Evidence map›Paper›PMID 18773957›Full record

ArticleMatrix biology : journal of the International Society for Matrix Biology2008

Hydrogel encapsulation environments functionalized with extracellular matrix interactions increase islet insulin secretion.

Laney M Weber, Kristi S Anseth

Abstract read
In one paragraph

Article in Matrix biology : journal of the International Society for Matrix Biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
6.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 152 citations in OpenAlex.

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  18. Article
  19. An Overview of Engineered Hydrogel-Based Biomaterials for ImprovedFrontiers in bioengineering and biotechnology · 2021
    Review
  20. Article

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Laney M WeberDepartment of Chemical and Biological Engineering, Howard Hughes Medical Institute, University of Colorado, Boulder, CO 80309-0424, USA.
Kristi S Anseth
University of Colorado Boulder · US

Funding

Bioactive Gels that Promote Long-Term Islet Survival and FunctionR01DK076084 · NIDDK · UNIVERSITY OF COLORADO · PI ANSETH, KRISTI S. · 2008 to 2012
$1.9M
Howard Hughes Medical InstituteNIDDK NIH HHS 1R01 DK076084-01A2NIDDK NIH HHS R01 DK076084
6 · The paper itself

Abstract

The individual and synergistic effects of extracellular matrix interactions on isolated islet function in culture were investigated within a three-dimensional poly(ethylene glycol) (PEG) hydrogel encapsulation environment. First, we observed similar glucose-stimulated insulin secretion from unencapsulated murine islets and islets photoencapsulated in PEG gels. Then islets were encapsulated in gels containing the basement membrane proteins collagen type IV and laminin, individually and in combination, at a total protein concentration of 100 microg/ml, and islet insulin secretion in response to high glucose was measured over time. Specific laminin interactions were investigated via islet encapsulation with adhesive peptide sequences found in laminin as well as via functional blocking of cell surface receptors known to bind laminin. Over 32 days, islet interactions with collagen type IV and laminin localized within the three-dimensional extracellular environment contributed to two-fold and four-fold increases in insulin secretion, respectively, relative to islets encapsulated without matrix proteins. Hydrogel compositions containing both matrix proteins and >75% laminin further increased islet insulin secretion to approximately six-fold that of islets encapsulated in the absence of matrix proteins. Encapsulation with the peptide sequence IKVAV resulted in increased islet insulin secretion, but not to the extent observed in the presence of whole laminin. Increased insulin secretion in the presence of laminin was eliminated when islets were exposed to functionally blocking anti-alpha6 integrin antibody prior to islet encapsulation with laminin. Our results demonstrate the potential of specific matrix interactions within an islet encapsulation microenvironment to promote encapsulated islet function.

Indexed as

Hydrogel, Polyethylene Glycol DimethacrylateAnimalsCapsulesExtracellular MatrixGlucoseInsulinInsulin SecretionIslets of LangerhansLamininMiceMice, Inbred BALB CPolyethylene GlycolsReceptors, Cell SurfaceCapsulesextracellular matrix receptorGlucoseHydrogel, Polyethylene Glycol DimethacrylateInsulinLamininPolyethylene GlycolsReceptors, Cell Surface

Identifiers

PMID18773957
PMCPMC2631362
OpenAlexW2035259469

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.