Modification of decellularized vascular xenografts with 8-arm polyethylene glycol suppresses macrophage infiltration but maintains graft degradability.


Journal

Journal of biomedical materials research. Part A
ISSN: 1552-4965
Titre abrégé: J Biomed Mater Res A
Pays: United States
ID NLM: 101234237

Informations de publication

Date de publication:
10 2020
Historique:
received: 12 12 2019
revised: 19 03 2020
accepted: 28 03 2020
pubmed: 24 4 2020
medline: 4 11 2021
entrez: 24 4 2020
Statut: ppublish

Résumé

Because acellular vascular xenografts induce an immunological reaction through macrophage infiltration, they are conventionally crosslinked with glutaraldehyde (GA). However, the GA crosslinking reaction inhibits not only the host immune reaction around the graft but also the graft's enzymatic degradability, which is one of the key characteristics of acellular grafts that allow them to be replaced by host tissue. In this study, we used an 8-arm polyethylene glycol (PEG) to successfully suppress macrophage infiltration, without eliminating graft degradation. Decellularized ostrich carotid arteries were modified with GA or N-hydroxysuccinimide-activated 8-arm PEG (8-arm PEG-NHS), which has a molecular weight of 17 kDa. To evaluate the enzymatic degradation in vitro, the graft was immersed in a collagenase solution for 12 hr. The 8-arm PEG-modified graft was degraded to the same extent as the unmodified graft, but the GA-modified graft was not degraded. The graft was transplanted into rat subcutaneous tissue for up to 8 weeks. Although CD68-positive cells accumulated in the unmodified graft, they did not infiltrate into either modified graft. However, the GA-modified grafts calcified, but the 8-arm PEG-modified graft did not calcify after transplantation. These data suggested that 8-arm PEG-NHS is a promising modification agent for biodegradable vascular xenografts, to suppress acute macrophage infiltration only.

Identifiants

pubmed: 32323458
doi: 10.1002/jbm.a.36960
doi:

Substances chimiques

Cross-Linking Reagents 0
Polyethylene Glycols 3WJQ0SDW1A
Glutaral T3C89M417N

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2005-2014

Informations de copyright

© 2020 Wiley Periodicals, Inc.

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Auteurs

Atsushi Mahara (A)

Department of Biomedical Engineering, National Cerebral and Cardiovascular Center Research Institute, Kishibe Shin-machi Suita Osaka, Japan.

Marina Kitai (M)

Department of Biomedical Engineering, National Cerebral and Cardiovascular Center Research Institute, Kishibe Shin-machi Suita Osaka, Japan.
Faculty of Chemistry, Materials and Bioengineering, Kansai University, 3-3-35 Yamatecho, Suita, Osaka, Japan.

Hiroyasu Masunaga (H)

Registered Institution for Facilities Use Promotion, Japan Synchrotoron Radiation Research Institute (JASRI), Sayo-gun, Hyogo, Japan.

Takaaki Hikima (T)

Registered Institution for Facilities Use Promotion, Japan Synchrotoron Radiation Research Institute (JASRI), Sayo-gun, Hyogo, Japan.

Yuichi Ohya (Y)

Faculty of Chemistry, Materials and Bioengineering, Kansai University, 3-3-35 Yamatecho, Suita, Osaka, Japan.

Sono Sasaki (S)

Department of Biobased Materials Science, Kyoto Institute of Technology, Kyoto, Japan.

Shinichi Sakurai (S)

Department of Biobased Materials Science, Kyoto Institute of Technology, Kyoto, Japan.

Tetsuji Yamaoka (T)

Department of Biomedical Engineering, National Cerebral and Cardiovascular Center Research Institute, Kishibe Shin-machi Suita Osaka, Japan.

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