Abstract
The characterization of hepatic progenitor cells is of great scientific and clinical interest. Here we report that intravenous injection of adult bone marrow cells in the FAH−/− mouse, an animal model of tyrosinemia type I, rescued the mouse and restored the biochemical function of its liver. Moreover, within bone marrow, only rigorously purified hematopoietic stem cells gave rise to donor-derived hematopoietic and hepatic regeneration. This result seems to contradict the conventional assumptions of the germ layer origins of tissues such as the liver, and raises the question of whether the cells of the hematopoietic stem cell phenotype are pluripotent hematopoietic cells that retain the ability to transdifferentiate, or whether they are more primitive multipotent cells.
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References
Weissman, I.L. Translating stem and progenitor cell biology to the clinic: barriers and opportunities . Science 287, 1442–1446 (2000).
Till, J. & McCulloch, E. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat. Res. 14 (1961).
Wu, A., Till, J., Siminovitch, L. & McCulloch, E. Cytological evidence for a relationship between normal hematopoietic colony-forming cells and cells of the lymphoid system. J. Exp. Med. 127, 455–467 (1968).
Michalopoulos, G.K. & DeFrances, M.C. Liver regeneration . Science 276, 60–66 (1997).
Petersen, B.E. et al. Bone marrow as a potential source of hepatic oval cells. Science 284, 1168–1170 ( 1999).
Theise, N.D. et al. Derivation of hepatocytes from bone marrow cells in mice after radiation-induced myeloablation. Hepatology 31, 235–240 (2000).
Grompe, M. et al. Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice. Genes Dev. 7, 2298–2307 (1993).
Grompe, M. et al. Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I. Nature Genet. 10, 453–460 ( 1995).
Overturf, K. et al. Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I. Nature Genet. 12, 266–273 ( 1996); erratum: 12, 458.
Zambrowicz, B.P. et al. Disruption of overlapping transcripts in the ROSA beta geo 26 gene trap strain leads to widespread expression of β-galactosidase in mouse embryos and hematopoietic cells. Proc. Natl. Acad. Sci. USA 94, 3789–3794 ( 1997).
Morrison, S.J., Shah, N.M. & Anderson, D.J. Regulatory mechanisms in stem cell biology . Cell 88, 287–298 (1997).
Spangrude, G.J., Heimfeld, S. & Weissman, I.L. Purification and characterization of mouse hematopoietic stem cells. Science 241, 58–62 (1988).
Ikuta, K. & Weissman, I.L. Evidence that hematopoietic stem cells express mouse c-kit but do not depend on steel factor for their generation. Proc. Natl. Acad. Sci. USA 89, 1502–1506 (1992).
Uchida, N. & Weissman, I.L. Searching for hematopoietic stem cells: evidence that Thy-1.1lo Lin- Sca-1+ cells are the only stem cells in C57BL/Ka-Thy-1.1 bone marrow. J. Exp. Med. 175, 175–184 (1992).
Weissman, I.L. Stem cells, clonal progenitors, and commitment to the three lymphocyte lineages: T, B, and NK cells. Immunity 1, 529– 531 (1994).
Smith, L.G., Weissman, I.L. & Heimfeld, S. Clonal analysis of hematopoietic stem-cell differentiation in vivo. Proc. Natl. Acad. Sci. USA 88, 2788–2792 (1991).
Morrison, S.J., Wandycz, A.M., Hemmati, H.D., Wright, D.E. & Weissman, I.L. Identification of a lineage of multipotent hematopoietic progenitors. Development 124, 1929–1939 ( 1997).
Uchida, N. Characterization of mouse hematopoietic stem cells. Ph.D. thesis, Stanford University, Stanford, California 152–213 (1992).
van Ewijk, W., van Soest, P.L. & van den Engh, G.J. Fluorescence analysis and anatomic distribution of mouse T lymphocyte subsets defined by monoclonal antibodies to the antigens Thy-1, Lyt-1, Lyt-2, and T-200. J. Immunol. 127, 2594–2604 ( 1981).
Ledbetter, J.A. & Herzenberg, L.A. Xenogeneic monoclonal antibodies to mouse lymphoid differentiation antigens. Immunol. Rev. 47, 63–90 (1979).
Shizuru, J.A., Jerabek, L., Edwards, C.T. & Weissman, I.L. Transplantation of purified hematopoietic stem cells: requirements for overcoming the barriers of allogeneic engraftment. Biol. Blood Marrow Transplant. 2, 3–14 (1996 ); erratum: 3, 50.
Talbot, N.C. et al. Colony isolation and secondary culture of fetal porcine hepatocytes on STO feeder cells. In Vitro Cell Dev. Biol. Anim. 30A, 851–858 (1994).
Overturf, K., al-Dhalimy, M., Ou, C.N., Finegold, M. & Grompe, M. Serial transplantation reveals the stem-cell-like regenerative potential of adult mouse hepatocytes. Am. J. Pathol. 151, 1273–1280 (1997).
