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Trisomy 21 Enhances Human Fetal Erythro-megakaryocytic Development

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2008 Sep 25
PMID 18812473
Citations 64
Authors
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Abstract

Children with Down syndrome exhibit 2 related hematopoietic diseases: transient myeloproliferative disorder (TMD) and acute megakaryoblastic leukemia (AMKL). Both exhibit clonal expansion of blasts with biphenotypic erythroid and megakaryocytic features and contain somatic GATA1 mutations. While altered GATA1 inhibits erythro-megakaryocytic development, less is known about how trisomy 21 impacts blood formation, particularly in the human fetus where TMD and AMKL originate. We used in vitro and mouse transplantation assays to study hematopoiesis in trisomy 21 fetal livers with normal GATA1 alleles. Remarkably, trisomy 21 progenitors exhibited enhanced production of erythroid and megakaryocytic cells that proliferated excessively. Our findings indicate that trisomy 21 itself is associated with cell-autonomous expansion of erythro-megakaryocytic progenitors. This may predispose to TMD and AMKL by increasing the pool of cells susceptible to malignant transformation through acquired mutations in GATA1 and other cooperating genes.

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References
1.
Gurbuxani S, Vyas P, Crispino J . Recent insights into the mechanisms of myeloid leukemogenesis in Down syndrome. Blood. 2003; 103(2):399-406. DOI: 10.1182/blood-2003-05-1556. View

2.
Rainis L, Bercovich D, Strehl S, Teigler-Schlegel A, Stark B, Trka J . Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003; 102(3):981-6. DOI: 10.1182/blood-2002-11-3599. View

3.
Taub J, Mundschau G, Ge Y, Poulik J, Qureshi F, Jensen T . Prenatal origin of GATA1 mutations may be an initiating step in the development of megakaryocytic leukemia in Down syndrome. Blood. 2004; 104(5):1588-9. DOI: 10.1182/blood-2004-04-1563. View

4.
Ito E, Kasai M, Hayashi Y, Toki T, Arai K, Yokoyama S . Expression of erythroid-specific genes in acute megakaryoblastic leukaemia and transient myeloproliferative disorder in Down's syndrome. Br J Haematol. 1995; 90(3):607-14. DOI: 10.1111/j.1365-2141.1995.tb05591.x. View

5.
Hitzler J, Zipursky A . Origins of leukaemia in children with Down syndrome. Nat Rev Cancer. 2005; 5(1):11-20. DOI: 10.1038/nrc1525. View