Title The Higher Inherent Therapeutic Potential of Biomaterial-Based hDPSCs and hEnSCs for Pancreas Diseases
Authors Xu, Bingbing
Yuan, Fu-Zhen
Lin, Lin
Ye, Jing
Fan, Bao-Shi
Zhang, Ji-Ying
Yang, Meng
Jiang, Dong
Jiang, Wen-Bo
Wang, Xing
Yu, Jia-Kuo
Affiliation Peking Univ, Hosp 3, Knee Surg Dept, Inst Spots Med, Beijing, Peoples R China
Weifang Med Univ, Sch Clin Med, Weifang, Peoples R China
Shanghai Jiao Tong Univ, Sch Med, Clin Translat R&D Ctr 3D Printing Technol, Shanghai Peoples Hosp 9, Shanghai, Peoples R China
Chinese Acad Sci, Beijing Natl Lab Mol Sci, State Key Lab Polymer Phys & Chem, Inst Chem, Beijing, Peoples R China
Univ Chinese Acad Sci, Beijing, Peoples R China
Keywords MESENCHYMAL STEM-CELLS
BETA-CELLS
ADIPOSE-TISSUE
IN-VITRO
DIFFERENTIATION
GENERATION
INSULIN
MODEL
Issue Date 26-Jun-2020
Publisher FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY
Abstract Human endometrial stem cells (hEnSCs), dental pulp stem cells (hDPSCs) and adipose tissue-derived stem cells (hADSCs) are considered to be the promising candidates for the treatment of pancreas diseases. The prognosis is better within situinjection of mesenchymal stem cells (MSCs) to the damaged pancreas compared with intravenous injection. However, the clinical application of these cells are limited, due to poor engraftment of transplanted cells after delivery. On the other hand, understanding the role of the biomaterials in cell therapy is essential to promote the therapeutic effects of MSCs. Matrigel, a basement membrane matrix biomaterial, is rich in laminin and collagen IV. The aim of this study is to investigate the difference of biological characteristics of hEnSCs, hDPSCs and hADSCsin vitroand their survival situation with Matrigel post intrapancreatic transplantationin vivo. Our findings showed, firstly, there was no significant difference in morphology and immunophenotype of these MSCs. Secondly, the biological properties, including cell proliferation, the ability of adipogenic and osteogenic differentiation and the mRNA expression levels of pancreas development-related genes, have been showed distinct difference among these MSCs. Thirdly, Matrigel can improve the survival of MSCsin vivo, especially for Matrigel-based hDPSCs and Matrigel-based hEnSCs in pancreas parenchyma of SD rats. These results suggest that hDPSCs and hEnSCs are with the greater inherent therapeutic potential for pancreas diseases compared with hADSCs.
URI http://hdl.handle.net/20.500.11897/590512
ISSN 2296-4185
DOI 10.3389/fbioe.2020.00636
Indexed SCI(E)
Appears in Collections: 第三医院

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