The first-appearance of neutrophils in the human fetal bone marrow cavity

Early Human Development

Volumn 53, Issue 2, 1998, Pages 129-144

  Slayton, William B ^a   Li, Yan ^a   Calhoun, Darlene A ^a   Juul, Sandra E ^a   Iturraspe, Jose ^a   Braylan, Raul C ^a   Christensen, Robert D ^a  

^a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

Author keywords

Development; Fetus; Granulocyte colony stimulating factor; Neutrophil; PCR

Indexed keywords

CD11B ANTIGEN; CD15 ANTIGEN; CELL SURFACE RECEPTOR; GRANULOCYTE COLONY STIMULATING FACTOR; MESSENGER RNA; MONOCLONAL ANTIBODY; MYELOPEROXIDASE;

ARTICLE; BONE DEVELOPMENT; BONE MARROW; CLAVICLE; FETUS; FIRST TRIMESTER PREGNANCY; FLOW CYTOMETRY; HUMAN; IMMUNOHISTOCHEMISTRY; NEUTROPHIL; NORMAL HUMAN; POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION;

ANTIGENS, CD11; ANTIGENS, CD15; BONE MARROW; BONE MARROW CELLS; ERYTHROCYTE COUNT; FEMALE; GESTATIONAL AGE; GRANULOCYTE COLONY-STIMULATING FACTOR; HEMATOPOIESIS; HUMANS; IMMUNOHISTOCHEMISTRY; LEUKOCYTE COUNT; NEUTROPHILS; PREGNANCY; RECEPTORS, GRANULOCYTE COLONY-STIMULATING FACTOR; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, MESSENGER;

EID: 0032401774     PISSN: 03783782     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-3782(98)00049-8     Document Type: Article

References (37)

