Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model

Introduction: Pluripotent stem cells have an advantage that they can proliferate without reduction of the quality, while they have risk of tumorigenesis. It is desirable that pluripotent stem cells can be utilized safely with minimal effort in cartilage regenerative medicine. To accomplish this, we...

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Main Authors: Sakura Uto, Satoru Nishizawa, Atsuhiko Hikita, Tsuyoshi Takato, Kazuto Hoshi
Format: Article
Language:English
Published: Elsevier 2018-12-01
Series:Regenerative Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S2352320418300105
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spelling doaj-78c6d685257147aab3e20f733f2876922020-11-24T21:13:40ZengElsevierRegenerative Therapy2352-32042018-12-0195870Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement modelSakura Uto0Satoru Nishizawa1Atsuhiko Hikita2Tsuyoshi Takato3Kazuto Hoshi4Department of Tissue Engineering, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, JapanTranslational Research Center, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, JapanDepartment of Tissue Engineering, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan; Department of Cell & Tissue Engineering (Fujisoft), Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, JapanJR Tokyo General Hospital, 2-1-3 Yoyogi, Shibuya-ku, Tokyo, 151-8528, JapanDepartment of Tissue Engineering, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan; Department of Sensory and Motor System Medicine, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan; Corresponding author. Department of Sensory and Motor System Medicine, Graduate School of Medicine, The University of Tokyo, Department of Oral-maxillofacial Surgery, Dentistry and Orthodontics, Division of Tissue Engineering, The University of Tokyo Hospital, Hongo 7-3-1, Bunkyo-ku, Tokyo, 113-0033, Japan. Fax: +81 3 5800-9891.Introduction: Pluripotent stem cells have an advantage that they can proliferate without reduction of the quality, while they have risk of tumorigenesis. It is desirable that pluripotent stem cells can be utilized safely with minimal effort in cartilage regenerative medicine. To accomplish this, we examined the potential usefulness of induced pluripotent stem cells (iPS cells) after minimal treatment via cell isolation and hydrogel embedding for cartilage regeneration using a large animal model. Methods: Porcine iPS-like cells were established from the CLAWN miniature pig. In vitro differentiation was examined for porcine iPS-like cells with minimal treatment. For the osteochondral replacement model, osteochondral defect was made in the quarters of the anteromedial sides of the proximal tibias in pigs. Porcine iPS-like cells and human iPS cells with minimal treatment were seeded on scaffold made of thermo-compression-bonded beta-TCP and poly-L-lactic acid and transplanted to the defect, and cartilage regeneration and tumorigenesis were evaluated. Results: The in vitro analysis indicated that the minimal treatment was sufficient to weaken the pluripotency of the porcine iPS-like cells, while chondrogenic differentiation did not occur in vitro. When porcine iPS-like cells were transplanted into osteochondral replacement model after minimal treatment in vitro, cartilage regeneration was observed without tumor formation. Additionally, fluorescent in situ hybridization (FISH) indicated that the chondrocytes in the regenerative cartilage originated from transplanted porcine iPS-like cells. Transplantation of human iPS cells also showed the regeneration of cartilage in miniature pigs under immunosuppressive treatment. Conclusion: Minimally-treated iPS cells will be a useful cell source for cartilage regenerative medicine. Keywords: iPS cells, Minimal treatment, Osteochondral replacement model, Cartilage regenerationhttp://www.sciencedirect.com/science/article/pii/S2352320418300105
collection DOAJ
language English
format Article
sources DOAJ
author Sakura Uto
Satoru Nishizawa
Atsuhiko Hikita
Tsuyoshi Takato
Kazuto Hoshi
spellingShingle Sakura Uto
Satoru Nishizawa
Atsuhiko Hikita
Tsuyoshi Takato
Kazuto Hoshi
Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
Regenerative Therapy
author_facet Sakura Uto
Satoru Nishizawa
Atsuhiko Hikita
Tsuyoshi Takato
Kazuto Hoshi
author_sort Sakura Uto
title Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
title_short Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
title_full Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
title_fullStr Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
title_full_unstemmed Application of induced pluripotent stem cells for cartilage regeneration in CLAWN miniature pig osteochondral replacement model
title_sort application of induced pluripotent stem cells for cartilage regeneration in clawn miniature pig osteochondral replacement model
publisher Elsevier
series Regenerative Therapy
issn 2352-3204
publishDate 2018-12-01
description Introduction: Pluripotent stem cells have an advantage that they can proliferate without reduction of the quality, while they have risk of tumorigenesis. It is desirable that pluripotent stem cells can be utilized safely with minimal effort in cartilage regenerative medicine. To accomplish this, we examined the potential usefulness of induced pluripotent stem cells (iPS cells) after minimal treatment via cell isolation and hydrogel embedding for cartilage regeneration using a large animal model. Methods: Porcine iPS-like cells were established from the CLAWN miniature pig. In vitro differentiation was examined for porcine iPS-like cells with minimal treatment. For the osteochondral replacement model, osteochondral defect was made in the quarters of the anteromedial sides of the proximal tibias in pigs. Porcine iPS-like cells and human iPS cells with minimal treatment were seeded on scaffold made of thermo-compression-bonded beta-TCP and poly-L-lactic acid and transplanted to the defect, and cartilage regeneration and tumorigenesis were evaluated. Results: The in vitro analysis indicated that the minimal treatment was sufficient to weaken the pluripotency of the porcine iPS-like cells, while chondrogenic differentiation did not occur in vitro. When porcine iPS-like cells were transplanted into osteochondral replacement model after minimal treatment in vitro, cartilage regeneration was observed without tumor formation. Additionally, fluorescent in situ hybridization (FISH) indicated that the chondrocytes in the regenerative cartilage originated from transplanted porcine iPS-like cells. Transplantation of human iPS cells also showed the regeneration of cartilage in miniature pigs under immunosuppressive treatment. Conclusion: Minimally-treated iPS cells will be a useful cell source for cartilage regenerative medicine. Keywords: iPS cells, Minimal treatment, Osteochondral replacement model, Cartilage regeneration
url http://www.sciencedirect.com/science/article/pii/S2352320418300105
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