Zeitschriftenaufsatz | 2019 Open Access

Identification of a leukemia-initiating stem cell in human mast cell leukemia

Autor:in
Eisenwort, Gregor; Sadovnik, Irina; Schwaab, Juliana; Jawhara, Mohamad; Keller, Alexandra; Stefanzl, G.; berger, daniela; Blatt, Katharina; Hoermann, Gregor; Bilban, Martin; Willman, Michael; Winding, Christiana; Sperr, Wolfgang R.; Arock, Michel; Ruelicke, Thomas; Reiter, Andreas; Valent, Peter
Publikationen als Autor:in / Herausgeber:in der Vetmeduni
Journal
Abstrakt
Mast cell leukemia (MCL) is a highly fatal malignancy characterized by devastating expansion of immature mast cells in various organs. Although considered a stem cell disease, little is known about MCL-propagating neoplastic stem cells. We here describe that leukemic stem cells (LSCs) in MCL reside within a CD34(+)/CD38(-) fraction of the clone. Whereas highly purified CD34(+)/CD38(-) cells engrafted NSG(hSCF) mice with fully manifesting MCL, no MCL was produced by CD34(+)/CD38(+) progenitors or the bulk of KIT+/CD34(-) mast cells. CD34(+)/CD38(-) MCL cells invariably expressed CD13 and CD133, and often also IL-1RAP, but did not express CD25, CD26 or CLL-1. CD34(+)/CD38(-) MCL cells also displayed several surface targets, including CD33, which was homogenously expressed on MCL LSCs in all cases, and the D816V mutant form of KIT. Although CD34(+)/CD38(-) cells were resistant against single drugs, exposure to combinations of CD33-targeting and KIT-targeting drugs resulted in LSC-depletion and markedly reduced engraftment in NSG(hSCF) mice. Together, MCL LSCs are CD34(+)/CD38(-) cells that express distinct profiles of markers and target antigens. Characterization of MCL LSCs should facilitate their purification and should support the development of LSC-eradicating curative treatment approaches in this fatal type of leukemia.
Schlagwörter
ADP-ribosyl Cyclase 1metabolism; Adult; Aged; Aged, 80 and over; Animals; Antigens, CD34metabolism; Cell Transformation, Neoplastic; Dipeptidyl Peptidase 4metabolism; Female; Gene Expression Regulation, Leukemic; Humans; Immunophenotyping; Interleukin-2 Receptor alpha Subunitmetabolism; Leukemiapathology; Leukemia, Mast-Cellpathology; Leukemia, Myeloid, Acutepathology; Male; Mice; Mice, Inbred NOD; Mice, SCID; Middle Aged; Neoplastic Stem Cellsclassificationcytology; Sialic Acid Binding Ig-like Lectin 3metabolism; Transplantation, Heterologous
Dokumententyp
Originalarbeit
CC Lizenz
CCBY
Open Access Type
Hybrid
ISSN/eISSN
0887-6924 - 1476-5551

Weitere Details

Band
33
Startseite
2673
letzte Seite
2684
Nummer
11
Seitenanzahl
12