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
Main Authors: Doi, Ryoichiro, Tsuchiya, Tomoshi, Mitsutake, Norisato, Nishimura, Satoshi, Matsuu-Matsuyama, Mutsumi, Nakazawa, Yuka, Ogi, Tomoo, Akita, Sadanori, Yukawa, Hiroshi, Baba, Yoshinobu, Yamasaki, Naoya, Matsumoto, Keitaro, Miyazaki, Takuro, Kamohara, Ryotaro, Hatachi, Go, Sengyoku, Hideyori, Watanabe, Hironosuke, Obata, Tomohiro, Niklason, Laura E., Nagayasu, Takeshi
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 16-08-2017
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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.
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
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  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Translational Research Center, Research Institute for Science & Technology, Tokyo University of Science
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  orcidid: 0000-0002-2744-8046
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  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
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  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
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  givenname: Yuka
  surname: Nakazawa
  fullname: Nakazawa, Yuka
  organization: Department of Genome Repair, Atomic Bomb Disease Institute, Nagasaki University
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  givenname: Tomoo
  surname: Ogi
  fullname: Ogi, Tomoo
  organization: Department of Genetics, Research Institute of Environmental Medicine, Nagoya University
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  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
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  givenname: Takuro
  surname: Miyazaki
  fullname: Miyazaki, Takuro
  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Ryotaro
  surname: Kamohara
  fullname: Kamohara, Ryotaro
  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Go
  surname: Hatachi
  fullname: Hatachi, Go
  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Hideyori
  surname: Sengyoku
  fullname: Sengyoku, Hideyori
  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Hironosuke
  surname: Watanabe
  fullname: Watanabe, Hironosuke
  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Tomohiro
  surname: Obata
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  organization: Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences
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  givenname: Laura E.
  surname: Niklason
  fullname: Niklason, Laura E.
  organization: Department of Biomedical Engineering, Yale University, Department of Anesthesia, Yale University
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  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
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28814761$$D View this record in MEDLINE/PubMed
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  ident: 9115_CR35
  publication-title: J Thorac Cardiovasc Surg
  doi: 10.1016/S0022-5223(19)34549-0
  contributor:
    fullname: T Mizuta
SSID ssj0000529419
Score 2.4840884
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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13/109
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13/51
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Adipocytes - cytology
Adipocytes - metabolism
Alveoli
Animals
Bioengineering - methods
Cell culture
Cell Differentiation
Cell Proliferation
Cells, Cultured
Endothelial cells
Endothelial Cells - cytology
Endothelial Cells - metabolism
Extubation
Fibroblast growth factor 9
Growth factors
HEK293 Cells
Hemorrhage
Humanities and Social Sciences
Humans
Lung - blood supply
Lung - cytology
Lung - physiology
Lung Transplantation - methods
Lungs
Male
Mesenchyme
multidisciplinary
Organ culture
Pericytes
Pericytes - cytology
Pericytes - metabolism
Permeability
Pulmonary Artery - cytology
Rats, Inbred F344
Regeneration
Rodents
Science
Science (multidisciplinary)
Stromal cells
Stromal Cells - cytology
Stromal Cells - metabolism
Swine
Transplantation
Transplants & implants
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Title Transplantation of bioengineered rat lungs recellularized with endothelial and adipose-derived stromal cells
URI https://link.springer.com/article/10.1038/s41598-017-09115-2
https://www.ncbi.nlm.nih.gov/pubmed/28814761
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Volume 7
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