Evidence map›Paper›PMID 26874887›Full record

ArticleBiomaterials2016

Spatiotemporal control of cardiac anisotropy using dynamic nanotopographic cues.

Paulos Y Mengsteab, Koichiro Uto, Alec S T Smith, Sam Frankel, Elliot Fisher, Zeid Nawas, Jesse Macadangdang, Mitsuhiro Ebara, Deok-Ho Kim

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.5field-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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Engineering Multi-Scale Organization for Biotic and Organic Abiotic Electroactive Systems.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  4. Review
  5. Engineering Three-Dimensional Vascularized Cardiac Tissues.Tissue engineering. Part B, Reviews · 2022
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Micro- and nanoscale biophysical cues for cardiovascular disease therapy.Nanomedicine : nanotechnology, biology, and medicine · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Applications of Bioengineered 3D Tissue and Tumor Organoids in Drug Development and Precision Medicine: Current and Future.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2018
    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

9 authors at 2 institutions in 2 countries.

Paulos Y MengsteabDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Koichiro UtoDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA; International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.
Alec S T SmithDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Sam FrankelDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Elliot FisherDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Zeid NawasDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Jesse MacadangdangDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Mitsuhiro EbaraInternational Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.
Deok-Ho KimDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA; Center for Cardiovascular Biology, University of Washington, Seattle, WA 98109, USA. Electronic address: deokho@uw.edu.
University of Washington · USNational Institute for Materials Science · JP

Funding

EXPERIMENTAL PATHOLOGY OF CARDIOVASCULAR DISEASET32HL007312 · NHLBI · UNIVERSITY OF WASHINGTON · PI MAJESKY, MARK W., SCHWARTZ, STEPHEN MARK · 1985 to 2019
$11.8M
UW Post-Baccalaureate Research Education Program (PREP)R25GM086304 · NIGMS · UNIVERSITY OF WASHINGTON · PI Gabriele Varani · 2011 to 2026
$5.7M
NHLBI NIH HHS 2T32HL007312-36A1NHLBI NIH HHS T32 HL007312NIGMS NIH HHS 2R25GM086304NIGMS NIH HHS R25 GM086304
6 · The paper itself

Abstract

Coordinated extracellular matrix spatiotemporal reorganization helps regulate cellular differentiation, maturation, and function in vivo, and is therefore vital for the correct formation, maintenance, and healing of complex anatomic structures. In order to evaluate the potential for cultured cells to respond to dynamic changes in their in vitro microenvironment, as they do in vivo, the collective behavior of primary cardiac muscle cells cultured on nanofabricated substrates with controllable anisotropic topographies was studied. A thermally induced shape memory polymer (SMP) was employed to assess the effects of a 90° transition in substrate pattern orientation on the contractile direction and structural organization of cardiomyocyte sheets. Cardiomyocyte sheets cultured on SMPs exhibited anisotropic contractions before shape transition. 48 h after heat-induced shape transition, the direction of cardiomyocyte contraction reoriented significantly and exhibited a bimodal distribution, with peaks at ∼45 and -45° (P < 0.001). Immunocytochemical analysis highlighted the significant structural changes that the cells underwent in response to the shift in underlying topography. The presented results demonstrate that initial anisotropic nanotopographic cues do not permanently determine the organizational fate or contractile properties of cardiomyocytes in culture. Given the importance of surface cues in regulating primary and stem cell development, investigation of such tunable nanotopographies may have important implications for advancing cellular maturation and performance in vitro, as well as improving our understanding of cellular development in response to dynamic biophysical cues.

Indexed as

AnimalsAnisotropyBiocompatible MaterialsCells, CulturedMyocardial ContractionMyocytes, CardiacNanostructuresPolyestersRats, Sprague-DawleyTemperatureTissue EngineeringTransition TemperatureBiocompatible MaterialspolycaprolactonePolyestersCardiomyocyteContractile anisotropyECMNanotopographyShape memory polymers

Identifiers

PMID26874887
PMCPMC4775380
OpenAlexW2297402083

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.