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Cardiac-mimetic cell-culture system for direct cardiac reprogramming
Rationale: Cardiovascular diseases often cause substantial heart damage and even heart failure due to the limited regenerative capacity of adult cardiomyocytes. The direct cardiac reprogramming of fibroblasts could be a promising therapeutic option for these patients. Although exogenous transcriptio...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815967/ https://www.ncbi.nlm.nih.gov/pubmed/31660065 http://dx.doi.org/10.7150/thno.35574 |
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author | Song, Seuk Young Yoo, Jin Go, Seokhyeong Hong, Jihye Sohn, Hee Su Lee, Ju-Ro Kang, Mikyung Jeong, Gun-Jae Ryu, Seungmi Kim, Seung Hyun L. Hwang, Nathaniel S. Char, Kookheon Kim, Byung-Soo |
author_facet | Song, Seuk Young Yoo, Jin Go, Seokhyeong Hong, Jihye Sohn, Hee Su Lee, Ju-Ro Kang, Mikyung Jeong, Gun-Jae Ryu, Seungmi Kim, Seung Hyun L. Hwang, Nathaniel S. Char, Kookheon Kim, Byung-Soo |
author_sort | Song, Seuk Young |
collection | PubMed |
description | Rationale: Cardiovascular diseases often cause substantial heart damage and even heart failure due to the limited regenerative capacity of adult cardiomyocytes. The direct cardiac reprogramming of fibroblasts could be a promising therapeutic option for these patients. Although exogenous transcriptional factors can induce direct cardiac reprogramming, the reprogramming efficiency is too low to be used clinically. Herein, we introduce a cardiac-mimetic cell-culture system that resembles the microenvironment in the heart and provides interactions with cardiomyocytes and electrical cues to the cultured fibroblasts for direct cardiac reprogramming. Methods: Nano-thin and nano-porous membranes and heart like electric stimulus were used in the cardiac-mimetic cell-culture system. The human neonatal dermal fibroblasts containing cardiac transcription factors were plated on the membrane and cultured with the murine cardiomyocyte in the presence of the electric stimulus. The reprogramming efficiency was evaluated by qRT-PCR and immunocytochemistry. Results: Nano-thin and nano-porous membranes in the culture system facilitated interactions between fibroblasts and cardiomyocytes in coculture. The cellular interactions and electric stimulation supplied by the culture system dramatically enhanced the cardiac reprogramming efficiency of cardiac-specific transcriptional factor-transfected fibroblasts. Conclusion: The cardiac-mimetic culture system may serve as an effective tool for producing a feasible number of reprogrammed cardiomyocytes from fibroblasts. |
format | Online Article Text |
id | pubmed-6815967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-68159672019-10-28 Cardiac-mimetic cell-culture system for direct cardiac reprogramming Song, Seuk Young Yoo, Jin Go, Seokhyeong Hong, Jihye Sohn, Hee Su Lee, Ju-Ro Kang, Mikyung Jeong, Gun-Jae Ryu, Seungmi Kim, Seung Hyun L. Hwang, Nathaniel S. Char, Kookheon Kim, Byung-Soo Theranostics Research Paper Rationale: Cardiovascular diseases often cause substantial heart damage and even heart failure due to the limited regenerative capacity of adult cardiomyocytes. The direct cardiac reprogramming of fibroblasts could be a promising therapeutic option for these patients. Although exogenous transcriptional factors can induce direct cardiac reprogramming, the reprogramming efficiency is too low to be used clinically. Herein, we introduce a cardiac-mimetic cell-culture system that resembles the microenvironment in the heart and provides interactions with cardiomyocytes and electrical cues to the cultured fibroblasts for direct cardiac reprogramming. Methods: Nano-thin and nano-porous membranes and heart like electric stimulus were used in the cardiac-mimetic cell-culture system. The human neonatal dermal fibroblasts containing cardiac transcription factors were plated on the membrane and cultured with the murine cardiomyocyte in the presence of the electric stimulus. The reprogramming efficiency was evaluated by qRT-PCR and immunocytochemistry. Results: Nano-thin and nano-porous membranes in the culture system facilitated interactions between fibroblasts and cardiomyocytes in coculture. The cellular interactions and electric stimulation supplied by the culture system dramatically enhanced the cardiac reprogramming efficiency of cardiac-specific transcriptional factor-transfected fibroblasts. Conclusion: The cardiac-mimetic culture system may serve as an effective tool for producing a feasible number of reprogrammed cardiomyocytes from fibroblasts. Ivyspring International Publisher 2019-09-19 /pmc/articles/PMC6815967/ /pubmed/31660065 http://dx.doi.org/10.7150/thno.35574 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Song, Seuk Young Yoo, Jin Go, Seokhyeong Hong, Jihye Sohn, Hee Su Lee, Ju-Ro Kang, Mikyung Jeong, Gun-Jae Ryu, Seungmi Kim, Seung Hyun L. Hwang, Nathaniel S. Char, Kookheon Kim, Byung-Soo Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title | Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title_full | Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title_fullStr | Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title_full_unstemmed | Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title_short | Cardiac-mimetic cell-culture system for direct cardiac reprogramming |
title_sort | cardiac-mimetic cell-culture system for direct cardiac reprogramming |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815967/ https://www.ncbi.nlm.nih.gov/pubmed/31660065 http://dx.doi.org/10.7150/thno.35574 |
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