Evidence map›Paper›PMID 31370352›Full record

ArticleMicromachines2019

A Milled Microdevice to Advance Glia-Mediated Therapies in the Adult Nervous System.

Juan S Peña, Denise Robles, Stephanie Zhang, Maribel Vazquez

Open access · goldAbstract read
In one paragraph

Article in Micromachines, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Re: "Organ-On-A-Chip Technologies for Advanced Blood-Retinal Barrier Models," by Ragelle et al.Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics · 2022
    Article
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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

4 authors at 2 institutions in 1 country.

Juan S PeñaDepartment of Biomedical Engineering, Rutgers, The State University of New Jersey, New Brunswick, NJ 08901, USA.
Denise RoblesDepartment of Biomedical Engineering, Rutgers, The State University of New Jersey, New Brunswick, NJ 08901, USA.
Stephanie ZhangDepartment of Biomedical Engineering, State University of New York at Binghamton, Binghamton, NY 13902, USA.
Maribel VazquezDepartment of Biomedical Engineering, Rutgers, The State University of New Jersey, New Brunswick, NJ 08901, USA. maribel.vazquez@rutgers.edu.
Rutgers, The State University of New Jersey · USBinghamton University · US

Funding

Photoreceptor integration via chemotactic honingR21EY026752 · NEI · CITY COLLEGE OF NEW YORK · PI VAZQUEZ, MARIBEL · 2016 to 2017
$431k
Foundation for the National Institutes of Health NIH R21 EY026752Foundation for the National Institutes of Health NIH SC3 GM113782NEI NIH HHS R21 EY026752
6 · The paper itself

Abstract

Neurodegenerative disorders affect millions of adults worldwide. Neuroglia have become recent therapeutic targets due to their reparative abilities in the recycling of exogenous neurotoxins and production of endogenous growth factors for proper functioning of the adult nervous system (NS). Since neuroglia respond effectively to stimuli within in vivo environments on the micron scale, adult glial physiology has remarkable synergy with microscale systems. While clinical studies have begun to explore the reparative action of Müller glia (MG) of the visual system and Schwann Cells (ShC) of the peripheral NS after neural insult, few platforms enable the study of intrinsic neuroglia responses to changes in the local microenvironment. This project developed a low-cost, benchtop-friendly microfluidic system called the glia line system, or gLL, to advance the cellular study needed for emerging glial-based therapies. The gLL was fabricated using elastomeric kits coupled with a metal mold milled via conventional computer numerical controlled (CNC) machines. Experiments used the gLL to measure the viability, adhesion, proliferation, and migration of MG and ShC within scales similar to their respective in vivo microenvironments. Results illustrate differences in neuroglia adhesion patterns and chemotactic behavior significant to advances in regenerative medicine using implants and biomaterials, as well as cell transplantation. Data showed highest survival and proliferation of MG and ShC upon laminin and illustrated a four-fold and two-fold increase of MG migration to dosage-dependent signaling from vascular endothelial growth factor (VEGF) and epidermal growth factor (EGF), respectively, as well as a 20-fold increase of ShC migration toward exogenous brain-derived neurotrophic factor (BDNF), compared to media control. The ability to quantify these biological parameters within the gLL offers an effective and reliable alternative to photolithography study neuroglia and their local ranges on the tens to hundreds of microns, using a low-cost and easily fabricated system.

Indexed as

chemotaxiscomputer numerical controlled (CNC)microfluidicsMüller glial cellsneurotrophic factorsSchwann cells

Identifiers

PMID31370352
PMCPMC6723365
OpenAlexW2965774158

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.