Abstract
Cells of the murine hemopoietic cell line FDC-P1 were multiply infected with a retroviral construct containing cDNA encoding the leukemia inhibitory factor (LIF) to produce cells secreting high levels of LIF. Injection of these cells to unirradiated or irradiated syngeneic DBA/2 mice resulted in animals engrafted with LIF-producing cells in the marrow, spleen, and lymph nodes and with elevated serum LIF levels. These mice developed within 12-70 days a fatal syndrome characterized by cachexia, excess new bone formation, calcification in heart and skeletal muscle, pancreatitis, thymus atrophy, and abnormalities in the adrenal cortex and ovarian corpora lutea. Injection of mice with control FDC-P1 cells led to comparable organ engraftment, but the mice developed none of these lesions. The observations suggest that LIF may be a potent cachexia-inducing agent and may have marked effects on osteoblasts and calcium metabolism.
MeSH Terms
Animals
Bone Marrow/pathology
Bone and Bones/pathology
Cell Line
Female
Growth Inhibitors/biosynthesis,genetics,toxicity
Hematopoietic Stem Cell Transplantation
Hematopoietic Stem Cells/metabolism
Interleukin-6
Leukemia Inhibitory Factor
Lymphokines
Mice
Mice, Inbred DBA
Ovary/pathology
Pancreas/pathology
Syndrome
Transcription, Genetic
Weight Loss
Chemicals
Growth Inhibitors
Interleukin-6
Leukemia Inhibitory Factor
Lif protein, mouse
Lymphokines
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Metcalf D
The Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
Gearing D P
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