Mock retroviral infection alters the developmental potential of murine bone marrow stem cells

Retroviral vectors were used to introduce an activated ras gene into murine pluripotent hemopoietic stem cells. We attempted to reconstitute the hemopoietic system of lethally irradiated mice with isolated spleen colonies obtained in vivo after injection of infected bone marrow cells. Spleen colonies derived from infected bone marrow were inefficient in promoting long-term survival of irradiated hosts. This loss of reconstitutive capacity of spleen colonies was not due to the retroviral infection per se but to the in vitro culture of spleen colony precursors. Incubation for 24 h in the presence of fetal calf serum and interleukin-3 without virus-producing cells was sufficient to abolish completely the reconstitutive capacity of spleen colonies while maintaining both self-renewal and pluripotential capacities of spleen colony precursors. These results show that the in vitro manipulation of stem cells that is included in current protocols for retroviral infection can modify the developmental potential of these cells. This finding clearly indicates that the use of retroviral vectors can introduce a bias in the analysis of hemopoiesis.

[1]  S. Karlsson,et al.  Expression of the human beta-globin gene following retroviral-mediated transfer into multipotential hematopoietic progenitors of mice. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[2]  I. Weissman,et al.  Purification and characterization of mouse hematopoietic stem cells. , 1988, Science.

[3]  I. Bertoncello,et al.  Multiparameter analysis of transplantable hemopoietic stem cells. II. Stem cells of long-term bone marrow-reconstituted recipients. , 1988, Experimental hematology.

[4]  G. Keller,et al.  Clonal fluctuation within the haematopoietic system of mice reconstituted with retrovirus‐infected stem cells. , 1987, The EMBO journal.

[5]  T. Hawley,et al.  Handicapped retroviral vectors efficiently transduce foreign genes into hematopoietic stem cells. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[6]  H. Micklem,et al.  Numbers and dispersion of repopulating hematopoietic cell clones in radiation chimeras as functions of injected cell dose. , 1987, Experimental hematology.

[7]  J. Visser,et al.  Separation and functional analysis of bone marrow cells separated by rhodamine-123 fluorescence. , 1987, Experimental hematology.

[8]  T. Inoue,et al.  Fraction of pluripotent hemopoietic stem cells in DNA synthesis varies with generation age. , 1986, Experimental hematology.

[9]  Ihor R. Lemischka,et al.  Developmental potential and dynamic behavior of hematopoietic stem cells , 1986, Cell.

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

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

[12]  I. Bertoncello,et al.  Multiparameter analysis of transplantable hemopoietic stem cells: I. The separation and enrichment of stem cells homing to marrow and spleen on the basis of rhodamine-123 fluorescence. , 1985, Experimental hematology.

[13]  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.

[14]  T. Dexter,et al.  Defective ability to self-renew in vitro of highly purified primitive haematopoietic cells , 1985, Nature.

[15]  Samuel Hellman,et al.  An in vitro clonal assay of adherent stem cells (ASC) in mouse marrow , 1984, Journal of cellular physiology.

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

[17]  Cori Bargmann,et al.  Human colon carcinoma Ki-ras2 oncogene and its corresponding proto-oncogene , 1984, Molecular and cellular biology.

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

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

[20]  M. Magli,et al.  Transient nature of early haematopoietic spleen colonies , 1982, Nature.

[21]  G. Hodgson,et al.  The organization of hemopoietic tissue as inferred from the effects of 5-fluorouracil. , 1982, Experimental hematology.

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

[23]  H. Koenig A stochastic model of stem cell proliferation, based on the growth of spleen colony-forming cells: , 1964 .

[24]  J. Till,et al.  A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. , 1961, Radiation research.