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Temporal Dynamics of Metabolic Acquisition in Grafted Engineered Human Liver Tissue.
Fortin, Chelsea L; McCray, Tara N; Saxton, Sarah H; Johansson, Fredrik; Andino, Christian B; Mene, Jonathan; Wang, Yuliang; Stevens, Kelly R.
Afiliação
  • Fortin CL; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, Washington, 98109, USA.
  • McCray TN; Department of Bioengineering, University of Washington, Seattle, Washington, 98105, USA.
  • Saxton SH; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, 98195, USA.
  • Johansson F; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, Washington, 98109, USA.
  • Andino CB; Department of Bioengineering, University of Washington, Seattle, Washington, 98105, USA.
  • Mene J; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, Washington, 98109, USA.
  • Wang Y; Department of Bioengineering, University of Washington, Seattle, Washington, 98105, USA.
  • Stevens KR; Institute for Stem Cell & Regenerative Medicine, University of Washington, Seattle, Washington, 98109, USA.
Adv Biol (Weinh) ; 7(5): e2200208, 2023 05.
Article em En | MEDLINE | ID: mdl-36328790
Liver disease affects millions globally, and end-stage liver failure is only cured by organ transplant. Unfortunately, there is a growing shortage of donor organs as well as inequitable access to transplants across populations. Engineered liver tissue grafts that supplement or replace native organ function can address this challenge. While engineered liver tissues have been successfully engrafted previously, the extent to which these tissues express human liver metabolic genes and proteins remains unknown. Here, it is built engineered human liver tissues and characterized their engraftment, expansion, and metabolic phenotype at sequential stages post-implantation by RNA sequencing, histology, and host serology. Expression of metabolic genes is observed at weeks 1-2, followed by the cellular organization into hepatic cords by weeks 4-9.5. Furthermore, grafted engineered tissues exhibited progressive spatially restricted expression of critical functional proteins known to be zonated in the native human liver. This is the first report of engineered human liver tissue zonation after implantation in vivo, which can have important translational implications for this field.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Órgãos / Transplante de Fígado / Doença Hepática Terminal Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transplante de Órgãos / Transplante de Fígado / Doença Hepática Terminal Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article