A non-expressed transgene as a cell marker for the investigation of cellular traffic after splenic autotransplantation

J Immunol Methods. 1996 Aug 14;194(2):131-9. doi: 10.1016/0022-1759(96)00062-2.

Abstract

The investigation of cellular interactions during the regeneration of splenic transplants depends upon distinguishing host cells from graft derived cells. As a cell marker which, in contrast to many other marker systems, does not affect histocompatibility, the non-expressed transgene mMT-HGHRH-1 was introduced by mating into NMRI inbred mice to generate the transgenic mouse line BSM. By transplanting non-transgenic NMRI splenic tissue into transgenic BSM hosts, host derived cells could be identified in the transplants by in situ hybridization after regeneration. In a reciprocal approach, implant derived cells were detected in a transgenic transplant after 3 weeks of regeneration in a non-transgenic host. Relative amounts of transgenic cells in transplant cross-sections were estimated from the signal intensity of autoradiographs by densitometry and computer analysis. This approach could be broadly applied in studies of transplantation systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Survival
  • Chromatin / chemistry
  • Female
  • Gene Expression
  • Genetic Markers
  • In Situ Hybridization
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mice, Transgenic
  • Regeneration / physiology*
  • Sensitivity and Specificity
  • Spleen / cytology
  • Spleen / physiology*
  • Spleen / transplantation*
  • Transgenes*

Substances

  • Chromatin
  • Genetic Markers