| Literature DB >> 28679949 |
V Lokesh Battula1,2, Phuong M Le1, Jeffrey C Sun1, Khoa Nguyen1, Bin Yuan1, Ximin Zhou1, Sonali Sonnylal1, Teresa McQueen1, Vivian Ruvolo1, Keith A Michel3, Xiaoyang Ling1, Rodrigo Jacamo1, Elizabeth Shpall4, Zhiqiang Wang5, Arvind Rao6, Gheath Al-Atrash4, Marina Konopleva1, R Eric Davis5, Melvyn A Harrington7, Catherine W Cahill7, Carlos Bueso-Ramos8, Michael Andreeff1,4.
Abstract
Genotypic and phenotypic alterations in the bone marrow (BM) microenvironment, in particular in osteoprogenitor cells, have been shown to support leukemogenesis. However, it is unclear how leukemia cells alter the BM microenvironment to create a hospitable niche. Here, we report that acute myeloid leukemia (AML) cells, but not normal CD34+ or CD33+ cells, induce osteogenic differentiation in mesenchymal stromal cells (MSCs). In addition, AML cells inhibited adipogenic differentiation of MSCs. Mechanistic studies identified that AML-derived BMPs activate Smad1/5 signaling to induce osteogenic differentiation in MSCs. Gene expression array analysis revealed that AML cells induce connective tissue growth factor (CTGF) expression in BM-MSCs irrespective of AML type. Overexpression of CTGF in a transgenic mouse model greatly enhanced leukemia engraftment in vivo. Together, our data suggest that AML cells induce a preosteoblast-rich niche in the BM that in turn enhances AML expansion.Entities:
Keywords: Bone Biology; Stem cells
Year: 2017 PMID: 28679949 PMCID: PMC5499365 DOI: 10.1172/jci.insight.90036
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708