Evidence map›Paper›PMID 27645115›Full record

ArticleMatrix biology : journal of the International Society for Matrix Biology2017

Hyaluronic acid-laminin hydrogels increase neural stem cell transplant retention and migratory response to SDF-1α.

C P Addington, S Dharmawaj, J M Heffernan, R W Sirianni, S E Stabenfeldt

Abstract read
In one paragraph

Article in Matrix biology : journal of the International Society for Matrix Biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 52 citations in OpenAlex.

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  8. Stem Cell- and Cell-Based Therapies for Ischemic Stroke.Bioengineering (Basel, Switzerland) · 2022
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  20. Distinct roles for hyaluronan in neural stem cell niches and perineuronal nets.Matrix biology : journal of the International Society for Matrix Biology · 2019
    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

5 authors at 3 institutions in 1 country.

C P AddingtonSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, United States.
S DharmawajDepartment of Biomedical Engineering, New Jersey Institute of Technology, Newark, NJ, United States.
J M HeffernanSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, United States; Barrow Brain Tumor Research Center, Barrow Neurological Institute, Phoenix, AZ, United States.
R W SirianniSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, United States; Barrow Brain Tumor Research Center, Barrow Neurological Institute, Phoenix, AZ, United States.
S E StabenfeldtSchool of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ, United States. Electronic address: sarah.stabenfeldt@asu.edu.
Arizona State University · USBarrow Neurological Institute · USNew Jersey Institute of Technology · US

Funding

Detecting and Treating Traumatic Brain Injury Pathology Progression from the Inside-OutDP2HD084067 · NICHD · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI STABENFELDT, SARAH E · 2014 to 2018
$2.8M
NICHD NIH HHS DP2 HD084067
6 · The paper itself

Abstract

The chemokine SDF-1α plays a critical role in mediating stem cell response to injury and disease and has specifically been shown to mobilize neural progenitor/stem cells (NPSCs) towards sites of neural injury. Current neural transplant paradigms within the brain suffer from low rates of retention and engraftment after injury. Therefore, increasing transplant sensitivity to injury-induced SDF-1α represents a method for increasing neural transplant efficacy. Previously, we have reported on a hyaluronic acid-laminin based hydrogel (HA-Lm gel) that increases NPSC expression of SDF-1α receptor, CXCR4, and subsequently, NPSC chemotactic migration towards a source of SDF-1α in vitro. The study presented here investigates the capacity of the HA-Lm gel to promote NPSC response to exogenous SDF-1α in vivo. We observed the HA-Lm gel to significantly increase NPSC transplant retention and migration in response to SDF-1α in a manner critically dependent on signaling via the SDF-1α-CXCR4 axis. This work lays the foundation for development of a more effective cell therapy for neural injury, but also has broader implications in the fields of tissue engineering and regenerative medicine given the essential roles of SDF-1α across injury and disease states.

Indexed as

Stem Cell TransplantationAnimalsBrainBrain InjuriesCell- and Tissue-Based TherapyCell MovementChemokine CXCL12Embryo, MammalianGene ExpressionHyaluronic AcidHydrogelsInjections, IntraventricularLamininMaleMiceMice, Inbred C57BLChemokine CXCL12CXCR4 protein, mouseHyaluronic AcidHydrogelsLamininReceptors, CXCR4BiomaterialsChemotaxisCXCL12Neural progenitor cellsRegenerative medicineTissue engineering

Identifiers

PMID27645115
PMCPMC5357205
OpenAlexW2520522924

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.