author_facet Samuel, Rekha
Daheron, Laurence
Liao, Shan
Vardam, Trupti
Kamoun, Walid S.
Batista, Ana
Buecker, Christa
Schäfer, Richard
Han, Xiaoxing
Au, Patrick
Scadden, David T.
Duda, Dan G.
Fukumura, Dai
Jain, Rakesh K.
Samuel, Rekha
Daheron, Laurence
Liao, Shan
Vardam, Trupti
Kamoun, Walid S.
Batista, Ana
Buecker, Christa
Schäfer, Richard
Han, Xiaoxing
Au, Patrick
Scadden, David T.
Duda, Dan G.
Fukumura, Dai
Jain, Rakesh K.
author Samuel, Rekha
Daheron, Laurence
Liao, Shan
Vardam, Trupti
Kamoun, Walid S.
Batista, Ana
Buecker, Christa
Schäfer, Richard
Han, Xiaoxing
Au, Patrick
Scadden, David T.
Duda, Dan G.
Fukumura, Dai
Jain, Rakesh K.
spellingShingle Samuel, Rekha
Daheron, Laurence
Liao, Shan
Vardam, Trupti
Kamoun, Walid S.
Batista, Ana
Buecker, Christa
Schäfer, Richard
Han, Xiaoxing
Au, Patrick
Scadden, David T.
Duda, Dan G.
Fukumura, Dai
Jain, Rakesh K.
Proceedings of the National Academy of Sciences
Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
Multidisciplinary
author_sort samuel, rekha
spelling Samuel, Rekha Daheron, Laurence Liao, Shan Vardam, Trupti Kamoun, Walid S. Batista, Ana Buecker, Christa Schäfer, Richard Han, Xiaoxing Au, Patrick Scadden, David T. Duda, Dan G. Fukumura, Dai Jain, Rakesh K. 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.1310675110 <jats:p>Efficient generation of competent vasculogenic cells is a critical challenge of human induced pluripotent stem (hiPS) cell-based regenerative medicine. Biologically relevant systems to assess functionality of the engineered vessels in vivo are equally important for such development. Here, we report a unique approach for the derivation of endothelial precursor cells from hiPS cells using a triple combination of selection markers—CD34, neuropilin 1, and human kinase insert domain-containing receptor—and an efficient 2D culture system for hiPS cell-derived endothelial precursor cell expansion. With these methods, we successfully generated endothelial cells (ECs) from hiPS cells obtained from healthy donors and formed stable functional blood vessels in vivo, lasting for 280 d in mice. In addition, we developed an approach to generate mesenchymal precursor cells (MPCs) from hiPS cells in parallel. Moreover, we successfully generated functional blood vessels in vivo using these ECs and MPCs derived from the same hiPS cell line. These data provide proof of the principle that autologous hiPS cell-derived vascular precursors can be used for in vivo applications, once safety and immunological issues of hiPS-based cellular therapy have been resolved. Additionally, the durability of hiPS-derived blood vessels in vivo demonstrates a potential translation of this approach in long-term vascularization for tissue engineering and treatment of vascular diseases. Of note, we have also successfully generated ECs and MPCs from type 1 diabetic patient-derived hiPS cell lines and use them to generate blood vessels in vivo, which is an important milestone toward clinical translation of this approach.</jats:p> Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells Proceedings of the National Academy of Sciences
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title Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_unstemmed Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_full Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_fullStr Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_full_unstemmed Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_short Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_sort generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.1310675110
publishDate 2013
physical 12774-12779
description <jats:p>Efficient generation of competent vasculogenic cells is a critical challenge of human induced pluripotent stem (hiPS) cell-based regenerative medicine. Biologically relevant systems to assess functionality of the engineered vessels in vivo are equally important for such development. Here, we report a unique approach for the derivation of endothelial precursor cells from hiPS cells using a triple combination of selection markers—CD34, neuropilin 1, and human kinase insert domain-containing receptor—and an efficient 2D culture system for hiPS cell-derived endothelial precursor cell expansion. With these methods, we successfully generated endothelial cells (ECs) from hiPS cells obtained from healthy donors and formed stable functional blood vessels in vivo, lasting for 280 d in mice. In addition, we developed an approach to generate mesenchymal precursor cells (MPCs) from hiPS cells in parallel. Moreover, we successfully generated functional blood vessels in vivo using these ECs and MPCs derived from the same hiPS cell line. These data provide proof of the principle that autologous hiPS cell-derived vascular precursors can be used for in vivo applications, once safety and immunological issues of hiPS-based cellular therapy have been resolved. Additionally, the durability of hiPS-derived blood vessels in vivo demonstrates a potential translation of this approach in long-term vascularization for tissue engineering and treatment of vascular diseases. Of note, we have also successfully generated ECs and MPCs from type 1 diabetic patient-derived hiPS cell lines and use them to generate blood vessels in vivo, which is an important milestone toward clinical translation of this approach.</jats:p>
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author Samuel, Rekha, Daheron, Laurence, Liao, Shan, Vardam, Trupti, Kamoun, Walid S., Batista, Ana, Buecker, Christa, Schäfer, Richard, Han, Xiaoxing, Au, Patrick, Scadden, David T., Duda, Dan G., Fukumura, Dai, Jain, Rakesh K.
