Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cells
Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor organs in the future. This approach has been tested in rats, and has been partially explored in porcine and human lungs. However, existing bioenginee...
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Published in: | Scientific reports Vol. 7; no. 1; pp. 8447 - 15 |
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Abstract | Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor organs in the future. This approach has been tested in rats, and has been partially explored in porcine and human lungs. However, existing bioengineered lungs are fragile, in part because of their immature vascular structure. Herein, we report the application of adipose-derived stem/stromal cells (ASCs) for engineering the pulmonary vasculature in a decellularized rat lung scaffold. We found that pre-seeded ASCs differentiated into pericytes and stabilized the endothelial cell (EC) monolayer in nascent pulmonary vessels, thereby contributing to EC survival in the regenerated lungs. The ASC-mediated stabilization of the ECs clearly reduced vascular permeability and suppressed alveolar hemorrhage in an orthotopic transplant model for up to 3 h after extubation. Fibroblast growth factor 9, a mesenchyme-targeting growth factor, enhanced ASC differentiation into pericytes but overstimulated their proliferation, causing a partial obstruction of the vasculature in the regenerated lung. ASCs may therefore provide a promising cell source for vascular regeneration in bioengineered lungs, though additional work is needed to optimize the growth factor or hormone milieu for organ culture. |
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AbstractList | Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor organs in the future. This approach has been tested in rats, and has been partially explored in porcine and human lungs. However, existing bioengineered lungs are fragile, in part because of their immature vascular structure. Herein, we report the application of adipose-derived stem/stromal cells (ASCs) for engineering the pulmonary vasculature in a decellularized rat lung scaffold. We found that pre-seeded ASCs differentiated into pericytes and stabilized the endothelial cell (EC) monolayer in nascent pulmonary vessels, thereby contributing to EC survival in the regenerated lungs. The ASC-mediated stabilization of the ECs clearly reduced vascular permeability and suppressed alveolar hemorrhage in an orthotopic transplant model for up to 3 h after extubation. Fibroblast growth factor 9, a mesenchyme-targeting growth factor, enhanced ASC differentiation into pericytes but overstimulated their proliferation, causing a partial obstruction of the vasculature in the regenerated lung. ASCs may therefore provide a promising cell source for vascular regeneration in bioengineered lungs, though additional work is needed to optimize the growth factor or hormone milieu for organ culture. Abstract Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor organs in the future. This approach has been tested in rats, and has been partially explored in porcine and human lungs. However, existing bioengineered lungs are fragile, in part because of their immature vascular structure. Herein, we report the application of adipose-derived stem/stromal cells (ASCs) for engineering the pulmonary vasculature in a decellularized rat lung scaffold. We found that pre-seeded ASCs differentiated into pericytes and stabilized the endothelial cell (EC) monolayer in nascent pulmonary vessels, thereby contributing to EC survival in the regenerated lungs. The ASC-mediated stabilization of the ECs clearly reduced vascular permeability and suppressed alveolar hemorrhage in an orthotopic transplant model for up to 3 h after extubation. Fibroblast growth factor 9, a mesenchyme-targeting growth factor, enhanced ASC differentiation into pericytes but overstimulated their proliferation, causing a partial obstruction of the vasculature in the regenerated lung. ASCs may therefore provide a promising cell source for vascular regeneration in bioengineered lungs, though additional work is needed to optimize the growth factor or hormone milieu for organ culture. |
ArticleNumber | 8447 |
Author | Ogi, Tomoo Sengyoku, Hideyori Matsumoto, Keitaro Matsuu-Matsuyama, Mutsumi Yukawa, Hiroshi Tsuchiya, Tomoshi Mitsutake, Norisato Akita, Sadanori Hatachi, Go Niklason, Laura E. Obata, Tomohiro Nagayasu, Takeshi Watanabe, Hironosuke Nishimura, Satoshi Miyazaki, Takuro Kamohara, Ryotaro Nakazawa, Yuka Baba, Yoshinobu Yamasaki, Naoya Doi, Ryoichiro |
