Evidence map›Paper›PMID 32654327›Full record

ArticleJournal of biomedical materials research. Part A2021

A multilayered scaffold for regeneration of smooth muscle and connective tissue layers.

Carly M Garrison, Anya Singh-Varma, Alexandra K Pastino, Joseph A M Steele, Joachim Kohn, N Sanjeeva Murthy, Jean E Schwarzbauer

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

7 authors at 2 institutions in 1 country.

Carly M GarrisonDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, USA.
Anya Singh-VarmaDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, USA.
Alexandra K PastinoNew Jersey Center for Biomaterials, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Joseph A M SteeleNew Jersey Center for Biomaterials, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Joachim KohnNew Jersey Center for Biomaterials, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
N Sanjeeva MurthyNew Jersey Center for Biomaterials, Rutgers, The State University of New Jersey, Piscataway, New Jersey, USA.
Jean E SchwarzbauerDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, USA.
Rutgers, The State University of New Jersey · USPrinceton University · US

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007388 · NIGMS · PRINCETON UNIVERSITY · PI CRISTEA, ILEANA M. · 1985 to 2022
$27.4M
RESBIO - the Technology Resource for Polymeric BiomaterialsP41EB001046 · NIBIB · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI KOHN, JOACHIM B. · 2003 to 2017
$17.0M
Fibronectin-dependent mechanisms governing the assembly of a definitive extracellular matrixR01AR073236 · NIAMS · PRINCETON UNIVERSITY · PI SCHWARZBAUER, JEAN E · 2018 to 2022
$1.7M
NIAMS NIH HHS R01 AR073236NIBIB NIH HHS P41 EB001046NIGMS NIH HHS T32 GM007388
6 · The paper itself

Abstract

Tissue regeneration often requires recruitment of different cell types and rebuilding of two or more tissue layers to restore function. Here, we describe the creation of a novel multilayered scaffold with distinct fiber organizations-aligned to unaligned and dense to porous-to template common architectures found in adjacent tissue layers. Electrospun scaffolds were fabricated using a biodegradable, tyrosine-derived terpolymer, yielding densely-packed, aligned fibers that transition into randomly-oriented fibers of increasing diameter and porosity. We demonstrate that differently-oriented scaffold fibers direct cell and extracellular matrix (ECM) organization, and that scaffold fibers and ECM protein networks are maintained after decellularization. Smooth muscle and connective tissue layers are frequently adjacent in vivo; we show that within a single scaffold, the architecture supports alignment of contractile smooth muscle cells and deposition by fibroblasts of a meshwork of ECM fibrils. We rolled a flat scaffold into a tubular construct and, after culture, showed cell viability, orientation, and tissue-specific protein expression in the tube were similar to the flat-sheet scaffold. This scaffold design not only has translational potential for reparation of flat and tubular tissue layers but can also be customized for alternative applications by introducing two or more cell types in different combinations.

Indexed as

PolymersTissue Scaffolds3T3 CellsAnimalsCell MovementCells, CulturedConnective TissueFibroblastsHumansMaterials TestingMiceMyocytes, Smooth MusclePhenotypePorosityRatsRats, Inbred WKYE1001(1k)PolymersTyrosinecomplex tissue regenerationextracellular matrix (ECM)multilayered electrospun scaffoldssynthetic polymertubular scaffold

Identifiers

PMID32654327
PMCPMC7855544
OpenAlexW3041439435

What OpenQuestion holds

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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.