Developmental potential and dynamic behavior of hematopoietic stem cells

We have used retrovirus-mediated gene transfer to mark hematopoietic stem cells in vitro and have tracked the fate of these cells after their transplantation into lethally irradiated recipients. Several classes of stem cells are demonstrated, including cells whose progeny completely repopulate all hematopoietic lineages as well as cells that contribute predominantly to certain lineages or to specific anatomical locations. In a majority of recipients, we find that few (1 or 2) stem-cell clones account for the majority of the mature hematopoietic cells. These results coupled with retransplantation studies suggest an in vivo mechanism for the temporal control of stem-cell use. Further studies based on periodic sampling of primary recipients suggest that normal hematopoiesis results from the sequential activation of different stem-cell clones rather than from an averaged contribution of the entire stem-cell pool.

[1]  J. Till,et al.  A STOCHASTIC MODEL OF STEM CELL PROLIFERATION, BASED ON THE GROWTH OF SPLEEN COLONY-FORMING CELLS. , 1964, Proceedings of the National Academy of Sciences of the United States of America.

[2]  H. Micklem,et al.  Serial depletion and regeneration of the murine hematopoietic system. Implications for hematopoietic organization and the study of cellular aging , 1982, The Journal of experimental medicine.

[3]  J. Dick,et al.  Introduction of a selectable gene into primitive stem cells capable of long-term reconstitution of the hemopoietic system of W/Wv mice , 1985, Cell.

[4]  C. E. Ford,et al.  Interrelationships of myeloid and lymphoid cells: studies with chromosome-marked cells transfused into lethally irradiated mice , 1966, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[5]  G. Church,et al.  Genomic sequencing. , 1993, Methods in molecular biology.

[6]  K. Ozato,et al.  Hybridoma cell lines secreting monoclonal antibodies to mouse H-2 and Ia antigens. , 1980, Journal of immunology.

[7]  D. Raulet Expression and function of interleukin-2 receptors on immature thymocytes , 1985, Nature.

[8]  J. Sprent,et al.  A monoclonal antibody discriminating between subsets of T and B cells. , 1981, Journal of immunology.

[9]  E. Stanley,et al.  Methods for the purification, assay, characterization and target cell binding of a colony stimulating factor (CSF-1). , 1981, Journal of immunological methods.

[10]  Y. Kitamura,et al.  Spleen colony-forming cell as common precursor for tissue mast cells and granulocytes , 1981, Nature.

[11]  P. Tynan,et al.  Survival of mononuclear phagocytes depends on a lineage-specific growth factor that the differentiated cells selectively destroy , 1982, Cell.

[12]  E. Palmer,et al.  Y-encoded, species-specific DNA in mice: Evidence that the Y chromosome exists in two polymorphic forms in inbred strains , 1984, Cell.

[13]  G. Keller,et al.  Expression of a foreign gene in myeloid and lymphoid cells derived from multipotent haematopoietic precursors , 1985, Nature.

[14]  G. Zant Studies of hematopoietic stem cells spared by 5-fluorouracil. , 1984 .

[15]  K. A. Wall,et al.  Characterization of the Murine Antigenic Determinant, Designated L3T4a, Recognized by Monoclonal Antibody GK 1.5: Expression of L3T4a by Functional T Cell Clones Appears to Correlate Primarily with Class II MHC Antigen‐Reactivity , 1983, Immunological reviews.

[16]  D. Harrison,et al.  Loss of proliferative capacity in immunohemopoietic stem cells caused by serial transplantation rather than aging , 1978, The Journal of experimental medicine.

[17]  C. Cepko,et al.  Construction and applications of a highly transmissible murine retrovirus shuttle vector , 1984, Cell.

[18]  P Berg,et al.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. , 1977, Journal of molecular biology.

[19]  A. Glasebrook,et al.  IgG or IgM monoclonal antibodies reactive with different determinants on the molecular complex bearing Lyt 2 antigen block T cell-mediated cytolysis in the absence of complement. , 1980, Journal of immunology.

[20]  B. Mintz,et al.  Monoclonal derivation of mouse myeloid and lymphoid lineages from totipotent hematopoietic stem cells experimentally engrafted in fetal hosts. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[21]  J. Eliason,et al.  Isolation , 2024, Encyclopedia of Database Systems.

[22]  B. B. Mishell,et al.  Selected Methods in Cellular Immunology , 1980 .

[23]  G. Johnson,et al.  Monoclonal origin of B lymphocyte colony-forming cells in spleen colonies formed by multipotential hemopoietic stem cells , 1978, The Journal of experimental medicine.

[24]  H. Kay HOW MANY CELL-GENERATIONS? , 1965, Lancet.

[25]  D. Melton,et al.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. , 1984, Nucleic acids research.

[26]  Tatsutoshi Nakahata,et al.  A stochastic model of self‐renewal and commitment to differentiation of the primitive hemopoietic stem cells in culture , 1982, Journal of cellular physiology.

[27]  G. Hodgson,et al.  Properties of haematopoietic stem cells surviving 5-fluorouracil treatment: evidence for a pre-CFU-S cell? , 1979, Nature.

[28]  J. Till,et al.  CYTOLOGICAL EVIDENCE FOR A RELATIONSHIP BETWEEN NORMAL HEMATOPOIETIC COLONY-FORMING CELLS AND CELLS OF THE LYMPHOID SYSTEM , 1968, The Journal of experimental medicine.

[29]  David A. Williams,et al.  Introduction of new genetic material into pluripotent haematopoietic stem cells of the mouse , 1984, Nature.

[30]  K. Arai,et al.  A cloned MCGF cDNA encodes a multilineage hematopoietic growth factor: multiple activities of interleukin 3. , 1985, Journal of immunology.

[31]  W. Rutter,et al.  Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.

[32]  Rg Miller,et al.  The identification in adult bone marrow of pluripotent and restricted stem cells of the myeloid and lymphoid systems , 1977, The Journal of experimental medicine.

[33]  J. Loutit,et al.  Tissue grafting and radiation , 1967 .

[34]  A. Bernstein,et al.  RNA tumor viruses , 1982 .

[35]  D. Baltimore,et al.  Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus , 1983, Cell.

[36]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[37]  B. Vogelstein,et al.  Preparative and analytical purification of DNA from agarose. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[38]  D. Metcalf The hemopoietic colony stimulating factors , 1984 .

[39]  M. Moore,et al.  The fate of fetal and adult B-cell progenitors grafted into immunodeficient CBA/N mice , 1979, The Journal of experimental medicine.

[40]  P. Kantoff,et al.  Gene expression in mice after high efficiency retroviral-mediated gene transfer. , 1985, Science.

[41]  R. Schofield The relationship between the spleen colony-forming cell and the haemopoietic stem cell. , 1978, Blood cells.

[42]  J. Till,et al.  THE DISTRIBUTION OF COLONY-FORMING CELLS AMONG SPLEEN COLONIES. , 1963, Journal of cellular and comparative physiology.

[43]  L. Wysocki,et al.  "Panning" for lymphocytes: a method for cell selection. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[44]  L. Herzenberg,et al.  Properties of monoclonal antibodies to mouse Ig allotypes, H-2, and Ia antigens. , 1978, Current topics in microbiology and immunology.

[45]  U. Erikson,et al.  INTRAVENOUS UROGRAPHY IN HYPERTENSION , 1975, The Lancet.