Evidence map›Paper›PMID 25143513›Full record

ArticleJournal of dental research2014

Multi-lineage MSC differentiation via engineered morphogen fields.

P R Arany, G X Huang, O Gadish, J Feliz, J C Weaver, J Kim, W W Yuen, D J Mooney

Abstract read
In one paragraph

Article in Journal of dental research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

8 authors.

P R AranyHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA Harvard School of Dental Medicine, Boston, MA, USA National Institute of Dental and Craniofacial Research, Bethesda, MD, USA.
G X HuangHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA.
O GadishHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA.
J FelizHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA.
J C WeaverWyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA.
J KimHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA School of Chemical Engineering, Sungkyunkwan University, Suwon 440-746, Republic of Korea.
W W YuenHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA.
D J MooneyHarvard School of Engineering and Applied Sciences, Cambridge, MA, USA Wyss Institute for Biologically Inspired Engineering, Harvard University, Cambridge, MA, USA mooneyd@seas.harvard.edu.

Funding

Polymeric Matrices with Defined Cell AdhesionR37DE013033 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOONEY, DAVID J · 2004 to 2013
$3.8M
POLYMERIC MATRICES WITH DEFINED CELL ADHESION AND MECHANR01DE013033 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOONEY, DAVID J · 1998 to 2018
$3.0M
Oral Wound HealingZIADE000741 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI ARANY, PRAVEEN · 2013 to 2015
$2.0M
NIDCR NIH HHS R01 DE013033NIDCR NIH HHS R37 DE013033NIDCR NIH HHS R37DE013033
6 · The paper itself

Abstract

Tissue loss due to oral diseases requires the healing and regeneration of tissues of multiple lineages. While stem cells are native to oral tissues, a current major limitation to regeneration is the ability to direct their lineage-specific differentiation. This work utilizes polymeric scaffold systems with spatiotemporally controlled morphogen cues to develop precise morphogen fields to direct mesenchymal stem cell differentiation. First, a simple three-layer scaffold design was developed that presented two spatially segregated, lineage-specific cues (Dentinogenic TGF-β1 and Osteogenic BMP4). However, this system resulted in diffuse morphogen fields, as assessed by the in vitro imaging of cell-signaling pathways triggered by the morphogens. Mathematical modeling was then exploited, in combination with incorporation of specific inhibitors (neutralizing antibodies or a small molecule kinase inhibitor) into each morphogen in an opposing spatial pattern as the respective morphogen, to design a five-layer scaffold that was predicted to yield distinct, spatially segregated zones of morphogen signaling. To validate this system, undifferentiated MSCs were uniformly seeded in these scaffold systems, and distinct mineralized tissue differentiation were noted within these morphogen zones. Finally, to demonstrate temporal control over morphogen signaling, latent TGF-β1 was incorporated into one region of a concentric scaffold design, and laser treatment was used to activate the morphogen on-demand and to induce dentin differentiation solely within that specific spatial zone. This study demonstrates a significant advance in scaffold design to generate precise morphogen fields that can be used to develop in situ models to explore tissue differentiation and may ultimately be useful in engineering multi-lineage tissues in clinical dentistry.

Indexed as

AnimalsBone Morphogenetic Protein 4Cell Culture TechniquesCell DifferentiationCell LineageDentinogenesisDiffusionHumansIntercellular Signaling Peptides and ProteinsLactic AcidLasers, SemiconductorMesenchymal Stem CellsMiceModels, BiologicalOsteogenesisParacrine CommunicationBMP4 protein, humanBone Morphogenetic Protein 4Intercellular Signaling Peptides and ProteinsLactic AcidPolyglycolic AcidPolylactic Acid-Polyglycolic Acid CopolymerTransforming Growth Factor beta1dentinogenesisdirected differentiationgrowth factorsosteogenesisscaffoldsTGF-beta1

Identifiers

PMID25143513
PMCPMC4237631

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.