Evidence map›Paper›PMID 38096646›Full record

ArticleBiomaterials advances2024

Using dynamic biomaterials to study the temporal role of bioactive peptides during osteogenesis.

Fallon M Fumasi, Tara MacCulloch, Julio Bernal-Chanchavac, Nicholas Stephanopoulos, Julianne L Holloway

Open access · greenAbstract read
In one paragraph

Article in Biomaterials advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Fallon M FumasiChemical Engineering, School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, AZ, United States of America.
Tara MacCullochBiodesign Center for Molecular Design and Biomimetics, Arizona State University, Tempe, AZ, United States of America; School of Molecular Sciences, Arizona State University, Tempe, AZ, United States of America.
Julio Bernal-ChanchavacBiodesign Center for Molecular Design and Biomimetics, Arizona State University, Tempe, AZ, United States of America; School of Molecular Sciences, Arizona State University, Tempe, AZ, United States of America. Electronic address: jcbernal@asu.edu.
Nicholas StephanopoulosBiodesign Center for Molecular Design and Biomimetics, Arizona State University, Tempe, AZ, United States of America; School of Molecular Sciences, Arizona State University, Tempe, AZ, United States of America. Electronic address: nstepha1@asu.edu.
Julianne L HollowayChemical Engineering, School for Engineering of Matter, Transport and Energy, Arizona State University, Tempe, AZ, United States of America; Biodesign Center for Molecular Design and Biomimetics, Arizona State University, Tempe, AZ, United States of America. Electronic address: Julianne.Holloway@asu.edu.
Arizona State University · US

Funding

Chemical synthesis of G protein-coupled receptors using sequential DNA-templated reactionsDP2GM132931 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI STEPHANOPOULOS, NICHOLAS · 2018 to 2018
$2.2M
DNA-Hyaluronic Acid Platform for Spatiotemporally Probing the Role of Adhesion Ligands on BMP-Induced Osteogenesis In VitroR21AR074069 · NIAMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI HOLLOWAY, JULIANNE LEIGH · 2019 to 2020
$348k
NIAMS NIH HHS R21 AR074069NIGMS NIH HHS DP2 GM132931
6 · The paper itself

Abstract

The extracellular matrix is a highly dynamic environment, and the precise temporal presentation of biochemical signals is critical for regulating cell behavior during development, healing, and disease progression. To mimic this behavior, we developed a modular DNA-based hydrogel platform to enable independent and reversible control over the immobilization of multiple biomolecules during in vitro cell culture. We combined reversible DNA handles with a norbornene-modified hyaluronic acid hydrogel to orthogonally add and remove multiple biomolecule-DNA conjugates at user-defined timepoints. We demonstrated that the persistent presentation of the cell adhesion peptide RGD was required to maintain cell spreading on hyaluronic acid hydrogels. Further, we discovered the delayed presentation of osteogenic growth peptide (OGP) increased alkaline phosphatase activity compared to other temporal variations. This finding is critically important when considering the design of OGP delivery approaches for bone repair. More broadly, this platform provides a unique approach to tease apart the temporal role of multiple biomolecules during development, regeneration, and disease progression.

Indexed as

Biocompatible MaterialsOsteogenesisDisease ProgressionDNAHumansHyaluronic AcidHydrogelsPeptidesBiocompatible MaterialsDNAHyaluronic AcidHydrogelsPeptidesDNAHyaluronic acidHydrogelsOsteogenesisOsteogenic growth peptideReversible biomaterials

Identifiers

PMID38096646
PMCPMC10842892
OpenAlexW4389398199

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.