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Improved Isolation and Culture of Urine-Derived Stem Cells (USCs) and Enhanced Production of Immune Cells from the USC-Derived Induced Pluripotent Stem Cells

Overview
Journal J Clin Med
Specialty General Medicine
Date 2020 Mar 22
PMID 32197458
Citations 15
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Abstract

The availability of autologous adult stem cells is one of the essential prerequisites for human stem cell therapy. Urine-derived stem cells (USCs) are considered as desirable cell sources for cell therapy because donor-specific USCs are easily and non-invasively obtained from urine. Efficient isolation, expansion, and differentiation methods of USCs are necessary to increase their availability. Here, we developed a method for efficient isolation and expansion of USCs using Matrigel, and the rho-associated protein kinase (ROCK) inhibitor, Y-27632. The prepared USCs showed significantly enhanced migration, colony forming capacity, and differentiation into osteogenic or chondrogenic lineage. The USCs were successfully reprogramed into induced pluripotent stem cells (USC-iPSCs) and further differentiated into kidney organoid and hematopoietic progenitor cells (HPCs). Using flavonoid molecules, the isolation efficiency of USCs and the production of HPCs from the USC-iPSCs was increased. Taken together, we present an improved isolation method of USCs utilizing Matrigel, a ROCK inhibitor and flavonoids, and enhanced differentiation of USC-iPSC to HPC by flavonoids. These novel findings could significantly enhance the use of USCs and USC-iPSCs for stem cell research and further application in regenerative stem cell-based therapies.

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References
1.
Kang H, Choi S, Kim B, Choi J, Park G, Kwon T . Advanced Properties of Urine Derived Stem Cells Compared to Adipose Tissue Derived Stem Cells in Terms of Cell Proliferation, Immune Modulation and Multi Differentiation. J Korean Med Sci. 2015; 30(12):1764-76. PMC: 4689820. DOI: 10.3346/jkms.2015.30.12.1764. View

2.
Watanabe K, Ueno M, Kamiya D, Nishiyama A, Matsumura M, Wataya T . A ROCK inhibitor permits survival of dissociated human embryonic stem cells. Nat Biotechnol. 2007; 25(6):681-6. DOI: 10.1038/nbt1310. View

3.
Ma Y, Han X, Quintana Bustamante O, Bessa de Castro R, Zhang K, Zhang P . Highly efficient genome editing of human hematopoietic stem cells via a nano-silicon-blade delivery approach. Integr Biol (Camb). 2017; 9(6):548-554. PMC: 5598083. DOI: 10.1039/c7ib00060j. View

4.
Nakamura K, Yoshimura A, Kaneko T, Sato K, Hara Y . ROCK inhibitor Y-27632 maintains the proliferation of confluent human mesenchymal stem cells. J Periodontal Res. 2013; 49(3):363-70. DOI: 10.1111/jre.12114. View

5.
Kern S, Eichler H, Stoeve J, Kluter H, Bieback K . Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue. Stem Cells. 2006; 24(5):1294-301. DOI: 10.1634/stemcells.2005-0342. View