Evidence map›Paper›PMID 38477407›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Genetically Encoded XTEN-based Hydrogels with Tunable Viscoelasticity and Biodegradability for Injectable Cell Therapies.

Jennifer I Bennett, Mary O'Kelly Boit, Nicole E Gregorio, Fan Zhang, Ryan D Kibler, Jack W Hoye, Olivia Prado, Peter B Rapp, Charles E Murry, Kelly R Stevens and 1 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

22 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Enzyme-Integrated Hydrogels for Advanced Biological Applications.Polymer science & technology (Washington, D.C.) · 2026
    Review
  7. Article
  8. Article
  9. Stimuli-triggered formation ofCell biomaterials · 2026
    Article
  10. Article
  11. Review
  12. Enzymatic Methods for Assembling and Modifying Hydrogel Biomaterials.Regenerative engineering and translational medicine · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article
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

11 authors at 3 institutions in 3 countries.

Jennifer I BennettDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0003-2565-1267
Mary O'Kelly BoitDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0001-9990-6950
Nicole E GregorioDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0002-7287-209X
Fan ZhangDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0001-6754-7500
Ryan D KiblerDepartment of Biochemistry, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0001-6984-9887
Jack W HoyeDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0009-0003-8251-731X
Olivia PradoDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0003-4926-363X
Peter B RappFlagship Labs 83, Inc., 135 Morrissey Blvd., Boston, MA, 02125, USA.ORCID 0000-0002-9586-2126
Charles E MurryDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0003-3862-6773
Kelly R StevensDepartment of Bioengineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0002-4024-2990
Cole A DeForestDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98105, USA.ORCID 0000-0003-0337-3577
University of Washington · USCalifornia Institute for Regenerative Medicine · USUniversity of Massachusetts Boston · US

Funding

Bioengineering Cardiovascular Training GrantT32EB001650 · NIBIB · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2004 to 2019
$3.6M
Mechanisms of Cell-Based Heart RegenerationR01HL146868 · NHLBI · UNIVERSITY OF WASHINGTON · PI MURRY, CHARLES E, SNIADECKI, NATHAN JOHN · 2019 to 2022
$3.5M
Photoabsorbing bioinks for expanding 3D printed human liver in situR01DK128551 · NIDDK · UNIVERSITY OF WASHINGTON · PI STEVENS, KELLY R · 2021 to 2024
$3.0M
Metabolic and Transcriptional Reprogramming of Cardiac MaturationR01HL148081 · NHLBI · UNIVERSITY OF WASHINGTON · PI MURRY, CHARLES E · 2021 to 2024
$2.5M
Mimicking, Exploiting, and Understanding Biology's Heterogeneity in 4DR35GM138036 · NIGMS · UNIVERSITY OF WASHINGTON · PI Cole A DeForest · 2020 to 2026
$2.3M
Zwitterionic Injectable Pellet (ZIP) microgels as an injectable cell carrier for iPSC-CMs for myocardial repairF31HL152626 · NHLBI · UNIVERSITY OF WASHINGTON · PI BOIT, MARY O'KELLY · 2020 to 2021
$85k
National Science Foundation DGE-2140004National Science Foundation DMR 1652141NHLBI NIH HHS 1F31HL152626NHLBI NIH HHS F31 HL152626NHLBI NIH HHS R01 HL146868NHLBI NIH HHS R01 HL148081NIBIB NIH HHS T32 EB001650NIBIB NIH HHS T32EB001650NIDDK NIH HHS R01 DK128551NIDDK NIH HHS R01DK128551NIDDK NIH HHS R01HL146868NIDDK NIH HHS R01HL148081NIGMS NIH HHS R35 GM138036NIGMS NIH HHS R35GM138036NIH HHS 1F31HL152626-01NIH HHS T32EB001650Paul G. Allen Family Foundation
6 · The paper itself

Abstract

While direct cell transplantation holds great promise in treating many debilitating diseases, poor cell survival and engraftment following injection have limited effective clinical translation. Though injectable biomaterials offer protection against membrane-damaging extensional flow and supply a supportive 3D environment in vivo that ultimately improves cell retention and therapeutic costs, most are created from synthetic or naturally harvested polymers that are immunogenic and/or chemically ill-defined. This work presents a shear-thinning and self-healing telechelic recombinant protein-based hydrogel designed around XTEN - a well-expressible, non-immunogenic, and intrinsically disordered polypeptide previously evolved as a genetically encoded alternative to PEGylation to "eXTENd" the in vivo half-life of fused protein therapeutics. By flanking XTEN with self-associating coil domains derived from cartilage oligomeric matrix protein, single-component physically crosslinked hydrogels exhibiting rapid shear thinning and self-healing through homopentameric coiled-coil bundling are formed. Individual and combined point mutations that variably stabilize coil association enables a straightforward method to genetically program material viscoelasticity and biodegradability. Finally, these materials protect and sustain viability of encapsulated human fibroblasts, hepatocytes, embryonic kidney (HEK), and embryonic stem-cell-derived cardiomyocytes (hESC-CMs) through culture, injection, and transcutaneous implantation in mice. These injectable XTEN-based hydrogels show promise for both in vitro cell culture and in vivo cell transplantation applications.

Indexed as

Biocompatible MaterialsHydrogelsAnimalsCell- and Tissue-Based TherapyElasticityElastinHumansMiceViscosityBiocompatible MaterialsElastinHydrogelsbiomaterialbiopolymercoiled‐coilhydrogelsinjectableproteinXTEN

Identifiers

PMID38477407
PMCPMC11200090
OpenAlexW4392761646

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.