Author_xml | – sequence: 1 givenname: Ryoichiro surname: Doi fullname: Doi, Ryoichiro organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 2 givenname: Tomoshi surname: Tsuchiya fullname: Tsuchiya, Tomoshi email: tomoshi@nagasaki-u.ac.jp organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Translational Research Center, Research Institute for Science & Technology, Tokyo University of Science – sequence: 3 givenname: Norisato orcidid: 0000-0002-2744-8046 surname: Mitsutake fullname: Mitsutake, Norisato organization: Department of Radiation Medical Sciences, Atomic Bomb Disease Institute, Nagasaki University – sequence: 4 givenname: Satoshi surname: Nishimura fullname: Nishimura, Satoshi organization: Department of Cardiovascular Medicine, Translational Systems Biology and Medicine Initiative, Graduate School of Medicine, The University of Tokyo, Center for Molecular Medicine, Jichi Medical University – sequence: 5 givenname: Mutsumi orcidid: 0000-0003-2106-4436 surname: Matsuu-Matsuyama fullname: Matsuu-Matsuyama, Mutsumi organization: Department of Tumor and Diagnostic Pathology, Atomic Bomb Disease Institute, Nagasaki University – sequence: 6 givenname: Yuka surname: Nakazawa fullname: Nakazawa, Yuka organization: Department of Genome Repair, Atomic Bomb Disease Institute, Nagasaki University – sequence: 7 givenname: Tomoo surname: Ogi fullname: Ogi, Tomoo organization: Department of Genetics, Research Institute of Environmental Medicine, Nagoya University – sequence: 8 givenname: Sadanori surname: Akita fullname: Akita, Sadanori organization: Department of Plastic Surgery, Wound Repair and Regeneration, Fukuoka University – sequence: 9 givenname: Hiroshi surname: Yukawa fullname: Yukawa, Hiroshi organization: FIRST Research Center for Innovative Nanobiodevices, Graduate School of Engineering, Nagoya University – sequence: 10 givenname: Yoshinobu surname: Baba fullname: Baba, Yoshinobu organization: FIRST Research Center for Innovative Nanobiodevices, Graduate School of Engineering, Nagoya University – sequence: 11 givenname: Naoya surname: Yamasaki fullname: Yamasaki, Naoya organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Medical-Engineering Hybrid Professional Development Center, Nagasaki University Graduate School of Biomedical Sciences – sequence: 12 givenname: Keitaro surname: Matsumoto fullname: Matsumoto, Keitaro organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Medical-Engineering Hybrid Professional Development Center, Nagasaki University Graduate School of Biomedical Sciences – sequence: 13 givenname: Takuro surname: Miyazaki fullname: Miyazaki, Takuro organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 14 givenname: Ryotaro surname: Kamohara fullname: Kamohara, Ryotaro organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 15 givenname: Go surname: Hatachi fullname: Hatachi, Go organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 16 givenname: Hideyori surname: Sengyoku fullname: Sengyoku, Hideyori organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 17 givenname: Hironosuke surname: Watanabe fullname: Watanabe, Hironosuke organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 18 givenname: Tomohiro surname: Obata fullname: Obata, Tomohiro organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences – sequence: 19 givenname: Laura E. surname: Niklason fullname: Niklason, Laura E. organization: Department of Biomedical Engineering, Yale University, Department of Anesthesia, Yale University – sequence: 20 givenname: Takeshi surname: Nagayasu fullname: Nagayasu, Takeshi email: nagayasu@nagasaki-u.ac.jp organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Medical-Engineering Hybrid Professional Development Center, Nagasaki University Graduate School of Biomedical Sciences |
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Snippet | Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor organs... Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient's own cells could provide desperately needed donor organs... Abstract Bioengineered lungs consisting of a decellularized lung scaffold that is repopulated with a patient’s own cells could provide desperately needed donor... |
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Title | Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cells |
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