Diamond-blackfan anemia: in vitro response of erythroid progenitors to the ligand for c-kit.

To provide insights into the pathogenesis of Diamond-Blackfan anemia, we examined the in vitro response of erythroid progenitors to the recently isolated ligand for c-kit (stem cell factor, SCF). For these studies, marrow or blood mononuclear cells from 10 Diamond-Blackfan patients were cultured with erythropoietin (Ep), Ep and interleukin-3, Ep and granulocyte-macrophage colony-stimulating factor, or Ep and lymphocyte conditioned media (LCM). These combinations were tested in the presence or absence of SCF. The mean number of cells per erythroid burst increased 5 to 50-fold in cultures containing SCF. Furthermore, many additional erythroid bursts were seen (mean increment 3.2 x baseline values). Although burst-forming unit-erythroid (BFU-E) from all patients responded, there were differences among individuals in the sensitivity of their BFU-E to SCF. In six patients and all control studies, plateau frequencies of erythroid bursts were achieved with less than or equal to 10 ng/mL SCF, whereas in studies from the other four patients, over 50 ng/mL SCF was required. These data invite speculation that the c-kit receptor/ligand axis is involved in the pathogenesis of Diamond-Blackfan anemia. More importantly and regardless of whether the observed patterns of response reflect the primary defect or an epiphenomenon, our data strongly support a therapeutic trial of SCF in patients with Diamond-Blackfan anemia.

[1]  P. Leder,et al.  Transmembrane form of the kit ligand growth factor is determined by alternative splicing and is missing in the SId mutant , 1991, Cell.

[2]  P. Leder,et al.  The hematopoietic growth factor KL is encoded by the SI locus and is the ligand of the c-kit receptor, the gene product of the W locus , 1990, Cell.

[3]  David A. Williams,et al.  Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor , 1990, Cell.

[4]  C. March,et al.  Identification of a ligand for the c-kit proto-oncogene , 1990, Cell.

[5]  K. Zsebo,et al.  Primary structure and functional expression of rat and human stem cell factor DNAs , 1990, Cell.

[6]  K. Nocka,et al.  Candidate ligand for the c‐kit transmembrane kinase receptor: KL, a fibroblast derived growth factor stimulates mast cells and erythroid progenitors. , 1990, The EMBO journal.

[7]  K. Nocka,et al.  Molecular bases of dominant negative and loss of function mutations at the murine c‐kit/white spotting locus: W37, Wv, W41 and W. , 1990, The EMBO journal.

[8]  A. Reith,et al.  W mutant mice with mild or severe developmental defects contain distinct point mutations in the kinase domain of the c-kit receptor. , 1990, Genes & development.

[9]  J. Carey,et al.  Congenital hypoplastic (Diamond-Blackfan) anemia in seven members of one kindred. , 1990, American journal of medical genetics.

[10]  J. Lipton,et al.  An intrinsic progenitor defect in Diamond‐Blackfan anaemia , 1989, British journal of haematology.

[11]  Z. Estrov,et al.  Diamond-Blackfan anemia: promotion of marrow erythropoiesis in vitro by recombinant interleukin-3. , 1989, Blood.

[12]  D. Halperin,et al.  Diamond-blackfan anemia: etiology, pathophysiology, and treatment. , 1989, The American journal of pediatric hematology/oncology.

[13]  E. Guinan,et al.  Bone marrow transplantation for constitutional pure red cell aplasia. , 1988, Blood.

[14]  J. Adamson,et al.  Pure red cell aplasia: Response to therapy with anti‐thymocyte globulin , 1986, American journal of hematology.

[15]  J. Lipton,et al.  Defective erythroid progenitor differentiation system in congenital hypoplastic (Diamond-Blackfan) anemia. , 1986, Blood.

[16]  M. Freedman,et al.  Diamond-Blackfan Syndrome. II. In Vitro Corticosteroid Effect on Erythropoiesis , 1982, Pediatric Research.

[17]  J. Finlay,et al.  Bone-marrow microenvironment defect in congenital hypoplastic anemia. , 1980, The New England journal of medicine.

[18]  E. Russell Hereditary anemias of the mouse: a review for geneticists. , 1979, Advances in genetics.

[19]  D. Housman,et al.  Erythroid precursors in congenital hypoplastic (Diamond-Blackfan) anemia. , 1978, The Journal of clinical investigation.

[20]  R. Hoffman,et al.  Diamond-Blackfan syndrome: lymphocyte-mediated suppression of erythropoiesis. , 1976, Science.

[21]  J. Till,et al.  The cellular basis of the genetically determined hemopoietic defect in anemic mice of genotype Sl-Sld. , 1965, Blood.

[22]  J. Till,et al.  Spleen-Colony Formation in Anemic Mice of Genotype WW , 1964, Science.

[23]  Diamond Lk,et al.  CONGENITAL hypoplastic anemia. , 1957, Nutrition reviews.