Cargando…

Superselective intra-arterial umbilical cord blood administration to BM in experimental animals

Umbilical cord blood (UCB) as a source of hematopoietic stem cells for transplantation is limited by the low number of cells and delayed engraftment. UCB cells are infused i.v. for transplantation, although only a proportion of the cells reach the BM. We investigated whether UCB could be administere...

Descripción completa

Detalles Bibliográficos
Autores principales: Arnberg, F, Lundberg, J, Kenne, E, Jaff, N, Müller, P, Nava, S, Kaipe, H, Ringdén, O, Holmin, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261140/
https://www.ncbi.nlm.nih.gov/pubmed/25198791
http://dx.doi.org/10.1038/bmt.2014.190
_version_ 1782348262754222080
author Arnberg, F
Lundberg, J
Kenne, E
Jaff, N
Müller, P
Nava, S
Kaipe, H
Ringdén, O
Holmin, S
author_facet Arnberg, F
Lundberg, J
Kenne, E
Jaff, N
Müller, P
Nava, S
Kaipe, H
Ringdén, O
Holmin, S
author_sort Arnberg, F
collection PubMed
description Umbilical cord blood (UCB) as a source of hematopoietic stem cells for transplantation is limited by the low number of cells and delayed engraftment. UCB cells are infused i.v. for transplantation, although only a proportion of the cells reach the BM. We investigated whether UCB could be administered safely using superselective intra-arterial (i.a.) injection. We injected human UCB (5 × 10(6)) into the aorta in rats, into the iliac artery in mice and into the femoral nutrient artery (FNA) in rabbits. We used angiography, immunohistochemistry, intravital microscopy and qPCR to assess safety end points and the distribution of injected cells. All animals showed normal behavior. No evidence of organ infarction was noted. UCB injected into the FNA of rabbits did not change the flow rates, measured by angiography. By qPCR, we found significantly higher fold-change values in the injected BM compared with i.v. injection (P=0.0087). Using intravital microscopy we visualized the mouse capillary bed during i.a. injection without cellular congestion. In summary, we show that i.a. infusion of UCB is safe and reaches an eightfold increase in engraftment in the BM compared with i.v. infusion. These studies lay the foundation for clinical trials.
format Online
Article
Text
id pubmed-4261140
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-42611402014-12-15 Superselective intra-arterial umbilical cord blood administration to BM in experimental animals Arnberg, F Lundberg, J Kenne, E Jaff, N Müller, P Nava, S Kaipe, H Ringdén, O Holmin, S Bone Marrow Transplant Original Article Umbilical cord blood (UCB) as a source of hematopoietic stem cells for transplantation is limited by the low number of cells and delayed engraftment. UCB cells are infused i.v. for transplantation, although only a proportion of the cells reach the BM. We investigated whether UCB could be administered safely using superselective intra-arterial (i.a.) injection. We injected human UCB (5 × 10(6)) into the aorta in rats, into the iliac artery in mice and into the femoral nutrient artery (FNA) in rabbits. We used angiography, immunohistochemistry, intravital microscopy and qPCR to assess safety end points and the distribution of injected cells. All animals showed normal behavior. No evidence of organ infarction was noted. UCB injected into the FNA of rabbits did not change the flow rates, measured by angiography. By qPCR, we found significantly higher fold-change values in the injected BM compared with i.v. injection (P=0.0087). Using intravital microscopy we visualized the mouse capillary bed during i.a. injection without cellular congestion. In summary, we show that i.a. infusion of UCB is safe and reaches an eightfold increase in engraftment in the BM compared with i.v. infusion. These studies lay the foundation for clinical trials. Nature Publishing Group 2014-12 2014-09-08 /pmc/articles/PMC4261140/ /pubmed/25198791 http://dx.doi.org/10.1038/bmt.2014.190 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Original Article
Arnberg, F
Lundberg, J
Kenne, E
Jaff, N
Müller, P
Nava, S
Kaipe, H
Ringdén, O
Holmin, S
Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title_full Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title_fullStr Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title_full_unstemmed Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title_short Superselective intra-arterial umbilical cord blood administration to BM in experimental animals
title_sort superselective intra-arterial umbilical cord blood administration to bm in experimental animals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261140/
https://www.ncbi.nlm.nih.gov/pubmed/25198791
http://dx.doi.org/10.1038/bmt.2014.190
work_keys_str_mv AT arnbergf superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT lundbergj superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT kennee superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT jaffn superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT mullerp superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT navas superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT kaipeh superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT ringdeno superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals
AT holmins superselectiveintraarterialumbilicalcordbloodadministrationtobminexperimentalanimals