| Literature DB >> 27683414 |
Jin Li1, Tamara Riedt1, Steven Goossens2,3,4, Carmen Carrillo García1, Sabrina Szczepanski1, Maria Brandes1, Tim Pieters2,3,4, Linne Dobrosch1, Ines Gütgemann5, Natalie Farla2,3, Enrico Radaelli6,7, Paco Hulpiau2,3, Nikhil Mallela8, Holger Fröhlich8, Roberta La Starza9, Caterina Matteucci9, Tong Chen10, Peter Brossart1, Cristina Mecucci9, Danny Huylebroeck11,12, Jody J Haigh13, Viktor Janzen1.
Abstract
Epithelial-to-mesenchymal-transition (EMT) is critical for normal embryogenesis and effective postnatal wound healing, but is also associated with cancer metastasis. SNAIL, ZEB, and TWIST families of transcription factors are key modulators of the EMT process, but their precise roles in adult hematopoietic development and homeostasis remain unclear. Here we report that genetic inactivation of Zeb2 results in increased frequency of stem and progenitor subpopulations within the bone marrow (BM) and spleen and that these changes accompany differentiation defects in multiple hematopoietic cell lineages. We found no evidence that Zeb2 is critical for hematopoietic stem cell self-renewal capacity. However, knocking out Zeb2 in the BM promoted a phenotype with several features that resemble human myeloproliferative disorders, such as BM fibrosis, splenomegaly, and extramedullary hematopoiesis. Global gene expression and intracellular signal transduction analysis revealed perturbations in specific cytokine and cytokine receptor-related signaling pathways following Zeb2 loss, especially the JAK-STAT and extracellular signal-regulated kinase pathways. Moreover, we detected some previously unknown mutations within the human Zeb2 gene (ZFX1B locus) from patients with myeloid disease. Collectively, our results demonstrate that Zeb2 controls adult hematopoietic differentiation and lineage fidelity through widespread modulation of dominant signaling pathways that may contribute to blood disorders.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27683414 DOI: 10.1182/blood-2016-05-714659
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113