| Literature DB >> 33467726 |
Sungho Shin1,2, Jeongmin Lee3,4, Yumi Kwon1, Kang-Sik Park2,5, Jae-Hoon Jeong6, Suk-Joo Choi7, Sa Ik Bang8, Jong Wook Chang3,4, Cheolju Lee1,2,9.
Abstract
Mesenchymal stem cells (MSCs) have the potential to be a viable therapy against various diseases due to their paracrine effects, such as secretion of immunomodulatory, trophic and protective factors. These cells are known to be distributed within various organs and tissues. Although they possess the same characteristics, MSCs from different sources are believed to have different secretion potentials and patterns, which may influence their therapeutic effects in disease environments. We characterized the protein secretome of adipose (AD), bone marrow (BM), placenta (PL), and Wharton's jelly (WJ)-derived human MSCs by using conditioned media and analyzing the secretome by mass spectrometry and follow-up bioinformatics. Each MSC secretome profile had distinct characteristics depending on the source. However, the functional analyses of the secretome from different sources showed that they share similar characteristics, such as cell migration and negative regulation of programmed cell death, even though differences in the composition of the secretome exist. This study shows that the secretome of fetal-derived MSCs, such as PL and WJ, had a more diverse composition than that of AD and BM-derived MSCs, and it was assumed that their therapeutic potential was greater because of these properties.Entities:
Keywords: Wharton’s jelly; adipose; bone marrow; mass spectrometry; mesenchymal stem cells; placenta; secretome
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Year: 2021 PMID: 33467726 PMCID: PMC7829982 DOI: 10.3390/ijms22020845
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923