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Human umbilical cord-derived mesenchymal stem cells in acute liver injury: Hepatoprotective efficacy, subchronic toxicity, tumorigenicity, and biodistribution

Authors
Yun, Jun-WonAhn, Jae HunKwon, EunaKim, Seung-HyunKim, HannaJang, Ja-JuneKim, Woo HoKim, Ji HyangHan, Su-youneKim, Jin TacKim, Jong-HoonKim, WookhwanKu, Seung-YupDo, Byung-RokKang, Byeong-Cheol
Issue Date
11월-2016
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Umbilical cord-derived mesenchymal stem cells; Liver injury; Toxicity; Tumorigenicity; Biodistribution
Citation
REGULATORY TOXICOLOGY AND PHARMACOLOGY, v.81, pp.437 - 447
Indexed
SCIE
SCOPUS
Journal Title
REGULATORY TOXICOLOGY AND PHARMACOLOGY
Volume
81
Start Page
437
End Page
447
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86955
DOI
10.1016/j.yrtph.2016.09.029
ISSN
0273-2300
Abstract
Umbilical cord-derived mesenchymal stem cells (UC-MSCs) therapy might be an alternative to liver transplantation for acute or chronic liver injury. The aim of this study was to evaluate the efficacy of human UC-MSCs on carbon tetrachloride (CCl4)-induced acute liver injury. In addition, its toxicity, tumorigenicity, and biodistribution were determined. Significant hepatoprotective effects of hUC-MSCs with decreased levels of hepatocellular necrosis and lobular neutrophilic infiltration were found. Regarding the safety of hUC-MSCs, no serious hUC-MSCs-related changes (body weight, food/water consumption, clinical symptom, urinalysis, hematology, clinical chemistry, organ weight, and histopathology) were observed in a 13-week subchronic toxicity study. In a 26-week tumorigenicity study, no mice developed tumor related to hUC-MSCs transplantation up to 1 x 10(8) cells/kg. In particular, human mitochondrial sequence detection revealed that most hUC-MSCs were cleared from the major organs of the mice at 13 weeks after transplantation. There was no systemic toxicity or neoplastic finding either. Taken together, these results suggested that hUC-MSCs have great potential for future clinical treatment of acute liver disease. (C) 2016 Elsevier Inc. All rights reserved.
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