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Decellularized Pancreatic Tail as Matrix for Pancreatic Islet Transplantation into the Greater Omentum in Rats

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    SYSNO ASEP0565357
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleDecellularized Pancreatic Tail as Matrix for Pancreatic Islet Transplantation into the Greater Omentum in Rats
    Author(s) Berková, Z. (CZ)
    Zacharovová, K. (CZ)
    Pátiková, A. (CZ)
    Leontovyc, I. (CZ)
    Hladíková, Z. (CZ)
    Červený, D. (CZ)
    Tihlaříková, Eva (UPT-D) RID, ORCID, SAI
    Neděla, Vilém (UPT-D) RID, ORCID, SAI
    Girman, P. (CZ)
    Jirák, D. (CZ)
    Saudek, F. (CZ)
    Article number171
    Source TitleJournal of Functional Biomaterials. - : MDPI - ISSN 2079-4983
    Roč. 13, č. 4 (2022)
    Number of pages17 s.
    Publication formOnline - E
    Languageeng - English
    CountryCH - Switzerland
    Keywordspancreas decellularization ; splenic vein perfusion ; extracellular matrix skeletons ; transplantation into the omentum ; advanced environmental scanning electron microscopy
    Subject RIVFB - Endocrinology, Diabetology, Metabolism, Nutrition
    OECD categoryEndocrinology and metabolism (including diabetes, hormones)
    R&D ProjectsGA22-25799S GA ČR - Czech Science Foundation (CSF)
    Method of publishingOpen access
    Institutional supportUPT-D - RVO:68081731
    UT WOS000901294600001
    EID SCOPUS85144872942
    DOI10.3390/jfb13040171
    AnnotationInfusing pancreatic islets into the portal vein currently represents the preferred approach for islet transplantation, despite considerable loss of islet mass almost immediately after implantation. Therefore, approaches that obviate direct intravascular placement are urgently needed. A promising candidate for extrahepatic placement is the omentum. We aimed to develop an extracellular matrix skeleton from the native pancreas that could provide a microenvironment for islet survival in an omental flap. To that end, we compared different decellularization approaches, including perfusion through the pancreatic duct, gastric artery, portal vein, and a novel method through the splenic vein. Decellularized skeletons were compared for size, residual DNA content, protein composition, histology, electron microscopy, and MR imaging after repopulation with isolated islets. Compared to the other approaches, pancreatic perfusion via the splenic vein provided smaller extracellular matrix skeletons, which facilitated transplantation into the omentum, without compromising other requirements, such as the complete depletion of cellular components and the preservation of pancreatic extracellular proteins. Repeated MR imaging of iron-oxide-labeled pancreatic islets showed that islets maintained their position in vivo for 49 days. Advanced environmental scanning electron microscopy demonstrated that islets remained integrated with the pancreatic skeleton. This novel approach represents a proof-of-concept for long-term transplantation experiments.
    WorkplaceInstitute of Scientific Instruments
    ContactMartina Šillerová, sillerova@ISIBrno.Cz, Tel.: 541 514 178
    Year of Publishing2023
    Electronic addresshttps://www.mdpi.com/2079-4983/13/4/171
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