Literature DB >> 26198166

Cell Therapy Using Human Induced Pluripotent Stem Cell-Derived Renal Progenitors Ameliorates Acute Kidney Injury in Mice.

Takafumi Toyohara1, Shin-Ichi Mae1, Shin-Ichi Sueta1, Tatsuyuki Inoue1, Yukiko Yamagishi1, Tatsuya Kawamoto1, Tomoko Kasahara1, Azusa Hoshina1, Taro Toyoda1, Hiromi Tanaka1, Toshikazu Araoka1, Aiko Sato-Otsubo1, Kazutoshi Takahashi1, Yasunori Sato1, Noboru Yamaji1, Seishi Ogawa1, Shinya Yamanaka1, Kenji Osafune2.   

Abstract

UNLABELLED: Acute kidney injury (AKI) is defined as a rapid loss of renal function resulting from various etiologies, with a mortality rate exceeding 60% among intensive care patients. Because conventional treatments have failed to alleviate this condition, the development of regenerative therapies using human induced pluripotent stem cells (hiPSCs) presents a promising new therapeutic option for AKI. We describe our methodology for generating renal progenitors from hiPSCs that show potential in ameliorating AKI. We established a multistep differentiation protocol for inducing hiPSCs into OSR1+SIX2+ renal progenitors capable of reconstituting three-dimensional proximal renal tubule-like structures in vitro and in vivo. Moreover, we found that renal subcapsular transplantation of hiPSC-derived renal progenitors ameliorated the AKI in mice induced by ischemia/reperfusion injury, significantly suppressing the elevation of blood urea nitrogen and serum creatinine levels and attenuating histopathological changes, such as tubular necrosis, tubule dilatation with casts, and interstitial fibrosis. To our knowledge, few reports demonstrating the therapeutic efficacy of cell therapy with renal lineage cells generated from hiPSCs have been published. Our results suggest that regenerative medicine strategies for kidney diseases could be developed using hiPSC-derived renal cells. SIGNIFICANCE: This report is the first to demonstrate that the transplantation of renal progenitor cells differentiated from human induced pluripotent stem (iPS) cells has therapeutic effectiveness in mouse models of acute kidney injury induced by ischemia/reperfusion injury. In addition, this report clearly demonstrates that the therapeutic benefits come from trophic effects by the renal progenitor cells, and it identifies the renoprotective factors secreted by the progenitors. The results of this study indicate the feasibility of developing regenerative medicine strategy using iPS cells against renal diseases. ©AlphaMed Press.

Entities:  

Keywords:  Acute kidney injury; Cell- and tissue-based therapy; Induced pluripotent stem cells; Kidney; Nephrons; Renal progenitors; SIX2 protein

Mesh:

Substances:

Year:  2015        PMID: 26198166      PMCID: PMC4542865          DOI: 10.5966/sctm.2014-0219

Source DB:  PubMed          Journal:  Stem Cells Transl Med        ISSN: 2157-6564            Impact factor:   6.940


  52 in total

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