Differential in vitro effects of insulin on Taenia crassiceps and Taenia solium cysticerci

J Helminthol. 2009 Dec;83(4):403-12. doi: 10.1017/S0022149X09990265. Epub 2009 Jun 24.

Abstract

Hormones play a significant role in murine cysticercosis (Taenia crassiceps), and increase the frequency of porcine cysticercosis caused by Taenia solium. In the present study, we report the in vitro effect of insulin on the larval stages of T. crassiceps (ORF strain) and T. solium. In vitro exposure of T. crassiceps cysticerci to insulin was found to stimulate this parasite's reproduction twofold with respect to control values, while the same treatment had no effect on T. solium cysticerci. Moreover, normal female mice (BALB/cAnN) infected with T. crassiceps cysticerci previously exposed to insulin presented larger parasite loads than mice inoculated with vehicle-treated cysticerci. To determine the possible molecular mechanisms by which insulin affects T. crassiceps, the insulin receptor was amplified by means of reverse transcriptase-polymerase chain reaction (RT-PCR). Interestingly, both T. crassiceps and T. solium expressed the insulin receptor, although insulin had effects only on T. crassiceps. These results demonstrate that insulin has a dichotomistic effect; it acts directly only on T. crassiceps cysticerci reproduction, possibly through its binding to a specific insulin receptor synthesized by the parasite. Thus, insulin may be recognized by T. crassiceps cysticercus cells as a mitogenic factor, and contribute to parasite proliferation inside the host, as well as to the female mouse susceptibility to T.crassiceps. This phenomenon has not been reported for cysticercosis caused by T. solium, which could, in part, be related to the poor effect of insulin upon the human parasite.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Helminth / immunology*
  • Cysticercus / immunology*
  • Cysticercus / pathogenicity
  • DNA, Helminth
  • Female
  • Hormones
  • Host-Pathogen Interactions
  • Insulin / pharmacology*
  • Mice
  • Mice, Inbred BALB C / immunology
  • Mice, Inbred BALB C / parasitology*
  • RNA, Messenger
  • Receptor, Insulin
  • Reverse Transcriptase Polymerase Chain Reaction
  • Taenia solium / immunology*
  • Taenia solium / pathogenicity

Substances

  • Antigens, Helminth
  • DNA, Helminth
  • Hormones
  • Insulin
  • RNA, Messenger
  • Receptor, Insulin