Level C· Early human research exploring benefitsProspective StudyPubMed

Construction of engineered 3D islet micro-tissue using porcine decellularized ECM for the treatment of diabetes.

Wang X., Jin L., Liu W., Stingelin L., Zhang P., Tan Z.

Prospective Study on Systemic / IV, published in Biomater Sci (2023) — summary generated from the PubMed abstract.

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Level C· Early human research exploring benefitsEvidence level of this study

Early human evidence such as case series or small samples is exploring possible benefits.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Prospective Study
Journal
Biomater Sci (2023)
Country
England
Reported sample size
—
Source database
PubMed
PMID
37387616
DOI
10.1039/d3bm00346a
Citations
8

Abstract (original English)

Islet transplantation improves diabetes patients' long-term blood glucose control, but its success and utility are limited by cadaver availability, quality, and considerable islet loss after transplantation due to ischemia and inadequate angiogenesis. This study used adipose, pancreatic, and liver tissue decellularized extracellular matrix (dECM) hydrogels in an effort to recapitulate the islet sites inside the pancreas in vitro , and successfully generated viable and functional heterocellular islet micro-tissues using islet cells, human umbilical vein endothelial cells, and adipose-derived mesenchymal stem cells. The three-dimensional (3D) islet micro-tissues maintained prolonged viability and normal secretory function, and showed high drug sensitivity in drug testing. Meanwhile, the 3D islet micro-tissues significantly enhanced survival and graft function in a mouse model of diabetes. These supportive 3D physiomimetic dECM hydrogels can be used not only for islet micro-tissue culture in vitro , but also have great promise for islet transplantation for the treatment of diabetes.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.

Evidence level

Early human evidence such as case series or small samples is exploring possible benefits.

How we grade evidence
MiceHumansAnimalsSwineDecellularized Extracellular MatrixExtracellular MatrixDiabetes MellitusHydrogelsHuman Umbilical Vein Endothelial Cells

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