Enhanced hematopoietic growth factor production in an experimental myeloproliferative syndrome.

Abstract

The murine myeloproliferative syndrome induced by the myeloproliferative sarcoma virus (MPSV) has numerous similarities to human primary myelofibrosis. We have shown that medium conditioned by spleen cells of MPSV-infected mice has the capacity to support the growth of primitive blast cell colonies. The detection of this activity associated with MPSV infection stimulated us to characterize the hematopoietins responsible for this activity. Northern blot analysis showed a large increase, or induction, of interleukin-6 (IL-6), granulocyte-macrophage colony-stimulating factor (GM-CSF), macrophage-CSF (CSF-1), and granulocyte-CSF (G-CSF) transcripts in the hematopoietic organs of MPSV-infected mice; however, no IL-3 transcript could be detected in either MPSV-infected or normal mice. Significant levels of IL-1 alpha, IL-6, G-CSF, and CSF-1 bioactivities were found in the serum of MPSV-infected mice, but not in controls. Additionally, analysis of medium conditioned by spleen cells of MPSV-infected mice showed the presence of tumor necrosis factor alpha bioactivity. The increased production of cytokines that are able to stimulate pluripotent hematopoietic stem cells corroborates the hypothesis of a possible involvement of hematopoietic growth factors in the development of some myeloproliferative disorders.

• Authors: M C Le Bousse-Kerdilès, M Souyri, F Smadja-Joffe, V Praloran, C Jasmin, H J Ziltener
• Journal: Blood (Blood) Vol. 79 Issue 12 Pg. 3179-87 (Jun 15 1992) ISSN: 0006-4971 [Print] United States
• PMID: 1375844 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Hematopoietic Cell Growth Factors
• Interleukin-6
• RNA, Messenger
• Tumor Necrosis Factor-alpha
• Granulocyte Colony-Stimulating Factor
• Macrophage Colony-Stimulating Factor

Topics

• Animals
• Blotting, Northern
• Cells, Cultured
• Gene Expression
• Granulocyte Colony-Stimulating Factor (biosynthesis, genetics)
• Hematopoietic Cell Growth Factors (biosynthesis, genetics)
• Interleukin-6 (biosynthesis, genetics)
• Liver (metabolism)
• Macrophage Colony-Stimulating Factor (biosynthesis, genetics)
• Male
• Mice
• Mice, Inbred DBA
• Myeloproliferative Disorders (metabolism, microbiology, pathology)
• RNA, Messenger (analysis, metabolism)
• Retroviridae Infections
• Spleen (metabolism, pathology)
• Thymus Gland (metabolism)
• Transcription, Genetic
• Tumor Necrosis Factor-alpha (analysis)