Rapid development of myeloproliferative neoplasm in mice with PTPN11D61Y mutation and haploinsufficient for Dnmt3a

Lisa Deng, Briana M. Richine, Elizabeth L. Virts, Victoria N. Jideonwo-Auman, Rebecca Chan, Reuben Kapur

Research output: Contribution to journalArticle

Abstract

PTPN11 gain-of-function mutation is the most common mutation found in patients with juvenile myelomonocytic leukemia and DNMT3A loss occurs in over 20% of acute myeloid leukemia patients. We studied the combined effect of both Ptpn11 gain-offunction mutation (D61Y) and Dnmt3a haploinsufficiency on mouse hematopoiesis, the presence of which has been described in both juvenile myelomonocytic leukemia and acute myeloid leukemia patients. Double mutant mice rapidly become moribund relative to any of the other genotypes, which is associated with enlargement of the spleen and an increase in white blood cell counts. An increase in the mature myeloid cell compartment as reflected by the presence of Gr1+Mac1+ cells was also observed in double mutant mice relative to any other group. Consistent with these observations, a significant increase in the absolute number of granulocyte macrophage progenitors (GMPs) was seen in double mutant mice. A decrease in the lymphoid compartment including both T and B cells was noted in the double mutant mice. Another significant difference was the presence of extramedullary erythropoiesis with increased erythroid progenitors in the spleens of Dnmt3a+/-;D61Y mice relative to other groups. Taken together, our results suggest that the combined haploinsufficiency of Dnmt3a and presence of an activated Shp2 changes the composition of multiple hematopoietic lineages in mice relative to the individual heterozygosity of these genes.

Original languageEnglish (US)
Pages (from-to)6055-6061
Number of pages7
JournalOncotarget
Volume9
Issue number5
DOIs
StatePublished - Jan 1 2018

Fingerprint

Mutation
Juvenile Myelomonocytic Leukemia
Neoplasms
Haploinsufficiency
Acute Myeloid Leukemia
Spleen
Granulocyte-Macrophage Progenitor Cells
Erythropoiesis
Hematopoiesis
Myeloid Cells
Leukocyte Count
B-Lymphocytes
Genotype
T-Lymphocytes
Genes

Keywords

  • AML
  • DNMT3A
  • JMML
  • Myeloproliferation
  • SHP2

ASJC Scopus subject areas

  • Oncology

Cite this

Rapid development of myeloproliferative neoplasm in mice with PTPN11D61Y mutation and haploinsufficient for Dnmt3a. / Deng, Lisa; Richine, Briana M.; Virts, Elizabeth L.; Jideonwo-Auman, Victoria N.; Chan, Rebecca; Kapur, Reuben.

In: Oncotarget, Vol. 9, No. 5, 01.01.2018, p. 6055-6061.

Research output: Contribution to journalArticle

Deng, Lisa ; Richine, Briana M. ; Virts, Elizabeth L. ; Jideonwo-Auman, Victoria N. ; Chan, Rebecca ; Kapur, Reuben. / Rapid development of myeloproliferative neoplasm in mice with PTPN11D61Y mutation and haploinsufficient for Dnmt3a. In: Oncotarget. 2018 ; Vol. 9, No. 5. pp. 6055-6061.
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