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In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure
Safe clinical hormone replacement (HR) will likely become increasingly important in the growing populations of aged women and cancer patients undergoing treatments that ablate the ovaries. Cell-based HRT (cHRT) is an alternative approach that may allow certain physiological outcomes to be achieved w...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717171/ https://www.ncbi.nlm.nih.gov/pubmed/29208899 http://dx.doi.org/10.1038/s41467-017-01851-3 |
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author | Sittadjody, Sivanandane Saul, Justin M. McQuilling, John P. Joo, Sunyoung Register, Thomas C. Yoo, James J. Atala, Anthony Opara, Emmanuel C. |
author_facet | Sittadjody, Sivanandane Saul, Justin M. McQuilling, John P. Joo, Sunyoung Register, Thomas C. Yoo, James J. Atala, Anthony Opara, Emmanuel C. |
author_sort | Sittadjody, Sivanandane |
collection | PubMed |
description | Safe clinical hormone replacement (HR) will likely become increasingly important in the growing populations of aged women and cancer patients undergoing treatments that ablate the ovaries. Cell-based HRT (cHRT) is an alternative approach that may allow certain physiological outcomes to be achieved with lower circulating hormone levels than pharmacological means due to participation of cells in the hypothalamus-pituitary-ovary feedback control loop. Here we describe the in vivo performance of 3D bioengineered ovarian constructs that recapitulate native cell–cell interactions between ovarian granulosa and theca cells as an approach to cHRT. The constructs are fabricated using either Ca(++) or Sr(++) to crosslink alginate. Following implantation in ovariectomized (ovx) rats, the Sr(++)-cross-linked constructs achieve stable secretion of hormones during 90 days of study. Further, we show these constructs with isogeneic cells to be effective in ameliorating adverse effects of hormone deficiency, including bone health, uterine health, and body composition in this rat model. |
format | Online Article Text |
id | pubmed-5717171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57171712017-12-08 In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure Sittadjody, Sivanandane Saul, Justin M. McQuilling, John P. Joo, Sunyoung Register, Thomas C. Yoo, James J. Atala, Anthony Opara, Emmanuel C. Nat Commun Article Safe clinical hormone replacement (HR) will likely become increasingly important in the growing populations of aged women and cancer patients undergoing treatments that ablate the ovaries. Cell-based HRT (cHRT) is an alternative approach that may allow certain physiological outcomes to be achieved with lower circulating hormone levels than pharmacological means due to participation of cells in the hypothalamus-pituitary-ovary feedback control loop. Here we describe the in vivo performance of 3D bioengineered ovarian constructs that recapitulate native cell–cell interactions between ovarian granulosa and theca cells as an approach to cHRT. The constructs are fabricated using either Ca(++) or Sr(++) to crosslink alginate. Following implantation in ovariectomized (ovx) rats, the Sr(++)-cross-linked constructs achieve stable secretion of hormones during 90 days of study. Further, we show these constructs with isogeneic cells to be effective in ameliorating adverse effects of hormone deficiency, including bone health, uterine health, and body composition in this rat model. Nature Publishing Group UK 2017-12-05 /pmc/articles/PMC5717171/ /pubmed/29208899 http://dx.doi.org/10.1038/s41467-017-01851-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sittadjody, Sivanandane Saul, Justin M. McQuilling, John P. Joo, Sunyoung Register, Thomas C. Yoo, James J. Atala, Anthony Opara, Emmanuel C. In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title | In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title_full | In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title_fullStr | In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title_full_unstemmed | In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title_short | In vivo transplantation of 3D encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
title_sort | in vivo transplantation of 3d encapsulated ovarian constructs in rats corrects abnormalities of ovarian failure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5717171/ https://www.ncbi.nlm.nih.gov/pubmed/29208899 http://dx.doi.org/10.1038/s41467-017-01851-3 |
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