Anomalous plasma concentrations and impaired secretion of growth factors in fanconi's anemia
Autor: | F. Schilling, Ph. Hénon, E. Wunder, B. Thing Mortensen |
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Rok vydání: | 1996 |
Předmět: |
Adult
Male medicine.medical_specialty Stromal cell Adolescent Anemia Stem cell factor Biology Hematopoietic Cell Growth Factors Monocytes Pathogenesis Internal medicine medicine Humans Child Interleukin 6 Cells Cultured Stem Cell Factor Interleukin-6 Macrophages Granulocyte-Macrophage Colony-Stimulating Factor Cell Biology medicine.disease Colony-stimulating factor Pancytopenia Fanconi Anemia Phenotype Endocrinology Immunology biology.protein Molecular Medicine Female Stem cell Interleukin-1 Developmental Biology |
Zdroj: | STEM CELLS. 11:144-149 |
ISSN: | 1549-4918 1066-5099 |
Popis: | In Fanconi's anemia, which is known to be an autosomal recessive Mendelian trait with four complementary groups. In addition to stunning phenotypic variation at clinical and cellular levels, aplastic pancytopenia is a common feature. Since either an early block of differentiation in stem cells or their insufficient support by stromal functions could be an underlying factor, levels of stem cell factor (SCF) and cytokines have been measured in blood and in supernatants of monocytes after stimulation with granulocyte-macrophage colony stimulating factor (GM-CSF). In two of three FA patients, no GM-CSF was detectable, and simultaneously SCF was decreased to 8% and 15% of normal values. The combination of low SCF and GM-CSF may be implied in the pathogenesis of marrow aplasia, since comparison with W/Sl mice shows that impairment of the SCF/c-kit function alone has different effects. Also, this explains that treatment with GM-CSF in a recent study enhanced only leukogenesis and not all three lineages. In the third patient, both factors were normal, and here a different mechanism may act. In all three FA patients, interleukin 6 (IL-6) production in stimulated monocytes was decreased, which may hamper immune defense of infections in a nonspecific way. |
Databáze: | OpenAIRE |
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