| First Author | Vieten G | Year | 1992 |
| Journal | Clin Immunol Immunopathol | Volume | 65 |
| Issue | 3 | Pages | 212-8 |
| PubMed ID | 1451327 | Mgi Jnum | J:3396 |
| Mgi Id | MGI:51909 | Doi | 10.1016/0090-1229(92)90149-i |
| Citation | Vieten G, et al. (1992) Expanded macrophage precursor populations in BXSB mice: possible reason for the increasing monocytosis in male mice. Clin Immunol Immunopathol 65(3):212-8 |
| abstractText | The BXSB mouse spontaneously develops an autoimmune disease that resembles human systemic lupus erythematosus (SLE). During their lifetime, male BXSB mice show an increasing monocytosis in the peripheral blood as opposed to their female littermates. This monocytosis is unique among autoimmune-prone mice. To test the hypothesis that alterations at the stem cell level may be responsible for this monocytosis, myeloid bone marrow precursor cells were examined in both male and female BXSB mice from 4 to 40 weeks of age. The number of M-CSF responding stem cells (CFU-M) and the number of GM-CSF responding stem cells (CFU-GM) were higher than in all other inbred mouse strains tested. In addition, male BXSB mice developed a progressive increase of CFU-M and CFU-GM in the bone marrow during their lifetime, which paralleled the peripheral blood monocytosis. The monocytosis in male BXSB mice is the result of a further expansion of the strain-specific high number of macrophage precursors by intrinsic factors, which may be attributed to the influence of the Yaa factor. The sex-specific expanded mononuclear phagocyte system may promote the autoimmune process and may be one reason for the dramatic course of murine SLE in male BXSB mice. |
