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Stem Cells 2004;22:334-343 www.StemCells.com
© 2004 AlphaMed Press

CDCP1 Identifies a Broad Spectrum of Normal and Malignant Stem/Progenitor Cell Subsets of Hematopoietic and Nonhematopoietic Origin

Hans-Jörg Bühringa, Selim Kuçib, Tim Conzea, Gisa Rathkea, Kerol Bartolovica, Frank Grünebacha, Marwa Scherl-Mostageerc, Tim H. Brümmendorfa, Norbert Schweiferc, Reiner Lammersd

a University of Tübingen, Department of Internal Medicine II, Division of Hematology, Immunology, Oncology and Rheumatology, Tübingen, Germany;
b University Children’s Hospital, Department of Hematology/Oncology, Tübingen, Germany;
c Boehringer Ingelheim Austria, Department of Exploratory Research, Research and Development, Vienna, Austria;
d University of Tübingen, Department of Internal Medicine IV, Division of Diabetes Research, Tübingen, Germany

Key Words. Stem cell marker • Phenotype • CDCP1

Hans-Jörg Bühring, Ph.D., Medizinische Klinik II, Otfried-Müller-Str.10, 72076 Tübingen, Germany. Telephone: 49-7071-2982730; Fax: 49-7071-292730; e-mail: hans-joerg.buehring{at}med.uni-tuebingen.de

CUB-domain-containing protein 1 (CDCP1) is a novel transmembrane molecule that is expressed in metastatic colon and breast tumors as well as on the surface of hematopoietic stem cells. In this study, we used multiparameter flow cytometry and antibodies against CDCP1 to analyze the expression of CDCP1 on defined hematopoietic cell subsets of different sources. In addition, CDCP1 expression on leukemic blasts and on cells with nonhematopoietic stem/progenitor cell phenotypes was determined. Here we demonstrate that a subset of bone marrow (BM), cord blood (CB), and mobilized peripheral blood (PB) CD34+ cells expressed this marker and that CDCP1 was detected on CD34+CD38 BM stem/progenitor cells but not on mature PB cells. Analysis of leukemic blasts from patients with acute lymphoblastic leukemia, acute myeloid leukemia, and chronic myeloid leukemia in blast crisis revealed that CDCP1 is predominantly expressed on CD34+CD133+ myeloid leukemic blasts. However, CDCP1 was not strictly correlated with CD34 and/or CD133 expression, suggesting that CDCP1 is a novel marker for leukemia diagnosis. Stimulation of CD34+ BM cells with CDCP1-reactive monoclonal antibody CUB1 resulted in an increased (~twofold) formation of erythroid colony-forming units, indicating that CDCP1 plays an important role in early hematopoiesis. Finally, we show that CDCP1 is also expressed on cells phenotypically identical to mesenchymal stem/progenitor cells (MSCs) and neural progenitor cells (NPCs). In conclusion, CDCP1 is not only a novel marker for immature hematopoietic progenitor cell subsets but also unique in its property to recognize cells with phenotypes reminiscent of MSC and NPC.




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