author_facet Samuel, Rekha, Daheron, Laurence, Liao, Shan, Vardam, Trupti, Kamoun, Walid S., Batista, Ana, Buecker, Christa, Schäfer, Richard, Han, Xiaoxing, Au, Patrick, Scadden, David T., Duda, Dan G., Fukumura, Dai, Jain, Rakesh K., Samuel, Rekha, Daheron, Laurence, Liao, Shan, Vardam, Trupti, Kamoun, Walid S., Batista, Ana, Buecker, Christa, Schäfer, Richard, Han, Xiaoxing, Au, Patrick, Scadden, David T., Duda, Dan G., Fukumura, Dai, Jain, Rakesh K.
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description <jats:p>Efficient generation of competent vasculogenic cells is a critical challenge of human induced pluripotent stem (hiPS) cell-based regenerative medicine. Biologically relevant systems to assess functionality of the engineered vessels in vivo are equally important for such development. Here, we report a unique approach for the derivation of endothelial precursor cells from hiPS cells using a triple combination of selection markers—CD34, neuropilin 1, and human kinase insert domain-containing receptor—and an efficient 2D culture system for hiPS cell-derived endothelial precursor cell expansion. With these methods, we successfully generated endothelial cells (ECs) from hiPS cells obtained from healthy donors and formed stable functional blood vessels in vivo, lasting for 280 d in mice. In addition, we developed an approach to generate mesenchymal precursor cells (MPCs) from hiPS cells in parallel. Moreover, we successfully generated functional blood vessels in vivo using these ECs and MPCs derived from the same hiPS cell line. These data provide proof of the principle that autologous hiPS cell-derived vascular precursors can be used for in vivo applications, once safety and immunological issues of hiPS-based cellular therapy have been resolved. Additionally, the durability of hiPS-derived blood vessels in vivo demonstrates a potential translation of this approach in long-term vascularization for tissue engineering and treatment of vascular diseases. Of note, we have also successfully generated ECs and MPCs from type 1 diabetic patient-derived hiPS cell lines and use them to generate blood vessels in vivo, which is an important milestone toward clinical translation of this approach.</jats:p>
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spelling Samuel, Rekha Daheron, Laurence Liao, Shan Vardam, Trupti Kamoun, Walid S. Batista, Ana Buecker, Christa Schäfer, Richard Han, Xiaoxing Au, Patrick Scadden, David T. Duda, Dan G. Fukumura, Dai Jain, Rakesh K. 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.1310675110 <jats:p>Efficient generation of competent vasculogenic cells is a critical challenge of human induced pluripotent stem (hiPS) cell-based regenerative medicine. Biologically relevant systems to assess functionality of the engineered vessels in vivo are equally important for such development. Here, we report a unique approach for the derivation of endothelial precursor cells from hiPS cells using a triple combination of selection markers—CD34, neuropilin 1, and human kinase insert domain-containing receptor—and an efficient 2D culture system for hiPS cell-derived endothelial precursor cell expansion. With these methods, we successfully generated endothelial cells (ECs) from hiPS cells obtained from healthy donors and formed stable functional blood vessels in vivo, lasting for 280 d in mice. In addition, we developed an approach to generate mesenchymal precursor cells (MPCs) from hiPS cells in parallel. Moreover, we successfully generated functional blood vessels in vivo using these ECs and MPCs derived from the same hiPS cell line. These data provide proof of the principle that autologous hiPS cell-derived vascular precursors can be used for in vivo applications, once safety and immunological issues of hiPS-based cellular therapy have been resolved. Additionally, the durability of hiPS-derived blood vessels in vivo demonstrates a potential translation of this approach in long-term vascularization for tissue engineering and treatment of vascular diseases. Of note, we have also successfully generated ECs and MPCs from type 1 diabetic patient-derived hiPS cell lines and use them to generate blood vessels in vivo, which is an important milestone toward clinical translation of this approach.</jats:p> Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells Proceedings of the National Academy of Sciences
spellingShingle Samuel, Rekha, Daheron, Laurence, Liao, Shan, Vardam, Trupti, Kamoun, Walid S., Batista, Ana, Buecker, Christa, Schäfer, Richard, Han, Xiaoxing, Au, Patrick, Scadden, David T., Duda, Dan G., Fukumura, Dai, Jain, Rakesh K., Proceedings of the National Academy of Sciences, Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells, Multidisciplinary
title Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_full Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_fullStr Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_full_unstemmed Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_short Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_sort generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
title_unstemmed Generation of functionally competent and durable engineered blood vessels from human induced pluripotent stem cells
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.1310675110