Braun, K.M., Degen, J.L. & Sandgren, E.P. Hepatocyte transplantation in a model of toxin-induced liver disease: Variable therapeutic effect during replacement of damaged parenchyma by donor cells. Nature Med. 6, 320– 326 (2000).
Uchida, N. et al. Hydroxyurea can be used to increase mouse c-kit+Thy-1. 1(lo)Lin-/loSca- 1(+) hematopoietic cell number and frequency in cell cycle in vivo. Blood 90, 4354–4362 ( 1997).
Taniguchi, H., Toyoshima, T., Fukao, K. & Nakauchi, H. Presence of hematopoietic stem cells in the adult liver. Nature Med. 2, 198–203 ( 1996).
Ferrari, G. et al. Muscle regeneration by bone marrow-derived myogenic progenitors . Science 279, 1528–1530 (1998); erratum, 281, 923.
Gussoni, E. et al. Dystrophin expression in the mdx mouse restored by stem cell transplantation. Nature 401, 390– 394 (1999).
Kopen, G.C., Prockop, D.J. & Phinney, D.G. Marrow stromal cells migrate throughout forebrain and cerebellum, and they differentiate into astrocytes after injection into neonatal mouse brains. Proc. Natl. Acad. Sci. USA 96 , 10711–10716 (1999).
Pereira, R.F. et al. Cultured adherent cells from marrow can serve as long-lasting precursor cells for bone, cartilage, and lung in irradiated mice. Proc. Natl. Acad. Sci. USA 92, 4857– 4861 (1995).
Weissman, I.L. Stem cells: units of development, units of regeneration, and units in evolution . Cell 100, 157–168 (2000).
Bjornson, C.R., Rietze, R.L., Reynolds, B.A., Magli, M.C. & Vescovi, A.L. Turning brain into blood: a hematopoietic fate adopted by adult neural stem cells in vivo. Science 283, 534– 537 (1999).
Jackson, K.A., Mi, T. & Goodell, M.A. Hematopoietic potential of stem cells isolated from murine skeletal muscle. Proc. Natl. Acad. Sci. USA 96, 14482–14486 (1999).
Sell, S. & Ilic, Z. in Liver Stem Cells (Landes, Austin, Texas, USA) Chapman and Hall, New York, New York, 29 –63 (1997).
Theise, N.D. et al. Liver from bone marrow in humans. Hepatology 32, 11–16 (2000).
Alison, M.R. et al. Hepatocytes from non-hepatic adult stem cells. Nature 406, 257 (2000).
Baum, C.M., Weissman, I.L., Tsukamoto, A.S., Buckle, A.M. & Peault, B. Isolation of a candidate human hematopoietic stem-cell population. Proc. Natl. Acad. Sci. USA 89, 2804–2808 ( 1992).
Overturf, K., Al-Dhalimy, M., Finegold, M. & Grompe, M. The repopulation potential of hepatocyte populations differing in size and prior mitotic expansion. Am. J. Pathol. 155, 2135–2143 (1999).
Strom, S.C., Chowdhury, J.R. & Fox, I.J. Hepatocyte transplantation for the treatment of human disease. Semin. Liver Dis. 19, 39– 48 (1999).
Ritt, A. National Bone Marrow Donor Registry to begin recruiting in general population this summer. J. Am. Med. Assoc. 259, 3099 –3101 (1988).
Murata, M. et al. Unrelated bone marrow transplantation from the National Marrow Donor Program. Int. J. Hematol. 66, 239– 243 (1997).
Carella, A.M., Champlin, R., Slavin, S., McSweeney, P. & Storb, R. Mini-allografts: ongoing trials in humans. Bone Marrow Transplant. 25, 345–350 (2000).
Hale, D.A., Gottschalk, R., Umemura, A., Maki, T. & Monaco, A.P. Establishment of stable multilineage hematopoietic chimerism and donor-specific tolerance without irradiation. Transplantation 69, 1242–1251 (2000).
Nolan, G.P., Fiering, S., Nicolas, J.F. & Herzenberg, L.A. Fluorescence-activated cell analysis and sorting of viable mammalian cells based on beta-D-galactosidase activity after transduction of Escherichia coli lacZ. Proc. Natl. Acad. Sci. USA 85, 2603–2607 (1988).
MacGregor, G.R., Mogg, A.E., Burke, J.F. & Caskey, C.T. Histochemical staining of clonal mammalian cell lines expressing E. coli beta galactosidase indicates heterogeneous expression of the bacterial gene. Somat. Cell Mol. Genet. 13, 253–265 (1987).
Acknowledgements
We thank L. Jerabek for help with the mice, A. Tsukamoto for review of the manuscript, M. Masek for optimizing staining protocols and M. Ferraz for animal care. This work was supported in part by the National Institutes of Health (I.L.W and M.G.) and the American Liver Foundation (X.W).
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Lagasse, E., Connors, H., Al-Dhalimy, M. et al. Purified hematopoietic stem cells can differentiate into hepatocytes in vivo. Nat Med 6, 1229–1234 (2000). https://doi.org/10.1038/81326
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DOI: https://doi.org/10.1038/81326
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