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Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose

PURPOSE: Ablative bone marrow irradiation is an integral part of hematopoietic stem cell transplantation. These treatment regimens are based on classically held models of radiation dose and the bone marrow response. Flt-3 ligand (FL) has been suggested as a marker of hematopoiesis and bone marrow st...

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Autores principales: Sproull, Mary, Avondoglio, Dane, Kramp, Tamalee, Shankavaram, Uma, Camphausen, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591371/
https://www.ncbi.nlm.nih.gov/pubmed/23505536
http://dx.doi.org/10.1371/journal.pone.0058558
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author Sproull, Mary
Avondoglio, Dane
Kramp, Tamalee
Shankavaram, Uma
Camphausen, Kevin
author_facet Sproull, Mary
Avondoglio, Dane
Kramp, Tamalee
Shankavaram, Uma
Camphausen, Kevin
author_sort Sproull, Mary
collection PubMed
description PURPOSE: Ablative bone marrow irradiation is an integral part of hematopoietic stem cell transplantation. These treatment regimens are based on classically held models of radiation dose and the bone marrow response. Flt-3 ligand (FL) has been suggested as a marker of hematopoiesis and bone marrow status but the kinetics of its response to bone marrow irradiation has yet to be fully characterized. In the current study, we examine plasma FL response to total body and partial body irradiation in mice and its relationship with irradiation dose, time of collection and pattern of bone marrow exposure. MATERIALS/METHODS: C57BL6 mice received a single whole body or partial body irradiation dose of 1–8 Gy. Plasma was collected by mandibular or cardiac puncture at 24, 48 and 72 hr post-irradiation as well as 1–3 weeks post-irradiation. FL levels were determined via ELISA assay and used to generate two models: a linear regression model and a gated values model correlating plasma FL levels with radiation dose. RESULTS: At all doses between 1–8 Gy, plasma FL levels were greater than control and the level of FL increased proportionally to the total body irradiation dose. Differences in FL levels were statistically significant at each dose and at all time points. Partial body irradiation of the trunk areas, encompassing the bulk of the hematopoietically active bone marrow, resulted in significantly increased FL levels over control but irradiation of only the head or extremities did not. FL levels were used to generate a dose prediction model for total body irradiation. In a blinded study, the model differentiated mice into dose received cohorts of 1, 4 or 8 Gy based on plasma FL levels at 24 or 72 hrs post-irradiation. CONCLUSION: Our findings indicate that plasma FL levels might be used as a marker of hematopoietically active bone marrow and radiation exposure in mice.
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spelling pubmed-35913712013-03-15 Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose Sproull, Mary Avondoglio, Dane Kramp, Tamalee Shankavaram, Uma Camphausen, Kevin PLoS One Research Article PURPOSE: Ablative bone marrow irradiation is an integral part of hematopoietic stem cell transplantation. These treatment regimens are based on classically held models of radiation dose and the bone marrow response. Flt-3 ligand (FL) has been suggested as a marker of hematopoiesis and bone marrow status but the kinetics of its response to bone marrow irradiation has yet to be fully characterized. In the current study, we examine plasma FL response to total body and partial body irradiation in mice and its relationship with irradiation dose, time of collection and pattern of bone marrow exposure. MATERIALS/METHODS: C57BL6 mice received a single whole body or partial body irradiation dose of 1–8 Gy. Plasma was collected by mandibular or cardiac puncture at 24, 48 and 72 hr post-irradiation as well as 1–3 weeks post-irradiation. FL levels were determined via ELISA assay and used to generate two models: a linear regression model and a gated values model correlating plasma FL levels with radiation dose. RESULTS: At all doses between 1–8 Gy, plasma FL levels were greater than control and the level of FL increased proportionally to the total body irradiation dose. Differences in FL levels were statistically significant at each dose and at all time points. Partial body irradiation of the trunk areas, encompassing the bulk of the hematopoietically active bone marrow, resulted in significantly increased FL levels over control but irradiation of only the head or extremities did not. FL levels were used to generate a dose prediction model for total body irradiation. In a blinded study, the model differentiated mice into dose received cohorts of 1, 4 or 8 Gy based on plasma FL levels at 24 or 72 hrs post-irradiation. CONCLUSION: Our findings indicate that plasma FL levels might be used as a marker of hematopoietically active bone marrow and radiation exposure in mice. Public Library of Science 2013-03-07 /pmc/articles/PMC3591371/ /pubmed/23505536 http://dx.doi.org/10.1371/journal.pone.0058558 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Sproull, Mary
Avondoglio, Dane
Kramp, Tamalee
Shankavaram, Uma
Camphausen, Kevin
Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title_full Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title_fullStr Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title_full_unstemmed Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title_short Correlation of Plasma FL Expression with Bone Marrow Irradiation Dose
title_sort correlation of plasma fl expression with bone marrow irradiation dose
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591371/
https://www.ncbi.nlm.nih.gov/pubmed/23505536
http://dx.doi.org/10.1371/journal.pone.0058558
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