 24 h thereafter up to 120 h. Degranulation of Type 1 granulocytes and coagulation of hemolymph were first seen at 1 h after implantation and were the earliest evidence of encapsulation. By 3 h after implantation, the degranulation and disintegration of granulocytes had formed a matrix at the Epon surface. From 6 h until encapsulation was completed, plasmatocytes and granulocytes continued to respond to degranulation and formed multiple cell layers around the Epon implant. The capsule was complete at 72 h after implantation. Completion was marked by decreasing degranulation, migration of hemocytes from the outermost layers of the capsule, and by the appearance of loosely attached hemocytes on the outer surface of the capsule. The most common junctional complex observed was gap junctions.

Copyright information

© Elsevier Science Publishers B.V 1990