221 453

Cited 103 times in

Systemic transplantation of human adipose tissue-derived mesenchymal stem cells for the regeneration of irradiation-induced salivary gland damage

Authors
 Jae-Yol Lim  ;  Jeong Chan Ra  ;  Il Seob Shin  ;  Yun Ho Jang  ;  Hye-Young An  ;  Jeong-Seok Choi  ;  Woo Cheol Kim  ;  Young-Mo Kim 
Citation
 PLOS ONE, Vol.8(8) : e71167, 2013 
Journal Title
PLOS ONE
Issue Date
2013
MeSH
Adipose Tissue/cytology ; Adipose Tissue/physiology* ; Animals ; Cell Differentiation ; Cell Transdifferentiation ; Coculture Techniques ; Epithelial Cells/cytology ; Epithelial Cells/physiology ; Female ; Graft Survival/physiology* ; Humans ; Injections, Intravenous ; Mesenchymal Stem Cell Transplantation* ; Mesenchymal Stromal Cells/cytology ; Mesenchymal Stromal Cells/physiology* ; Mice ; Mice, Inbred C3H ; Radiation Injuries, Experimental/pathology ; Radiation Injuries, Experimental/therapy* ; Regeneration ; Salivary Glands/pathology ; Salivary Glands/radiation effects* ; Salivation/physiology ; Transplantation, Heterologous ; X-Rays/adverse effects
Abstract
OBJECTIVES: Cell-based therapy has been reported to repair or restore damaged salivary gland (SG) tissue after irradiation. This study was aimed at determining whether systemic administration of human adipose-derived mesenchymal stem cells (hAdMSCs) can ameliorate radiation-induced SG damage.

METHODS: hAdMSCs (1 × 10(6)) were administered through a tail vein of C3H mice immediately after local irradiation, and then this infusion was repeated once a week for 3 consecutive weeks. At 12 weeks after irradiation, functional evaluations were conducted by measuring salivary flow rates (SFRs) and salivation lag times, and histopathologic and immunofluorescence histochemistry studies were performed to assay microstructural changes, apoptosis, and proliferation indices. The engraftment and in vivo differentiation of infused hAdMSCs were also investigated, and the transdifferentiation of hAdMSCs into amylase-producing SG epithelial cells (SGCs) was observed in vitro using a co-culture system.

RESULTS: The systemic administration of hAdMSCs exhibited improved SFRs at 12 weeks after irradiation. hAdMSC-transplanted SGs showed fewer damaged and atrophied acinar cells and higher mucin and amylase production levels than untreated irradiated SGs. Immunofluorescence TUNEL assays revealed fewer apoptotic cells in the hAdMSC group than in the untreated group. Infused hAdMSCs were detected in transplanted SGs at 4 weeks after irradiation and some cells were found to have differentiated into SGCs. In vitro, a low number of co-cultured hAdMSCs (13%-18%) were observed to transdifferentiate into SGCs.

CONCLUSION: The findings of this study indicate that hAdMSCs have the potential to protect against irradiation-induced cell loss and to transdifferentiate into SGCs, and suggest that hAdMSC administration should be viewed as a candidate therapy for the treatment of radiation-induced SG damage.
Files in This Item:
T201306340.pdf Download
DOI
10.1371/journal.pone.0071167
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
Yonsei Authors
Lim, Jae Yol(임재열) ORCID logo https://orcid.org/0000-0002-9757-6414
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/158539
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links