Decellularized pancreatic tail as matrix for pancreatic islet transplantation into the greater omentum in rats
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F22%3A00083495" target="_blank" >RIV/00023001:_____/22:00083495 - isvavai.cz</a>
Alternative codes found
RIV/68081731:_____/22:00565357 RIV/46747885:24530/22:00010469 RIV/00216208:11110/22:10452458
Result on the web
<a href="https://www.mdpi.com/2079-4983/13/4/171" target="_blank" >https://www.mdpi.com/2079-4983/13/4/171</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/jfb13040171" target="_blank" >10.3390/jfb13040171</a>
Alternative languages
Result language
angličtina
Original language name
Decellularized pancreatic tail as matrix for pancreatic islet transplantation into the greater omentum in rats
Original language description
Infusing 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.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
20601 - Medical engineering
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2022
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of functional biomaterials
ISSN
2079-4983
e-ISSN
2079-4983
Volume of the periodical
13
Issue of the periodical within the volume
4
Country of publishing house
CH - SWITZERLAND
Number of pages
17
Pages from-to
"art. no. 171"
UT code for WoS article
000901294600001
EID of the result in the Scopus database
2-s2.0-85144872942