Evidence map›Paper›PMID 27516731›Full record

ArticleAdvanced functional materials2015

Protein Corona Influences Cell-Biomaterial Interactions in Nanostructured Tissue Engineering Scaffolds.

Vahid Serpooshan, Morteza Mahmoudi, Mingming Zhao, Ke Wei, Senthilkumar Sivanesan, Khatereh Motamedchaboki, Andrey V Malkovskiy, Andrew B Gladstone, Jeffrey E Cohen, Phillip C Yang and 4 more

Abstract read
In one paragraph

Article in Advanced functional materials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 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

14 authors at 3 institutions in 1 country.

Vahid Serpooshan *Stanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Morteza Mahmoudi *Stanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Mingming ZhaoDepartment of Pediatrics, Stanford University, 300 Pasteur Dr., Stanford, CA 94305.
Ke WeiSanford-Burnham Medical Research Institute, 10901 N. Torrey Pines Road, La Jolla, CA, 92037.
Senthilkumar SivanesanBiomaterials and Advanced Drug Delivery Laboratory, Stanford University, 300 Pasteur Dr., Stanford, CA 94305.
Khatereh MotamedchabokiProteomics Facility, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037.
Andrey V MalkovskiyBiomaterials and Advanced Drug Delivery Laboratory, Stanford University, 300 Pasteur Dr., Stanford, CA 94305.
Andrew B GladstoneDepartment of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, CA 94305.
Jeffrey E CohenDepartment of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, CA 94305.
Phillip C YangStanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Jayakumar RajadasStanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Daniel BernsteinStanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Y Joseph WooDepartment of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, CA 94305.
Pilar Ruiz-LozanoStanford Cardiovascular Institute, Stanford, CA, 94305 USA.
Stanford University · USCardiovascular Institute of the South · USSanford Burnham Prebys Medical Discovery Institute · US

Funding

GENETIC ABLATION OF EPICARDIAL FUNCTION IN THE MOUSER01HL065484 · NHLBI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI RUIZ-LOZANO, PILAR · 2002 to 2012
$3.7M
ROLE OF BETA-RECEPTOR SIGNALING IN CARDIOMYOPATHYR01HL061535 · NHLBI · STANFORD UNIVERSITY · PI BERNSTEIN, DANIEL · 2000 to 2010
$3.3M
Integrated Strategies for Novel Treatment of Myocardial IschemiaR01HL095571 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2010 to 2014
$2.0M
Genetic Rescue of Retinoid-Induced DysfunctionR01HL086879 · NHLBI · STANFORD UNIVERSITY · PI RUIZ-LOZANO, PILAR · 2009 to 2013
$1.7M
Genetic Ablation of Epicardial Function in the MouseR56HL065484 · NHLBI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI RUIZ-LOZANO, PILAR · 2007 to 2007
$478k
NHLBI NIH HHS R01 HL061535NHLBI NIH HHS R01 HL065484NHLBI NIH HHS R01 HL086879NHLBI NIH HHS R01 HL095571NHLBI NIH HHS R56 HL065484
6 · The paper itself

Abstract

Biomaterials are extensively used to restore damaged tissues, in the forms of implants (e.g. tissue engineered scaffolds) or biomedical devices (e.g. pacemakers). Once in contact with the physiological environment, nanostructured biomaterials undergo modifications as a result of endogenous proteins binding to their surface. The formation of this macromolecular coating complex, known as 'protein corona', onto the surface of nanoparticles and its effect on cell-particle interactions are currently under intense investigation. In striking contrast, protein corona constructs within nanostructured porous tissue engineering scaffolds remain poorly characterized. As organismal systems are highly dynamic, it is conceivable that the formation of distinct protein corona on implanted scaffolds might itself modulate cell-extracellular matrix interactions. Here, we report that corona complexes formed onto the fibrils of engineered collagen scaffolds display specific, distinct, and reproducible compositions that are a signature of the tissue microenvironment as well as being indicative of the subject's health condition. Protein corona formed on collagen matrices modulated cellular secretome in a context-specific manner

Indexed as

collagenin situ biosensorpersonalized nanostructured biomaterialsprotein coronatissue engineering scaffold

Identifiers

PMID27516731
PMCPMC4978190
OpenAlexW1835697155

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.