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Longitudinal monitoring adipose-derived stem cell survival by PET imaging hexadecyl-4-I-124-iodobenzoate in rat myocardial infarction model

Authors
Kim, Min HwanWoo, Sang-KeunLee, Kyo ChulAn, Gwang IlPandya, DarpanPark, Noh WonNahm, Sang-SoepEom, Ki DongKim, Kwang IlLee, Tae SupKim, Chan WhaKang, Joo HyunYoo, JeongsooLee, Yong Jin
Issue Date
2-Jan-2015
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Adipose-derived stem cells; Cell tracking; Direct labeling agent; Hexadecyl-4-I-124-iodobenzoate; Myocardial infarction
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.456, no.1, pp.13 - 19
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
456
Number
1
Start Page
13
End Page
19
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/94668
DOI
10.1016/j.bbrc.2014.11.019
ISSN
0006-291X
Abstract
This study aims to monitor how the change of cell survival of transplanted adipose-derived stem cells (ADSCs) responds to myocardial infarction (MI) via the hexadecyl-4-I-124-iodobenzoate (I-124-HIB) mediated direct labeling method in vivo. Stem cells have shown the potential to improve cardiac function after MI. However, monitoring of the fate of transplanted stem cells at target sites is still unclear. Rat ADSCs were labeled with I-124-HIB, and radiolabeled ADSCs were transplanted into the myocardium of normal and MI model. In the group of I-124-HIB-labeled ADSC transplantation, in vivo imaging was performed using small-animal positron emission tomography (PET)/computed tomography (CT) for 9 days. Twenty-one days post-transplantation, histopathological analysis and apoptosis assay were performed. ADSC viability and differentiation were not affected by I-124-HIB labeling. In vivo tracking of the I-124-HIB-labeled ADSCs was possible for 9 and 3 days in normal and MI model, respectively. Apoptosis of transplanted cells increased in the MI model compared than that in normal model. We developed a direct labeling agent, I-124-HIB, and first tried to longitudinally monitor transplanted stem cell to MI. This approach may provide new insights on the roles of stem cell monitoring in living bodies for stem cell therapy from pre-clinical studies to clinical trials. (C) 2014 Elsevier Inc. All rights reserved.
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