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Disruption Of PML Nuclear Bodies Cooperates In The Pathogenesis Of Acute Promyelocytic Leukemia

Moravcsik, E, Joannides, M, Voisset, E, Stratford, EW, Zeisig, BB, Morris, J, Densham, R, Palgrave, CJ, Stamp, G, Nye, E, Hills, RK, Salomoni, P, So, CWE, Kogan, SC, Solomon, E and Grimwade, D (2013) Disruption Of PML Nuclear Bodies Cooperates In The Pathogenesis Of Acute Promyelocytic Leukemia In: 55th American Society of Hematology Annual Meeting, 2013-12-07 - 2013-12-10, Ernest N. Morial Convention Center, New Orleans.

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Abstract

Acute promyelocytic leukemia (APL) is characterised by the t(15;17)(q22;q21) leading to fusion of PML to the gene encoding the myeloid transcription factor Retinoic Acid Receptor α (RARα). Chromosomal translocations such as the t(15;17) are considered to be initiating events in leukemogenesis; however, sequencing of APL genomes has provided further evidence that the PML-RARα fusion is insufficient to induce leukemia, which depends upon the acquisition of cooperating mutations. The PML-RARα oncoprotein exerts a profound effect on nuclear architecture, disrupting multiprotein structures known as PML nuclear bodies (NBs). The function of these structures remains an enigma; however, their disruption in PML-RARα+ APL and acute lymphoblastic leukemia with the t(9;15)(p13;q24)/PAX5-PML fusion is associated with delocalisation of a number of component proteins including PML, which have been implicated in growth control and neoplastic transformation. It is now established that the PML moiety contributes to APL pathogenesis by conferring via the translocation a novel dimerisation capacity to RARα, but it has been unclear whether deregulation of PML and other NB components cooperates in leukemic transformation or impacts the response to differentiating agents. To address these questions, we generated a knock-in mouse model with targeted NB disruption achieved through mutation of key zinc-binding cysteine residues in the amino-terminal RING domain of Pml. Homozygous Pml RING mutant mice are viable, with no overt developmental defect; however, analysis of the bone marrow revealed significant expansion of the Lin(-)Sca-1(+)c-Kit(+) (LSK) population compared to wild type (WT) controls (p<0.01), accompanied by increased LSK cell proliferation (p<0.0001) as evaluated by in vivo labelling through incorporation of 5-ethynyl-2'-deoxyuridine (EdU). In addition, hematopoietic cells derived from homozygous Pml RING mutant mice exhibited markedly elevated levels of DNA damage compared to WT cells from age-matched controls, as evidenced by increased numbers of γH2AX foci (p=0.009). This was associated with significantly delayed DNA damage repair responses in Pml RING mutant cells following γ-irradiation (p=0.005). Accordingly, expression of PML-RARα in human hematopoietic cells, which led to disruption of NBs, also induced a significant increase in γH2AX foci (p=0.0023). While no leukemias arose in homozygous Pml RING mutant mice, they developed an excess of T- and B-cell lymphomas (p=0.03), consistent with the proposed tumour suppressor function of PML and the NBs. Since a key property conferred by the PML moiety required for leukemogenicity of the PML-RARα oncoprotein is the capacity to dimerise, we evaluated whether Pml NB disruption could cooperate with forced RARα homodimerisation (mediated artificially by linking RARα to the p50 dimerisation motif of NFκB). While Pml NB disruption or p50-RARA expressed under the control of the MRP8 promoter in murine hematopoietic stem/progenitor cells conferred limited replating capacity, in combination they exhibited marked cooperativity, with a significant increase in third round colonies (p=0.03). Moreover, NB disruption was found to cooperate with forced RARα homodimerisation in vivo with a doubling in the rate of leukemia development in p50-RARα mice with mutated Pml (p<0.0001), leading to a penetrance comparable to that observed in previously published PML-RARα transgenic models. Moreover, the latency to onset of leukemia was significantly shorter in p50-RARα mice with the Pml RING mutation, occurring from 213 days of age vs 310 days with WT Pml (p=0.008). While Pml NB disruption did not affect engraftment of p50-RARα leukemias in serial transplantation, the in vitro differentiation response of p50-RARα leukemias to All transretinoic acid (ATRA) as determined by nitroblue tetrazolium assay was significantly impaired in the context of NB disruption (p<0.05). Moreover, prolongation of survival following ATRA treatment in mice transplanted with p50-RARα leukemic blasts was dependent upon Pml NB integrity (p=0.03). Overall, these data suggest that the NB disruption mediated by the PML-RARα oncoprotein plays a key role in APL pathogenesis contributing to expansion of the LSK population and defective DNA repair predisposing to the acquisition of cooperating mutations, but also implicate NBs in the response to differentiating agents.

Item Type: Conference or Workshop Item (Conference Abstract)
Subjects : Veterinary Medicine
Divisions : Faculty of Health and Medical Sciences > School of Veterinary Medicine
Authors :
AuthorsEmailORCID
Moravcsik, EUNSPECIFIEDUNSPECIFIED
Joannides, MUNSPECIFIEDUNSPECIFIED
Voisset, EUNSPECIFIEDUNSPECIFIED
Stratford, EWUNSPECIFIEDUNSPECIFIED
Zeisig, BBUNSPECIFIEDUNSPECIFIED
Morris, JUNSPECIFIEDUNSPECIFIED
Densham, RUNSPECIFIEDUNSPECIFIED
Palgrave, CJUNSPECIFIEDUNSPECIFIED
Stamp, GUNSPECIFIEDUNSPECIFIED
Nye, EUNSPECIFIEDUNSPECIFIED
Hills, RKUNSPECIFIEDUNSPECIFIED
Salomoni, PUNSPECIFIEDUNSPECIFIED
So, CWEUNSPECIFIEDUNSPECIFIED
Kogan, SCUNSPECIFIEDUNSPECIFIED
Solomon, EUNSPECIFIEDUNSPECIFIED
Grimwade, DUNSPECIFIEDUNSPECIFIED
Date : 15 November 2013
Copyright Disclaimer : Copyright 2013 The American Society of Hematology
Contributors :
ContributionNameEmailORCID
UNSPECIFIEDThe American Society of Hematology, UNSPECIFIEDUNSPECIFIED
Additional Information : Full text not available from this repository
Depositing User : Symplectic Elements
Date Deposited : 06 Sep 2016 17:28
Last Modified : 06 Sep 2016 17:28
URI: http://epubs.surrey.ac.uk/id/eprint/811929

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