1. Charboard P., Tavian M., Humeau L., Peault B. Early ontogeny of the human marrow from long bones: an immunohistochemical study of hematopoiesis and its micro-environment. Blood. 78:1996;4109-4119.
2. Keleman E, Calvo W, Fliedner TM. Atlas of human hemopoietic development. New York: Springer-Verlag, 1979.
3. Dimetri G., Griffin J. Granulocyte colony stimulating factor and its receptor. Blood. 78:1991;2791-2808.
4. Lieschke G., Grail D., Hodgson G.et al. Mice lacking granulocyte colony-stimulating factor have chronic neutropenia, granulocyte, and macrophage progenitor cell deficiency, and impaired neutrophil mobilization. Blood. 84:1994;1737-1746.
5. Hern W. Correlation of fetal age and measurements between 10 and 26 weeks gestation. Obstet. Gynecol. 63:1984;26-32.
6. Keleman E., Janossa M., Calvo W., Fliedner T.M. Developmental age estimated by bone-length measurement in human fetuses. Anat. Rec. 209:1984;547-552.
7. Buccheri V., Shetty V., Yoshida N., Morilla R., Matutes E., Catovsky D. The role of an anti-myeloperoxidase antibody in the diagnosis and classification of acute leukaemia, a comparison with light and electron microscopy. Br. J. Haematol. 80:1992;62-68.
8. McCracken S., Layton J.E., Shorter S.C., Starkey P.M., Barlow D.H., Mardon H.J. Expression of granulocyte-colony stimulating factor and its receptor is regulated during the development of the human placenta. J. Endocrinol. 149:1996;249-258.
9. Saito S., Ichijo N.S. Expression of granulocyte colony-stimulating factor and its receptor at the feto-maternal interface in murine and human pregnancy. Growth Factors. 10:1994;135-143.
10. Wetzstein M, Volker U, Dedio J, Lobau S, Zuber U, Schiesswohl M, Hergert C, Hecker M, Schumann W. Cloning, sequencing and molecular analysis of the danK locus from Bacillus subtilis. J Bacteriol 1992;174:3300-10.
11. Nagata S., Tsuchiya M., Asano S.et al. The chromosomal gene structure and two mRNAs for human granulocyte colony-stimulating factor. EMBO J. 5:1986;575-581.
12. Fukunaga R., Seto Y., Mizushima S., Nagata S. Three different mRNA's encoding human granulocyte colony-stimulating factor. Proc. Natl. Acad. Sci. U.S.A. 87:1990;8702-8706.
13. Nakajima-Iijima S., Hamada H., Reddy P., Kakunaga T. Molecular structure of the human cytoplasmic β-Actin gene: interspecies homology of sequences in the introns. Proc. Natl. Acad. Sci. U.S.A. 82:1985;6133-6137.
14. Slayton W.B., Juul S.E., Calhoun D.A., Li Y., Braylan R.D., Christensen R.D. Hematopoiesis in the liver and marrow of human fetuses at 5 and 16 weeks postconception: Quantitative assessment of macrophage and neutrophil populations. Pediatr Res. 43:1988;774-782.
15. Terstappen L.W., Safford M., Loken M.R. Flow cytometric analysis of human bone marrow III. Neutrophil maturation. Leukemia. 4:1990;657-663.
16. Cairo M. Therapeutic implications for dysregulated colony-stimulating factor expression in neonates. Blood. 82:1993;2269-2272.
17. Hill H. Biochemical, structural, and functional abnormalities of polymorphonuclear leukocytes in the neonate. Pediatr. Res. 22:1987;375-380.
18. Wilson C. Immunologic basis for increased susceptibility of the neonate to infection. J. Pediatr. 108:1986;1-12.
19. Erdman S., Christensen R.D., Bradley P., Rothstein G. Supply and release of storage neutrophils: a developmental study. Biol. Neonate. 41:1982;132-137.
20. Zeligs B., Armstrong C., Walser J., Bellanti J. Age-dependant susceptibility of neonatal rats to group B streptococcal type III infection: correlation of severity of infection and response of myeloid pools. Infect. Immunol. 37:1982;255-263.
21. Christensen R.D., Rothstein G. Exhaustion of the mature marrow neutrophils in neonates with sepsis. J. Pediatr. 96:1980;316-318.
22. Christensen R.D., Bradley R., Rothstein G. The leukocyte left shift in clinical and experimental neonatal sepsis. J. Pediatr. 98:1981;101-105.
23. Liechty K., Schibler K., Ohls R., Pekins S., Christensen R. The failure of newborn mice infected with Escherichia coli to accelerate neutrophil production correlates with their failure to increase transcripts for granulocyte-colony-stimulating factor and interleukin-6. Biol. Neonate. 64:1993;331-340.
24. Cairo M., Worcester C., Ruker R.et al. Randomized trial of granulocyte transfusions versus intravenous immune globulin therapy for neonatal neutropenia and sepsis. J. Pediatr. 120:1992;281-285.
25. Wheeler J. Neutrophil storage pool depletion in septic, neutropenic neonates. Pediatr. Infect. Dis. J. 33:1984;407-409.
26. Clark S.C., Kamen R. The human hematopoietic colony-stimulating factors. Science. 236:1987;1229-1237.
27. Liu F., Wu H.Y., Link D.C. Multiple cytokines appear to contribute to granulopoiesis in G-CSF receptor deficient mice. Blood. 88:1996;660a.
28. McClanahan T., Dalrymple S., Barkett M., Lee F. Hematopoietic growth factor receptor genes as markers of lineage commitment during in vitro development of hematopoietic cells. Blood. 81:1993;2903-2915.
29. Kittler E., McGrath H., Temeles D., Crittenden R., Kister V., Quesenberry P. Biologic significance of constitutive and subliminal growth factor production by bone marrow stroma. Blood. 79:1992;3168-3178.
30. Fibbe W., van Damme J., Billiau A.et al. Interleukin 1 induces human marrow stromal cells in long-term culture to produce granulocyte colony-stimulating factor. Blood. 71:1988;430-435.
31. Taichman R., Emerson S. Human osteosarcoma cell lines MG-63 and SaOS-2 produce G-CSF and GM-CSF: identification and partial characterization of cell-associated isoforms. Exp. Hematol. 24:1996;509-517.
32. Thacker J., Dedhar S., Hogge D. The effect of GM-CSF and G-CSF on the growth of human osteosarcoma cells in vitro and in vivo. Int. J. Cancer. 56:1994;236-243.
33. Wiktor-Jedrzejczak W., Bartocci W., Ferrante A. Total absence of colony-stimulating factor 1 in the macrophage deficient osteopetrotic (op/op) mouse. Proc. Natl. Acad. Sci. U.S.A. 87:1990;4828-4832.
34. Purton L., Lee M., Torok-Storb B. Normal human peripheral blood mononuclear cells mobilized with granulocyte colony-stimulating factor have increased osteoclastogenic potential compared to nonmobilized blood. Blood. 87:1996;1802-1808.
35. x-dependent and independent recognition pathways. Blood. 82:1993;182-191.
36. Smith J., Tabsh K. Fetal neutrophils and eosinophils express normal levels of L-selectin. Pediatr. Res. 34:1993;253-257.
37. Petrequin P.R., Todd R.F., Devall L.J., Boxer L.A., Curnutte J.T. Association between gelatinase release and increased plasma membrane expression of the Mo1 glycoprotein. Blood. 69:1987;605-610.