7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Conditional macrophage ablation in transgenic mice expressing a Fas-based suicide gene.

      Journal of Leukocyte Biology
      Animals, Antigens, CD95, genetics, Apoptosis, drug effects, Bacterial Infections, immunology, physiopathology, Cell Count, Cells, Cultured, Dendritic Cells, cytology, metabolism, Dimerization, Disease Models, Animal, Genes, Transgenic, Suicide, Green Fluorescent Proteins, Immunity, Cellular, Luminescent Proteins, Macrophages, Mice, Mice, Inbred C57BL, Mice, Transgenic, Promoter Regions, Genetic, Receptor, Macrophage Colony-Stimulating Factor, Receptors, Nerve Growth Factor, Tacrolimus, analogs & derivatives, pharmacology, Tacrolimus Binding Proteins

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Transgenic mice expressing an inducible suicide gene, which allows systemic and reversible elimination of macrophages, were developed. A macrophage-specific c-fms promoter was used to express enhanced green fluorescent protein and a drug-inducible suicide gene that leads to Fas-mediated apoptosis in resting and cycling cells of the macrophage lineage. Transgenic mice were fertile, of normal weight, and showed no abnormal phenotype before drug exposure. The transgene was expressed constitutively in macrophages and dendritic cells (DC) but not significantly in T cells or B cells. Induction of the suicide gene led to depletion of 70-95% of macrophages and DC in nearly all tissues examined. Depletion reduced the ability to clear bacteria from the blood and led to increased bacterial growth in the liver. Depleted mice displayed several abnormalities, including splenomegaly, lymphadenopathy, thymic atrophy, extramedullary hematopoiesis, and development of peritoneal adhesions. This new, transgenic line will be useful in investigating the role of macrophages and DC.

          Related collections

          Author and article information

          Comments

          Comment on this article