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HERO ID
3045470
Reference Type
Journal Article
Title
Influence of Di(2-ethylhexyl)phthalate on migration rate and differentiation of human hematopoietic stem and progenitor cells (CD34+)
Author(s)
Manz, P; Cadeddu, RP; Wilk, M; Fischer, JC; Fritz, B; Haas, R; Wenzel, F
Year
2015
Is Peer Reviewed?
1
Journal
Clinical Hemorheology and Microcirculation
ISSN:
1386-0291
EISSN:
1875-8622
Publisher
IOS Press
Volume
61
Issue
2
Page Numbers
111-118
Language
English
PMID
26410866
DOI
10.3233/CH-151984
Web of Science Id
WOS:000364596000001
URL
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84946722287&doi=10.3233%2fCH-151984&partnerID=40&md5=126d7bb878fc03a87ebb94e8ab476c88
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Relationship(s)
is related to other part(s)
3230529
Influence of Di(2-ethylhexyl)phthalate on migration rate and differentiation of human hematopoietic stem and progenitor Cells (CD34+)
Abstract
INTRODUCTION:
Phthalates are a group of synthetic plasticizers that are ubiquitous environmental pollutants with toxic and endocrine disrupting characteristics. DEHP is the most commonly used plasticizer in the world and is still applied to stem cell transfusion bags used for storage of hematopoietic stem and progenitor cells (CD34+ HSPC), which are transferred during stem cell transplantation. Here we examined the effect of DEHP on vitality of CD34+ HSPC as well as stem cell specific properties like migration and differentiation capacity - both important for successful stem cell transplantations.
MATERIAL AND METHODS:
CD34+ HSPC were incubated for 24 h and 72 h with DEHP concentrations ranging from 1 μg/ml to 250 μg/ml. DEHP was diluted in DMSO. Migration rate was analyzed along an SDF-1α gradient using Transwell migration inserts. Differentiation of CD34+ HSPC was investigated after two weeks in methylcellulose with colony stimulating factors. Apoptosis rate was measured via Annexin V and 7-AAD staining.
RESULTS:
24 h of incubation with 10 μg/ml DEHP led to a significant (p < 0.01) decrease in migration rate of CD34+ HSPC (70.70% ± 7.53% ) with a minimum migration rate of 48.33% ± 6.72% in relation to control after incubation with 100 μg/ml DEHP for 72 h. Incubation with the highest tested DEHP concentrations (50 and 100 μg/ml) significantly (p < 0.05) altered colony formation rate and cell type distribution. Apoptosis rate of CD34+ HSPC significantly (p < 0.05) increased after incubation with concentrations of 10 μg/ml DEHP for 24 h (1.46 ± 0.19) with a maximum apoptosis rate of 2.71 ± 0.66 after 24 h incubation with the highest DEHP concentration (250 μg/ml) in relation to control.
CONCLUSIONS:
As shown, DEHP takes impact on migration rate, apoptosis rate, and differentiation of CD34+ HSPC. As these are functions with an important role in stem cell transplantations, the usage of DEHP-free stem cell transfusion bags should be considered.
Keywords
Phthalates; DEHP; hematopoietic stem cells; CD34(+); vitality; migration; differentiation; apoptosis; apheresis; stem cell transplantation
Tags
IRIS
•
Dibutyl Phthalate (DBP)
Database Searches
LitSearch Jul 2016 - Jan 2017
Prior search overlap
WoS
Excluded: No Primary Data on Health Effects
Not chemical specific
Use in sample prep or assay
Litsearch June 2015 - Jan 2016
Pubmed
Web of Science
•
Phthalates – Targeted Search for Epidemiological Studies
Source – all searches
Pubmed
WOS
Excluded
Source – Dec 2015 Update (Private)
Pubmed
Source - Jun 2016 Update (Private)
WOS
Source - Dec 2016 Update (Private)
Pubmed
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