Evidence map›Paper›PMID 24390195›Full record

ReviewJournal of biomechanical engineering2014

The role of extracellular matrix elasticity and composition in regulating the nucleus pulposus cell phenotype in the intervertebral disc: a narrative review.

Priscilla Y Hwang, Jun Chen, Liufang Jing, Brenton D Hoffman, Lori A Setton

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of biomechanical engineering, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 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

5 authors at 1 institution in 1 country.

Priscilla Y Hwang
Jun Chen
Liufang Jing
Brenton D Hoffman
Lori A Setton
Duke University · US

Funding

MECHANICAL STIMULATION OF IVD CELLSR01AR047442 · NIAMS · WASHINGTON UNIVERSITY · PI SETTON, LORI A. · 2001 to 2015
$4.6M
Genetically Designed/Tissue-Engineered Meniscal RepairR01EB002263 · NIBIB · DUKE UNIVERSITY · PI SETTON, LORI A. · 2003 to 2010
$3.2M
Developing Immature Nucleus Pulposus Cells for Regenerative TherapyR01AR057410 · NIAMS · DUKE UNIVERSITY · PI CHEN, JUN · 2009 to 2013
$1.2M
NIAMS NIH HHS AR047442NIAMS NIH HHS AR057410NIAMS NIH HHS R01 AR047442NIAMS NIH HHS R01 AR057410NIBIB NIH HHS EB002263NIBIB NIH HHS R01 EB002263
6 · The paper itself

Abstract

Intervertebral disc (IVD) disorders are a major contributor to disability and societal health care costs. Nucleus pulposus (NP) cells of the IVD exhibit changes in both phenotype and morphology with aging-related IVD degeneration that may impact the onset and progression of IVD pathology. Studies have demonstrated that immature NP cell interactions with their extracellular matrix (ECM) may be key regulators of cellular phenotype, metabolism and morphology. The objective of this article is to review our recent experience with studies of NP cell-ECM interactions that reveal how ECM cues can be manipulated to promote an immature NP cell phenotype and morphology. Findings demonstrate the importance of a soft (<700 Pa), laminin-containing ECM in regulating healthy, immature NP cells. Knowledge of NP cell-ECM interactions can be used for development of tissue engineering or cell delivery strategies to treat IVD-related disorders.

Indexed as

Models, BiologicalAnimalsCell DifferentiationComputer SimulationElastic ModulusExtracellular MatrixFibrillar CollagensFibrocartilageHumansIntervertebral DiscMechanotransduction, CellularStress, MechanicalFibrillar Collagens

Identifiers

PMID24390195
PMCPMC4023659
OpenAlexW2010775152

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.