ACELLULAR TRACHEAL CARTILAGINOUS SCAFFOLD PRODUCING FOR TISSUE-ENGINEERED CONSTRUCTS
- Authors: Baranovsky D.S.1, Demchenko A.G.1, Oganesyan R.V.1, Lebedev G.V.2, Berseneva D.A.1, Balyasin M.V.1, Parshin V.D.1, Lyundup A.V.1
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Affiliations:
- Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
- Lomonosov Moscow State University
- Issue: Vol 72, No 4 (2017)
- Pages: 254-260
- Section: CELL TRANSPLANTOLOGY AND TISSUE ENGINEERING: CURRENT ISSUES
- Published: 16.06.2017
- URL: https://vestnikramn.spr-journal.ru/jour/article/view/723
- DOI: https://doi.org/10.15690/vramn723
- ID: 723
Cite item
Full Text
Abstract
Background: Tissue-engineered trachea transplantation remains the last chance for a variety of patients suffering from severe cicatricial tracheal stenosis. Despite the series of carried studies, the final solution hasn’t been found. Creating a functionally complete hyaline cartilage graft in vitro still presents a fundamental problem, and a number of researchers consider it as the key to a successful tracheal tissue-engineering.
Aims: The study aimed to investigate the capability of detergent complex and DNAse I for human tracheal cartilage decellularization in short-time exposition for acellular scaffold obtaining.
Materials and methods: Isolated from cadaveric trachea human native cartilage was used for decellularization by ensimatic-detergent complex including Triton X-100, DMSO, and DNAse I. The scaffold was characterised by histological examinations, analysis of the residual DNA content, and cell metabolic activity colorimetric test with culture in the scaffold fragments.
Results: The obtained scaffolds presented highly porous structure mostly composed of collagen and glycosaminoglycans with an insignificant residual DNA level, absence of citotoxicity, and capability for cell proliferative activity stimulation.
Conclusions: Thus, the study provides a new short-time technology for hyaline cartilage decellularization in order to achieve acellular scaffolds in step with the tissue engineering requirements.
About the authors
D. S. Baranovsky
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Author for correspondence.
Email: doc.baranovsky@gmail.com
ORCID iD: 0000-0002-6154-9959
Научный сотрудник Института регенеративной медицины.
119991, Москва, ул. Трубецкая, д. 8, стр. 2.
SPIN-код: 6913-6361
РоссияA. G. Demchenko
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: demchenkoann@yandex.ru
ORCID iD: 0000-0002-4460-7627
Студент-лаборант 3-го курса Института регенеративной медицины.
119991, Москва, ул. Трубецкая, д. 8, стр. 2.
SPIN-код: 3779-9060
РоссияR. V. Oganesyan
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: oganesyan.rv@gmail.com
ORCID iD: 0000-0001-8967-5597
Студент 5-го курса Института регенеративной медицины.
119991, Москва, ул. Трубецкая, д. 8, стр. 2.
SPIN-код: 8106-3394
РоссияG. V. Lebedev
Lomonosov Moscow State University
Email: lebedev.george12@gmail.com
ORCID iD: 0000-0001-8493-3390
Студент 2-го курса.
119991, Москва, Ломоносовский проспект, д. 1.
SPIN-код: 2050-4004
РоссияD. A. Berseneva
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: berseneva1410@rambler.ru
ORCID iD: 0000-0001-5970-2240
Moscow Россия
M. V. Balyasin
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: max160203@gmail.com
ORCID iD: 0000-0002-3097-344X
Moscow Россия
V. D. Parshin
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: vdparshin@yandex.ru
Moscow Россия
A. V. Lyundup
Sechenov First Moscow State Medical University Ministry of Health of Russian Federation
Email: lyundup@gmail.com
ORCID iD: 0000-0002-0102-5491
Кандидат медицинских наук, заведующий отделением клеточных технологий Института регенеративной медицины.
119991, Москва, ул. Трубецкая, д. 8, стр. 2, тел.: +7 (495) 609-14-00.
SPIN-код: 4954-3004
РоссияReferences
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