Skip to main content
Log in

Identification and purification of human erythroid progenitor cells by monoclonal antibody to the transferrin receptor (TÜ 67)

  • Original Articles
  • Published:
Blut Aims and scope Submit manuscript

Summary

Anti-TÜ 67 is a murine monoclonal antibody that recognizes the transferrin receptor. With respect to hematopoietic cells TÜ 67 is expressed by human multipotent colony-forming cells (CFU-Mix), erythroid progenitor cells (BFU-E and CFU-E) and a fraction of granulocyte/monocyte colony forming cells, but is not expressed by mature hematopoietic cells including erythrocytes, platelets, lymphocytes, and peripheral blood myeloid cells. The TÜ 67-positive fraction of normal bone marrow, separated by fluorescence-activated cell sorting (FACS) or immune rosettes, contained 87% of the erythroid progenitor cells. Erythroid progenitor cells were enriched up to 50-fold by using a combination of monoclonal antibodies to deplete mature hematopoietic cells, followed by positive selection of BFU-E and CFU-E by TÜ 67 antibody.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Beverly PCL, Linch D, Delia D (1980) Isolation of human haematopoietic progenitor cells using monoclonal antibodies. Nature 287: 332–333

    Google Scholar 

  2. Bodger MP, Izaguirre CA, Blacklock HA, Hoffbrand AV (1983) Surface antigen determinants on human pluripotent and unipotent hematopoietic progenitor cells. Blood 61: 1006–1010

    Google Scholar 

  3. Civin CI, Strauss LC, Brovall C, Fackler MJ, Schwartz JF, Shaper JH (1984) Antigenic analysis of hematopoiesis; a hematopoietic progenitor cell surface antigen defined by a monoclonal antibody raised against KG-1 a cells. J Immunol 133: 157–165

    Google Scholar 

  4. Dipersio JF, Brennan JK, Lichtman MA, Speiser BL (1978) Human cell lines that elaborate colony-stimulating activity for the marrow cells of man and other species. Blood 51: 507–519

    Google Scholar 

  5. Fauser AA, Messner HA (1978) Granuloerythropoietic colonies in human bone marrow, peripheral blood, and cord blood. Blood 52: 1243–1248

    Google Scholar 

  6. Greenberg PL, Baker S, Link M, Minowada J (1985) Immunologic selection of hemopoietic precursor cells utilizing antibody-mediated plate binding (“panning”). Blood 65: 190–197

    Google Scholar 

  7. Griffin JD, Ritz J, Nadler LM, Schlossman SF (1981) Expression of myeloid differentiation antigens on normal and malignant cells. J Clin Invest 68: 932–941

    Google Scholar 

  8. Griffin JD, Beveridge RP, Schlossman SF (1982) Isolation of myeloid progenitor cells from peripheral blood of chronic myelogenous leukemia patients. Blood 60: 30–37

    Google Scholar 

  9. Griffin JD, Larcom P, Schlossman SF (1983) Use of surface markers to identify a subset of acute myelomonocytic leukemia cells with progenitor cell properties. Blood 62: 1300–1303

    Google Scholar 

  10. Griffin JD, Hercend T, Beveridge R, Schlossman SF (1983) Characterization of an antigen expressed by human natural killer cells. J Immunol 130: 2947–2951

    Google Scholar 

  11. Griffin JD, Linch D, Sabbath K, Schlossman SF (1984) A monoclonal antibody reactive with normal and leukemic human myeloid progenitor cells. Leuk Res 4: 521–531

    Google Scholar 

  12. Griffin JD, Sabbath KD, Larcom P, Herrmann F, Nichols K, Kornacki M, Levine H, Cannistra SA (1985) Differential expression HLA-DR antigens in subsets of human CFU-GM. Blood 66: 788–795

    Google Scholar 

  13. Hoang T, Gilmore D, Metcalf D, Cobbold S, Watt S, Clark M, Furth M, Waldmann H (1983) Separation of hemopoietic cells from adult mouse marrow by use of monoclonal antibodies. Blood 61: 580–588

