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De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models
Ex vivo lung perfusion (EVLP) has increased donor lung utilization through assessment of “marginal” lungs prior to transplantation. To develop it as a donor lung reconditioning platform, prolonged EVLP is necessary, and new perfusates are required to provide sufficient nutritional support. Human pul...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487937/ https://www.ncbi.nlm.nih.gov/pubmed/37685927 http://dx.doi.org/10.3390/ijms241713117 |
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author | Huang, Lei Vellanki, Ravi N. Zhu, Zhiyuan Wouters, Bradly G. Keshavjee, Shaf Liu, Mingyao |
author_facet | Huang, Lei Vellanki, Ravi N. Zhu, Zhiyuan Wouters, Bradly G. Keshavjee, Shaf Liu, Mingyao |
author_sort | Huang, Lei |
collection | PubMed |
description | Ex vivo lung perfusion (EVLP) has increased donor lung utilization through assessment of “marginal” lungs prior to transplantation. To develop it as a donor lung reconditioning platform, prolonged EVLP is necessary, and new perfusates are required to provide sufficient nutritional support. Human pulmonary microvascular endothelial cells and epithelial cells were used to test different formulas for basic cellular function. A selected formula was further tested on an EVLP cell culture model, and cell confluence, apoptosis, and GSH and HSP70 levels were measured. When a cell culture medium (DMEM) was mixed with a current EVLP perfusate—Steen solution, DMEM enhanced cell confluence and migration and reduced apoptosis in a dose-dependent manner. A new EVLP perfusate was designed and tested based on DMEM. The final formula contains 5 g/L Dextran-40 and 7% albumin and is named as D05D7A solution. It inhibited cold static storage and warm reperfusion-induced cell apoptosis, improved cell confluence, and enhanced GSH and HSP70 levels in human lung cells compared to Steen solution. DMEM-based nutrient-rich EVLP perfusate could be a promising formula to prolong EVLP and support donor lung repair, reconditioning and further improve donor lung quality and quantity for transplantation with better clinical outcome. |
format | Online Article Text |
id | pubmed-10487937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104879372023-09-09 De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models Huang, Lei Vellanki, Ravi N. Zhu, Zhiyuan Wouters, Bradly G. Keshavjee, Shaf Liu, Mingyao Int J Mol Sci Article Ex vivo lung perfusion (EVLP) has increased donor lung utilization through assessment of “marginal” lungs prior to transplantation. To develop it as a donor lung reconditioning platform, prolonged EVLP is necessary, and new perfusates are required to provide sufficient nutritional support. Human pulmonary microvascular endothelial cells and epithelial cells were used to test different formulas for basic cellular function. A selected formula was further tested on an EVLP cell culture model, and cell confluence, apoptosis, and GSH and HSP70 levels were measured. When a cell culture medium (DMEM) was mixed with a current EVLP perfusate—Steen solution, DMEM enhanced cell confluence and migration and reduced apoptosis in a dose-dependent manner. A new EVLP perfusate was designed and tested based on DMEM. The final formula contains 5 g/L Dextran-40 and 7% albumin and is named as D05D7A solution. It inhibited cold static storage and warm reperfusion-induced cell apoptosis, improved cell confluence, and enhanced GSH and HSP70 levels in human lung cells compared to Steen solution. DMEM-based nutrient-rich EVLP perfusate could be a promising formula to prolong EVLP and support donor lung repair, reconditioning and further improve donor lung quality and quantity for transplantation with better clinical outcome. MDPI 2023-08-23 /pmc/articles/PMC10487937/ /pubmed/37685927 http://dx.doi.org/10.3390/ijms241713117 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Huang, Lei Vellanki, Ravi N. Zhu, Zhiyuan Wouters, Bradly G. Keshavjee, Shaf Liu, Mingyao De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title | De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title_full | De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title_fullStr | De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title_full_unstemmed | De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title_short | De Novo Design and Development of a Nutrient-Rich Perfusate for Ex Vivo Lung Perfusion with Cell Culture Models |
title_sort | de novo design and development of a nutrient-rich perfusate for ex vivo lung perfusion with cell culture models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10487937/ https://www.ncbi.nlm.nih.gov/pubmed/37685927 http://dx.doi.org/10.3390/ijms241713117 |
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