Abstract

Intra-bone marrow transplantation (IBMT) has been adapted for mouse models to improve the seeding efficiency of transplanted hematopoietic stem and progenitor cells. Commonly used injection volumes for IBMT into the tibia differ between 10 and 40 μL even though considerable amounts of injected cells leak into the blood circulation immediately after injection. Injection of 3 μL trypan blue into the tibia of dead BALB/c mice showed staining in large vessels of hind limbs, even without supporting circulation. We therefore tested the effective capacity of the medullary cavity of dissected tibiae and femora of different mouse strains by bioluminescence imaging after injection of luciferase expressing cells. Cell leakage was already observed at 3 μL of injection volume and the measured emission rate increased significantly when 5 and 10 μL of volume with the same cell concentration were injected. Surprisingly, increasing injection volumes containing constant cell amounts resulted in comparable emission rates, suggesting a similar amount of leaked and absorbed cells independent of the injection volume. However, the absorption of a specific amount of injected cells could not be confirmed, as the ratio of leaked to absorbed cells was similar between IBMT that were performed with a constant injection volume containing either low or high cell amounts. In summary, for optimal cell transplantation via IBMT in mice we suggest to inject a high concentrated cell suspension with a maximum injection volume of 3 μL.

Highlights

  • Xenotransplantation assay in mice is an important approach to investigate biology of the human hematopoietic stem and progenitor cells (HS/PCs)

  • Leukemic stem cells (LSCs) including their repopulation and differentiation capacity after transplantation into mouse models are of particular interest in the investigation of different forms of myeloid and lymphatic leukemia [1]

  • The great majority of transplanted cells are retained in the lung and other organs like the liver, kidneys and spleen [2,3,4]. This stem cell trafficking vastly reduces the number of cells entering the bone marrow (BM) and might trigger a qualitative selection of donor cell subpopulations

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Summary

Introduction

Xenotransplantation assay in mice is an important approach to investigate biology of the human hematopoietic stem and progenitor cells (HS/PCs). Donor cell transplantation in mice is mostly performed by intravenous (i.v.) injection into the lateral tail vein and injected cells must pass through the lung before they enter the systemic. The great majority of transplanted cells are retained in the lung and other organs like the liver, kidneys and spleen [2,3,4]. This stem cell trafficking vastly reduces the number of cells entering the bone marrow (BM) and might trigger a qualitative selection of donor cell subpopulations

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