A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink

Upon bioprinting, cells are mixed with a biomaterial to fabricate a living tissue, thus emphasizing the importance of biomaterials. The biomaterial used in this study was a bio-ink prepared using skin decellularized extracellular matrix (dECM). Skin dECM was extracted by treating the dermis with che...

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Main Authors: Joo-Yun Won, Mi-Hee Lee, Mi-Jeong Kim, Kyung-Hyun Min, Geunseon Ahn, Ji-Seok Han, Songwan Jin, Won-Soo Yun, Jin-Hyung Shim
Format: Article
Language:English
Published: Taylor & Francis Group 2019-12-01
Series:Artificial Cells, Nanomedicine, and Biotechnology
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Online Access:https://www.tandfonline.com/doi/10.1080/21691401.2019.1575842
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author Joo-Yun Won
Mi-Hee Lee
Mi-Jeong Kim
Kyung-Hyun Min
Geunseon Ahn
Ji-Seok Han
Songwan Jin
Won-Soo Yun
Jin-Hyung Shim
author_facet Joo-Yun Won
Mi-Hee Lee
Mi-Jeong Kim
Kyung-Hyun Min
Geunseon Ahn
Ji-Seok Han
Songwan Jin
Won-Soo Yun
Jin-Hyung Shim
author_sort Joo-Yun Won
collection DOAJ
description Upon bioprinting, cells are mixed with a biomaterial to fabricate a living tissue, thus emphasizing the importance of biomaterials. The biomaterial used in this study was a bio-ink prepared using skin decellularized extracellular matrix (dECM). Skin dECM was extracted by treating the dermis with chemicals and enzymes; the basic structural and functional proteins of the ECM, including collagen, glycosaminoglycans (GAGs), bioreactive materials and growth factors, were preserved, whereas the resident cells that might cause immune rejection or inflammatory responses were removed. The bio-ink based on dECM powder, together with human dermal fibroblasts (HDFs), was loaded into the nozzle of the 3D bioprinter to create the 3D construct. This construct underwent gelation with changing temperature while its shape was maintained for 7 days. The cells showed over 90% viability and proliferation. By analysing the gene expression pattern in the cells of the construct, the skin regenerative mechanism of the bio-ink was verified. Microarray results confirmed that the gene expression related to skin morphology and development had been enhanced because the bioreactive molecules and growth factors, in addition to residual ECM in dECM, provided an optimal condition for the HDFs.
format Article
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institution Kabale University
issn 2169-1401
2169-141X
language English
publishDate 2019-12-01
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series Artificial Cells, Nanomedicine, and Biotechnology
spelling doaj-art-6f45179ddcc04261a4c037ea0b0bd2fb2025-08-20T03:51:24ZengTaylor & Francis GroupArtificial Cells, Nanomedicine, and Biotechnology2169-14012169-141X2019-12-0147164464910.1080/21691401.2019.1575842A potential dermal substitute using decellularized dermis extracellular matrix derived bio-inkJoo-Yun Won0Mi-Hee Lee1Mi-Jeong Kim2Kyung-Hyun Min3Geunseon Ahn4Ji-Seok Han5Songwan Jin6Won-Soo Yun7Jin-Hyung Shim8Research Institute, T&R Biofab Co. Ltd., Siheung-si, Republic of KoreaResearch Institute, T&R Biofab Co. Ltd., Siheung-si, Republic of KoreaResearch Institute, T&R Biofab Co. Ltd., Siheung-si, Republic of KoreaResearch Institute, T&R Biofab Co. Ltd., Siheung-si, Republic of KoreaResearch Institute, T&R Biofab Co. Ltd., Siheung-si, Republic of KoreaDepartment of Advanced Toxicology Research, Korea Institute of Toxicology (KIT), Daejeon, Republic of KoreaDepartment of Mechanical Engineering, Korea Polytechnic University, Siheung-si, Republic of KoreaDepartment of Mechanical Engineering, Korea Polytechnic University, Siheung-si, Republic of KoreaDepartment of Mechanical Engineering, Korea Polytechnic University, Siheung-si, Republic of KoreaUpon bioprinting, cells are mixed with a biomaterial to fabricate a living tissue, thus emphasizing the importance of biomaterials. The biomaterial used in this study was a bio-ink prepared using skin decellularized extracellular matrix (dECM). Skin dECM was extracted by treating the dermis with chemicals and enzymes; the basic structural and functional proteins of the ECM, including collagen, glycosaminoglycans (GAGs), bioreactive materials and growth factors, were preserved, whereas the resident cells that might cause immune rejection or inflammatory responses were removed. The bio-ink based on dECM powder, together with human dermal fibroblasts (HDFs), was loaded into the nozzle of the 3D bioprinter to create the 3D construct. This construct underwent gelation with changing temperature while its shape was maintained for 7 days. The cells showed over 90% viability and proliferation. By analysing the gene expression pattern in the cells of the construct, the skin regenerative mechanism of the bio-ink was verified. Microarray results confirmed that the gene expression related to skin morphology and development had been enhanced because the bioreactive molecules and growth factors, in addition to residual ECM in dECM, provided an optimal condition for the HDFs.https://www.tandfonline.com/doi/10.1080/21691401.2019.1575842dECMbio-ink3D bioprintingmicroarraytissue regeneration
spellingShingle Joo-Yun Won
Mi-Hee Lee
Mi-Jeong Kim
Kyung-Hyun Min
Geunseon Ahn
Ji-Seok Han
Songwan Jin
Won-Soo Yun
Jin-Hyung Shim
A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
Artificial Cells, Nanomedicine, and Biotechnology
dECM
bio-ink
3D bioprinting
microarray
tissue regeneration
title A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
title_full A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
title_fullStr A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
title_full_unstemmed A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
title_short A potential dermal substitute using decellularized dermis extracellular matrix derived bio-ink
title_sort potential dermal substitute using decellularized dermis extracellular matrix derived bio ink
topic dECM
bio-ink
3D bioprinting
microarray
tissue regeneration
url https://www.tandfonline.com/doi/10.1080/21691401.2019.1575842
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