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The cell fate determinant Llgl1 influences HSC fitness and prognosis in AML

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Item Type:Article
Title:The cell fate determinant Llgl1 influences HSC fitness and prognosis in AML
Creators Name:Heidel, Florian H., Bullinger, Lars, Arreba-Tutusaus, Patricia, Wang, Zhu, Gaebel, Julia, Hirt, Carsten, Niederwieser, Dietger, Lane, Steven W., Döhner, Konstanze, Vasioukhin, Valera, Fischer, Thomas and Armstrong, Scott A.
Abstract:A unique characteristic of hematopoietic stem cells (HSCs) is the ability to self-renew. Several genes and signaling pathways control the fine balance between self-renewal and differentiation in HSCs and potentially also in leukemia stem cells. Recently, studies have shed light on developmental molecules and evolutionarily conserved signals as regulators of stem cells in hematopoiesis and leukemia. In this study, we provide evidence that the cell fate determinant Llgl1 (lethal giant larvae homolog 1) plays an important role in regulation of HSCs. Loss of Llgl1 leads to an increase in HSC numbers that show increased repopulation capacity and competitive advantage after transplantation. This advantage increases upon serial transplantation or when stress is applied to HSCs. Llgl1−/− HSCs show increased cycling but neither exhaust nor induce leukemia in recipient mice. Llgl1 inactivation is associated with transcriptional repression of transcription factors such as KLF4 (Krüppel-like factor 4) and EGR1 (early-growth-response 1) that are known inhibitors of HSC self-renewal. Decreased Llgl1 expression in human acute myeloid leukemia (AML) cells is associated with inferior patient survival. Thus, inactivation of Llgl1 enhances HSC self-renewal and fitness and is associated with unfavorable outcome in human AML.
Keywords:Acute Myeloid Leukemia, Cytoskeletal Proteins, Early Growth Response Protein 1, Hematopoietic Stem Cell Transplantation, Hematopoietic Stem Cells, Inbred C57BL Mice, Kruppel-Like Factor 4, Kruppel-Like Transcription Factors, Leukemic Gene Expression Regulation, Mutant Strains Mice, Prognosis, Animals, Mice
Source:Journal of Experimental Medicine
ISSN:0022-1007
Publisher:Rockefeller University Press
Volume:210
Number:1
Page Range:15-22
Date:14 January 2013
Official Publication:https://doi.org/10.1084/jem.20120596
PubMed:View item in PubMed

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