Diverse marrow stromal cells protect CLL cells from spontaneous and drug-induced apoptosis: development of a reliable and reproducible system to assess stromal cell adhesion-mediated drug resistance

Antonina V. Kurtova(Leukemia Research Foundation), Kumudha Balakrishnan(The University of Texas MD Anderson Cancer Center), Rong Chen(The University of Texas MD Anderson Cancer Center), Wei Ding(Mayo Clinic in Arizona), Susanne Schnabl(Medical University of Vienna), Maite P. Quiroga(Leukemia Research Foundation), Mariela Sivina(Leukemia Research Foundation), William G. Wierda(Leukemia Research Foundation), Zeev Estrov(Leukemia Research Foundation), Michael J. Keating(Leukemia Research Foundation), Medhat Shehata(Medical University of Vienna), Ulrich Jäger(Medical University of Vienna), Varsha Gandhi(The University of Texas MD Anderson Cancer Center), Neil E. Kay(Mayo Clinic in Arizona), William Plunkett(The University of Texas MD Anderson Cancer Center), Jan A. Burger(Leukemia Research Foundation)
Blood
September 18, 2009
Cited by 317Open Access
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Abstract

Marrow stromal cells (MSCs) provide important survival and drug resistance signals to chronic lymphocytic leukemia (CLL) cells, but current models to analyze CLL-MSC interactions are heterogeneous. Therefore, we tested different human and murine MSC lines and primary human MSCs for their ability to protect CLL cells from spontaneous and drug-induced apoptosis. Our results show that both human and murine MSCs are equally effective in protecting CLL cells from fludarabine-induced apoptosis. This protective effect was sustained over a wide range of CLL-MSC ratios (5:1 to 100:1), and the levels of protection were reproducible in 4 different laboratories. Human and murine MSCs also protected CLL cells from dexamethasone- and cyclophosphamide-induced apoptosis. This protection required cell-cell contact and was virtually absent when CLL cells were separated from the MSCs by micropore filters. Furthermore, MSCs maintained Mcl-1 and protected CLL cells from spontaneous and fludarabine-induced Mcl-1 and PARP cleavage. Collectively, these studies define common denominators for CLL cocultures with MSCs. They also provide a reliable, validated tool for future investigations into the mechanism of MSC-CLL cross talk and for drug testing in a more relevant fashion than the commonly used suspension cultures.


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