Evidence map›Paper›PMID 29163881›Full record

ArticleChemical science2017

Displacement and hybridization reactions in aptamer-functionalized hydrogels for biomimetic protein release and signal transduction.

Jinping Lai, Shihui Li, Xuechen Shi, James Coyne, Nan Zhao, Fengping Dong, Yingwei Mao, Yong Wang

Abstract read
In one paragraph

Article in Chemical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Review
  2. High-fidelity ATP imagingChemical science · 2022
    Article
  3. Review
  4. Aptamer-Modified Hydrogels.Advances in biochemical engineering/biotechnology · 2021
    Article
  5. Article
  6. Review
  7. Programmable hydrogels.Biomaterials · 2018
    Review
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.

Jinping LaiDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.ORCID 0000-0001-6316-2208
Shihui LiDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.
Xuechen ShiDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.
James CoyneDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.
Nan ZhaoDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.
Fengping DongDepartment of Biology , The Pennsylvania State University , University Park 16802 , USA.
Yingwei MaoDepartment of Biology , The Pennsylvania State University , University Park 16802 , USA.
Yong WangDepartment of Biomedical Engineering , The Pennsylvania State University , University Park 16802 , USA . Email: yxw30@psu.edu.ORCID 0000-0002-2244-1742

Funding

Molecularly regulated release of angiogenic factors from superporous hydrogelsR01HL122311 · NHLBI · PENNSYLVANIA STATE UNIVERSITY, THE · PI WANG, YONG · 2015 to 2023
$4.2M
NHLBI NIH HHS R01 HL122311
6 · The paper itself

Abstract

A variety of hydrogels have been synthesized for controlling the release of signaling molecules in applications such as drug delivery and regenerative medicine. However, it remains challenging to synthesize hydrogels with the ability to control the release of signaling molecules sequentially or periodically under physiological conditions as living cells do in response to the variation of metabolism. The purpose of this work was to study a novel biomimetic hydrogel system with the ability of recapitulating the procedure of cellular signal transduction and controlling the sequential release of signaling molecules under physiological conditions. In the presence of a small chemical, the signaling molecule is regulated to change from a DNA-bound state to a free state and the freed signaling molecule is able to regulate intracellular signal transduction and cell migration. Moreover, periodic exposure of the hydrogel system to the small chemical leads to sequential protein release. Since signaling molecules are important for every activity of the cell, this hydrogel system holds potential as a metabolism-responsive platform for controlled release of signaling molecules and cell regulation in various applications.

Identifiers

PMID29163881
PMCPMC5672785

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.