4.8 Article

A humanized bone marrow ossicle xenotransplantation model enables improved engraftment of healthy and leukemic human hematopoietic cells

Journal

NATURE MEDICINE
Volume 22, Issue 7, Pages 812-821

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nm.4103

Keywords

-

Funding

  1. Erwin-Schroedinger Research Fellowship (Austrian Science Fund)
  2. CJ Martin Overseas Biomedical Research Fellowship (NHMRC, Australia)
  3. New York Stem Cell Foundation
  4. National Institutes of Health [R01CA188055, U01HL099999]
  5. European Union [668724]
  6. Austrian Science Fund (FWF) [J 3358] Funding Source: researchfish

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available