    Google Scholar 

  14. Moore MAS, Williams N, Metcalf D (1973) In vitro colony formation by normal and leukemic human hematopoietic cells: Characterization of the colony-forming cells. J Natl Cancer Inst 50: 303–319

    Google Scholar 

  15. Nadler LM, Anderson KC, Marti G, Bates M, Park E, Daley JF, Schlossman SF (1983) B4, a human B lymphocyte-associated antigen expressed on normal mitogen-activated and malignant B lymphocytes. J Immunol 131: 244–250

    Google Scholar 

  16. Nicola NA, Metcalf D, von Mechner H, Burgess AW (1981) Isolation of murine fetal hemopoietic progenitor cells and selective fractionation of various erythroid precursors. Blood 58: 376–386

    Google Scholar 

  17. Papayannopoulou T, Brice M, Yokochi T, Rabinovitch PS, Lindsley D, Stamatoyannopolous G (1984) Anti-HEL cell monoclonal antibodies recognize determinants that are also present in hemopoietic progenitors. Blood 63: 326–334

    Google Scholar 

  18. Peng R, Al-Katib A, Knowles DM, Lu L, Broxmeyer H, Tolidjian B, Chiao R-W, Koziner B, Wang C-Y (1984) Preparation and characterization of monoclonal antibodies recognizing two distinct differentiation antigens (Pro-Im 1, Pro Im-2) on early hematopoietic cells. Blood 64: 1169–1178

    Google Scholar 

  19. Pike BI, Robinson WA (1970) Human bone marrow colony growth in agar gel. J Cell Physiol 76: 77–84

    Google Scholar 

  20. Reinherz EL, Schlossman SF (1984) Strategies for regulating the human immune response by selective T cell subset manipulation. In: Pfeffer A., (ed), The Potential role of the T Cell Population in Cancer Therapy. Raven, New York, pp 271–279

    Google Scholar 

  21. Reinherz EL, Kung PC, Goldstein G, Levey RH, Schlossman SF (1980) Discrete stages of human intrathymic differentiation: Analysis of normal thymocytes and leukemic lymphoblasts of T lineage. Proc Natl Acad Sci USA 77: 1588–1592

    Google Scholar 

  22. Ritz J, Pesando JM, Notis-McConarty J, Lazarus H, Schlossman SF (1980) A monoclonal antibody to human acute lymphoblastic leukemia antigen. Nature 283: 583–585

    Google Scholar 

  23. Robinson J, Sieff C, Delia D, Edwards PAW, Greaves MF (1981) Expression of cell surface HLA-DR, HLA-ABC and glycophorin during erythroid differentiation. Nature 289: 68–71

    Google Scholar 

  24. Sabbath KD, Ball ED, Larcom P, Davis R, Griffin JD (1985) Heterogeneity of clonogenic cells in acute myeloblastic leukemia. J Clin Invest 75: 746–753

    Google Scholar 

  25. Stashenko P, Nadler LM, Hardy R, Schlossman SF (1980) Characterization of a human B lymphocyte specific antigen. J Immunol 125: 1678–1685

    Google Scholar 

  26. Todd RF, Nadler LM, Schlossman SF (1981) Antigens on human monocytes identified by monoclonal antibodies. J Immunol 126: 1435–1442

    Google Scholar 

  27. Todd RF, Meuer SC, Romain PL, Schlossmann SF (1984) A monoclonal antibody that blocks class II histocompatibiliy-related immune interactions. Hum Immunol 10: 23–34

    Google Scholar 

  28. Uchanska-Ziegler B, Wernet P, Liangru S, Ziegler A (1984) Do monoclonal antibodies TÜ 15 and TÜ 16 detect heterogeneity of human transferrin receptor molecules? Fed Eur Biochem Soc 175: 279–2951

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by the Deutsche Forschungsgemeinschaft (He 1380-2/1)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Herrmann, F., Griffin, J.D., Sabbath, K.D. et al. Identification and purification of human erythroid progenitor cells by monoclonal antibody to the transferrin receptor (TÜ 67). Blut 56, 179–183 (1988). https://doi.org/10.1007/BF00320749

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00320749

Key words

Navigation