Erythroid lineage-restricted expression of Jak2V617F is sufficient to induce a myeloproliferative disease in mice

被引:4
作者
Akada, Hajime [1 ]
Akada, Saeko [1 ]
Hutchison, Robert E. [2 ]
Mohi, Golam [1 ]
机构
[1] SUNY Upstate Med Univ, Dept Pharmacol, Syracuse, NY 13210 USA
[2] SUNY Upstate Med Univ, Dept Pathol, Syracuse, NY 13210 USA
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 09期
关键词
Jak2V617F; MPNs; erythroid progenitors; ACUTE MYELOID-LEUKEMIA; TYROSINE KINASE JAK2; VERA-LIKE DISEASE; POLYCYTHEMIA-VERA; HEMATOPOIETIC STEM; ESSENTIAL THROMBOCYTHEMIA; MOUSE MODEL; MUTATION; CELL; DISORDERS;
D O I
10.3324/haematol.2011.059113
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The JAK2V617F mutation has been found in most cases of Phnegative myeloproliferative neoplasms. Recent studies have shown that expression of Jak2V617F in the hematopoietic compartment causes marked expansion of erythroid progenitors and their transformation to cytokine-independence. To determine if erythroid progenitors are the target cells for induction and propagation of Jak2V617F-evoked myeloproliferative neoplasm, we used a conditional Jak2V617F knock-in mouse and an erythroid-lineage specific EpoRCre line. Erythroid-specific expression of heterozygous or homozygous Jak2V617F resulted in a polycythemia-like phenotype characterized by increase in hematocrit and hemoglobin, increased red blood cells, erythropoietin-independent erythroid colonies and splenomegaly. Transplantation of Jak2V617F-expressing erythroid progenitors from the diseased mice into secondary recipients could not propagate the disease. Our results suggest that erythroid lineage-restricted expression of Jak2V617F is sufficient to induce a polycythemia-like disease in a gene-dose dependent manner. Jak2V617F mutation, however, does not confer leukemia stem cell-like properties to erythroid progenitors.
引用
收藏
页码:1389 / 1393
页数:5
相关论文
共 24 条
[1]   Conditional expression of heterozygous or homozygous Jak2V617F from its endogenous promoter induces a polycythemia vera-like disease [J].
Akada, Hajime ;
Yan, Dongqing ;
Zou, Haiying ;
Fiering, Steven ;
Hutchison, Robert E. ;
Mohi, M. Golam .
BLOOD, 2010, 115 (17) :3589-3597
[2]   Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders [J].
Baxter, EJ ;
Scott, LM ;
Campbell, PJ ;
East, C ;
Fourouclas, N ;
Swanton, S ;
Vassiliou, GS ;
Bench, AJ ;
Boyd, EM ;
Curtin, N ;
Scott, MA ;
Erber, WN ;
Green, AR .
LANCET, 2005, 365 (9464) :1054-1061
[3]   Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737
[4]   The JAK2 617V>F mutation triggers erythropoietin hypersensitivity and terminal erythroid amplification in primary cells from patients with polycythemia vera [J].
Dupont, Sabrina ;
Masse, Aline ;
James, Chloe ;
Teyssandier, Irene ;
Lecluse, Yann ;
Larbret, Frederic ;
Ugo, Valerie ;
Saulnier, Patrick ;
Koscielny, Serge ;
Le Couedic, Jean Pierre ;
Casadevall, Nicole ;
Vainchenker, William ;
Delhommeau, Francois .
BLOOD, 2007, 110 (03) :1013-1021
[5]   Selective inhibition of JAK2-Driven erythroid differentiation of polycythemia vera progenitors [J].
Geron, Ifat ;
Abrahamsson, Annelie E. ;
Barroga, Charlene F. ;
Kavalerchik, Edward ;
Gotlib, Jason ;
Hood, John D. ;
Durocher, Jeffrey ;
Mak, Chi Ching ;
Noronha, Glenn ;
Soll, Richard M. ;
Tefferi, Ayalew ;
Kaushansky, Ken ;
Jamieson, Catriona H. M. .
CANCER CELL, 2008, 13 (04) :321-330
[6]   Identification of a myeloid committed progenitor as the cancer-initiating cell in acute promyelocytic leukemia [J].
Guibal, Florence C. ;
Alberich-Jorda, Meritxell ;
Hirai, Hideyo ;
Ebralidze, Alexander ;
Levantini, Elena ;
Di Ruscio, Annalisa ;
Zhang, Pu ;
Santana-Lemos, Barbara A. ;
Neuberg, Donna ;
Wagers, Amy J. ;
Rego, Eduardo M. ;
Tenen, Daniel G. .
BLOOD, 2009, 114 (27) :5415-5425
[7]   A mouse model for visualization and conditional mutations in the erythroid lineage [J].
Heinrich, AC ;
Pelanda, R ;
Klingmüller, U .
BLOOD, 2004, 104 (03) :659-666
[8]   MOZ-TIF2, but not BCR-ABL, confers properties of leukemic stem cells to committed murine hematopoietic progenitors [J].
Huntly, BJP ;
Shigematsu, H ;
Deguchi, K ;
Lee, BH ;
Mizuno, S ;
Duclos, N ;
Rowan, R ;
Amaral, S ;
Curley, D ;
Williams, IR ;
Akashi, K ;
Gilliland, DG .
CANCER CELL, 2004, 6 (06) :587-596
[9]   A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera [J].
James, C ;
Ugo, V ;
Le Couédic, JP ;
Staerk, J ;
Delhommeau, F ;
Lacout, C ;
Garçon, L ;
Raslova, H ;
Berger, R ;
Bennaceur-Griscelli, A ;
Villeval, JL ;
Constantinescu, SN ;
Casadevall, N ;
Vainchenker, W .
NATURE, 2005, 434 (7037) :1144-1148
[10]   The JAK2 V617F mutation occurs in hematopoietic stem cells in polycythemia vera and predisposes toward erythroid differentiation [J].
Jamieson, CHM ;
Gotlib, J ;
Durocher, JA ;
Chao, MP ;
Mariappan, MR ;
Lay, M ;
Jones, C ;
Zehnder, JL ;
Lilleberg, SL ;
Weissman, IL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (16) :6224-6229