A humanized bone marrow ossicle xenotransplantation model enables improved engraftment of healthy and leukemic human hematopoietic cells.
Andreas ReinischDaniel ThomasM Ryan CorcesXiaohua ZhangDita A GratzingerWan-Jen HongKatharina SchallmoserDirk StrunkRavindra MajetiPublished in: Nature medicine (2016)
Xenotransplantation models represent powerful tools for the investigation of healthy and malignant human hematopoiesis. However, current models do not fully mimic the components of the human bone marrow (BM) microenvironment, and they enable only limited engraftment of samples from some human malignancies. Here we show that a xenotransplantation model bearing subcutaneous humanized ossicles with an accessible BM microenvironment, formed by in situ differentiation of human BM-derived mesenchymal stromal cells, enables the robust engraftment of healthy human hematopoietic stem and progenitor cells, as well as primary acute myeloid leukemia (AML) samples, at levels much greater than those in unmanipulated mice. Direct intraossicle transplantation accelerated engraftment and resulted in the detection of substantially higher leukemia-initiating cell (LIC) frequencies. We also observed robust engraftment of acute promyelocytic leukemia (APL) and myelofibrosis (MF) samples, and identified LICs in these malignancies. This humanized ossicle xenotransplantation approach provides a system for modeling a wide variety of human hematological diseases.
Keyphrases
- endothelial cells
- bone marrow
- acute myeloid leukemia
- induced pluripotent stem cells
- pluripotent stem cells
- mesenchymal stem cells
- cell therapy
- insulin resistance
- adipose tissue
- signaling pathway
- acute lymphoblastic leukemia
- metabolic syndrome
- quantum dots
- single cell
- liver failure
- cell death
- acute respiratory distress syndrome
- wild type
- cell cycle arrest
- loop mediated isothermal amplification