Splenic and immune alterations of the Sparc-null mouse accompany a lack of immune response

Genes Immun. 2007 Apr;8(3):262-74. doi: 10.1038/sj.gene.6364388. Epub 2007 Mar 8.

Abstract

Sparc-null mice have been used as models to assess tumor-host immune cell interactions. However, it is not known if they have a competent immune system. In this study, the immune systems of Sparc wild-type and null mice were compared. Mice were assessed for differences in total body weight, spleen weight and spleen-to-body weight ratios. Spleens were compared with respect to morphology, and Sparc, Ki-67, MOMA-1 and IgM expression. Immune cells in blood, bone marrow and spleen were assessed by blood smears, automated blood panel, and flow cytometry. Additionally, the ability of Sparc-null mice to respond to immune challenge was evaluated using a footpad model. The morphological and immunohistochemical results indicated that Sparc-null spleens had more white pulp, hyperproliferative B cells in the germinal centers, and decreased marginal zones. Sparc-null spleens lacked normal Sparc expression in red and white pulp, marginal zones, endothelial and sinusoidal cells. By flow analysis, B cells were decreased and T cells were increased in the bone marrow. Finally, Sparc-null mice were unable to mount an immune response following footpad lipopolysaccharide challenge. These data confirm that Sparc-null mice have an impaired immune system.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Base Sequence
  • Body Weight
  • DNA Primers / genetics
  • Flow Cytometry
  • Gene Expression
  • Immune Tolerance
  • Lymphocytes / cytology
  • Lymphocytes / immunology
  • Lymphocytes / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Organ Size
  • Osteonectin / deficiency*
  • Osteonectin / genetics
  • Osteonectin / immunology*
  • Osteonectin / metabolism
  • Spleen / anatomy & histology
  • Spleen / immunology*
  • Spleen / metabolism

Substances

  • DNA Primers
  • Osteonectin