Evidence map›Paper›PMID 31624124›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Living myofibroblast-silicon composites for probing electrical coupling in cardiac systems.

Menahem Y Rotenberg, Naomi Yamamoto, Erik N Schaumann, Laura Matino, Francesca Santoro, Bozhi Tian

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Hydrogel-based neural engineering for skin wound healing.Frontiers in cell and developmental biology · 2026
    Review
  2. Article
  3. Article
  4. Generation and applications of cardiac spheroids.npj biomedical innovations · 2025
    Review
  5. Article
  6. Article
  7. Advances in cardiac tissue engineering and heart-on-a-chip.Journal of biomedical materials research. Part A · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Nanoenabled Bioelectrical Modulation.Accounts of materials research · 2021
    Article
  15. Review
  16. Recent advances in bioelectronics chemistry.Chemical Society reviews · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

6 authors.

Menahem Y RotenbergThe James Franck Institute, The University of Chicago, Chicago, IL 60637; hrotenberg@uchicago.edu btian@uchicago.edu.
Naomi YamamotoDepartment of Chemistry, The University of Chicago, Chicago, IL 60637.
Erik N SchaumannDepartment of Chemistry, The University of Chicago, Chicago, IL 60637.
Laura MatinoTissue Electronics, Center for Advanced Biomaterials for Healthcare, Istituto Italiano di Tecnologia, 80125 Naples, Italy.
Francesca SantoroTissue Electronics, Center for Advanced Biomaterials for Healthcare, Istituto Italiano di Tecnologia, 80125 Naples, Italy.
Bozhi TianThe James Franck Institute, The University of Chicago, Chicago, IL 60637; hrotenberg@uchicago.edu btian@uchicago.edu.ORCID 0000-0003-0593-0023

Funding

Silicon-based Injectable Micro-gels for Non-genetic and Wireless Modulation of Neurons, Cardiomyocytes and Neuromuscular SystemDP2NS101488 · NINDS · UNIVERSITY OF CHICAGO · PI TIAN, BOZHI · 2016 to 2016
$2.4M
NINDS NIH HHS DP2 NS101488
6 · The paper itself

Abstract

Traditional bioelectronics, primarily comprised of nonliving synthetic materials, lack cellular behaviors such as adaptability and motility. This shortcoming results in mechanically invasive devices and nonnatural signal transduction across cells and tissues. Moreover, resolving heterocellular electrical communication in vivo is extremely limited due to the invasiveness of traditional interconnected electrical probes. In this paper, we present a cell-silicon hybrid that integrates native cellular behavior (e.g., gap junction formation and biosignal processing) with nongenetically enabled photosensitivity. This hybrid configuration allows interconnect-free cellular modulation with subcellular spatial resolution for bioelectric studies. Specifically, we hybridize cardiac myofibroblasts with silicon nanowires and use these engineered hybrids to synchronize the electrical activity of cardiomyocytes, studying heterocellular bioelectric coupling in vitro. Thereafter, we inject the engineered myofibroblasts into heart tissues and show their ability to seamlessly integrate into contractile tissues in vivo. Finally, we apply local photostimulation with high cell specificity to tackle a long-standing debate regarding the existence of myofibroblast-cardiomyocyte electrical coupling in vivo.

Indexed as

AnimalsBioengineeringCells, CulturedElectrophysiological PhenomenaGap JunctionsHumansMiceMyocytes, CardiacMyofibroblastsNanowiresSignal TransductionSiliconSiliconcardiomyocyteselectrical couplingmyofibroblastoptical stimulationsilicon nanowires

Identifiers

PMID31624124
PMCPMC6842627

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.