Evidence map›Paper›PMID 26154888›Full record

ArticleTissue engineering. Part A2015

Multivalent Conjugates of Sonic Hedgehog Accelerate Diabetic Wound Healing.

Bruce W Han, Hans Layman, Nikhil A Rode, Anthony Conway, David V Schaffer, Nancy J Boudreau, Wesley M Jackson, Kevin E Healy

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Bruce W Han1 Department of Bioengineering, University of California at Berkeley , Berkeley, California.
Hans Layman2 Department of Surgery, University of California at San Francisco , San Francisco, California.
Nikhil A Rode3 Department of Materials Science and Engineering, University of California at Berkeley , Berkeley, California.
Anthony Conway4 Department of Chemical and Biomolecular Engineering, University of California at Berkeley , Berkeley, California.
David V Schaffer1 Department of Bioengineering, University of California at Berkeley , Berkeley, California.
Nancy J Boudreau2 Department of Surgery, University of California at San Francisco , San Francisco, California.
Wesley M Jackson1 Department of Bioengineering, University of California at Berkeley , Berkeley, California.
Kevin E Healy1 Department of Bioengineering, University of California at Berkeley , Berkeley, California.
University of California, Berkeley · USUniversity of California, San Francisco · US

Funding

Multivalent Conjugates for Enhanced Bioactivity of Growth Factor Based TherapiesR21AR063940 · NIAMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HEALY, KEVIN EDWARD · 2012 to 2013
$376k
NIAMS NIH HHS R21AR063940
6 · The paper itself

Abstract

Despite their preclinical promise, few recombinant growth factors have been fully developed into effective therapies, in part, due to the short interval of therapeutic activity after administration. To address this problem, we developed nanoscale polymer conjugates for multivalent presentation of therapeutic proteins that enhance the activation of targeted cellular responses. As an example of this technology, we conjugated multiple Sonic hedgehog (Shh) proteins onto individual hyaluronic acid biopolymers to generate multivalent protein clusters at defined ratios (i.e., valencies) that yield enhanced Shh pathway activation at equivalent concentrations relative to unconjugated Shh. In this study, we investigated whether these multivalent conjugates (mvShh) could be used to improve the therapeutic function of Shh. We found that a single treatment with mvShh significantly accelerated the closure of full-thickness wounds in diabetic (db/db) mice compared to either an equivalent dose of unconjugated Shh or the vehicle control. Furthermore, we identified specific indicators of wound healing in fibroblasts and endothelial cells (i.e., transcriptional activation and cell migration) that were activated by mvShh in vitro and at concentrations approximately an order of magnitude lower than the unconjugated Shh. Taken together, our findings suggest that mvShh conjugates exhibit greater potency to activate the Shh pathway, and this multivalency advantage improves its therapeutic effect to accelerate wound closure in a diabetic animal model. Our strategy of multivalent protein presentation using nanoscale polymer conjugates has the potential to make a significant impact on the development of protein-based therapies by improving their in vivo performance.

Indexed as

AnimalsDiabetes MellitusDisease Models, AnimalHedgehog ProteinsMiceMice, Inbred C57BLNeovascularization, PhysiologicNIH 3T3 CellsSignal TransductionTime FactorsWound HealingHedgehog Proteins

Identifiers

PMID26154888
PMCPMC4554933
OpenAlexW1552490686

What OpenQuestion holds

Textmetadata
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.