TY - JOUR
T1 - Generation of induced nephron progenitor-like cells from human urine-derived cells
AU - Gao, Wei Wei
AU - Zheng, Jie
AU - Yun, Wonjin
AU - Kang, Phil Jun
AU - Park, Gyuman
AU - Song, Gwonhwa
AU - Kim, In Yong
AU - You, Seungkwon
N1 - Funding Information:
Funding: This work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Korean government (MSIT) 2014M3A9D3034158, 2014M3A9D3034164, 2016R1C1B1011180, 2018R1C1B5040264, 2019R1A2C1004046, 2019R1F1A1044473, and 2019R1H1A1079839, and by the Ministry of Trade, Industry, and Energy (R0005886). This work was also supported by the School of Life Sciences and Biotechnology for BK21 PLUS, Korea University, and STEMLAB, Inc.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - Background: Regenerative medicine strategies employing nephron progenitor cells (NPCs) are a viable approach that is worthy of substantial consideration as a promising cell source for kidney diseases. However, the generation of induced nephron progenitor-like cells (iNPCs) from human somatic cells remains a major challenge. Here, we describe a novel method for generating NPCs from human urine-derived cells (UCs) that can undergo long-term expansion in a serum-free condition. Results: Here, we generated iNPCs from human urine-derived cells by forced expression of the transcription factors OCT4, SOX2, KLF4, c-MYC, and SLUG, followed by exposure to a cocktail of defined small molecules. These iNPCs resembled human embryonic stem cell-derived NPCs in terms of their morphology, biological characteristics, differentiation potential, and global gene expression and underwent a long-term expansion in serum-free conditions. Conclusion: This study demonstrates that human iNPCs can be readily generated and expanded, which will facilitate their broad applicability in a rapid, efficient, and patient-specific manner, particularly holding the potential as a transplantable cell source for patients with kidney disease.
AB - Background: Regenerative medicine strategies employing nephron progenitor cells (NPCs) are a viable approach that is worthy of substantial consideration as a promising cell source for kidney diseases. However, the generation of induced nephron progenitor-like cells (iNPCs) from human somatic cells remains a major challenge. Here, we describe a novel method for generating NPCs from human urine-derived cells (UCs) that can undergo long-term expansion in a serum-free condition. Results: Here, we generated iNPCs from human urine-derived cells by forced expression of the transcription factors OCT4, SOX2, KLF4, c-MYC, and SLUG, followed by exposure to a cocktail of defined small molecules. These iNPCs resembled human embryonic stem cell-derived NPCs in terms of their morphology, biological characteristics, differentiation potential, and global gene expression and underwent a long-term expansion in serum-free conditions. Conclusion: This study demonstrates that human iNPCs can be readily generated and expanded, which will facilitate their broad applicability in a rapid, efficient, and patient-specific manner, particularly holding the potential as a transplantable cell source for patients with kidney disease.
KW - Direct reprogramming
KW - Kidney
KW - Nephron progenitor cells
KW - Transdifferentiation
KW - Urine cells
UR - http://www.scopus.com/inward/record.url?scp=85121050033&partnerID=8YFLogxK
U2 - 10.3390/ijms222413449
DO - 10.3390/ijms222413449
M3 - Article
C2 - 34948246
AN - SCOPUS:85121050033
SN - 1661-6596
VL - 22
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 24
M1 - 13449
ER -