Evidence map›Paper›PMID 41492643›Full record

ArticleMaterials today. Bio2026

Melt-electrowriting fibrous scaffolds modified with nano-topography structures promoting cardiomyocytes synergistic contraction.

Jinqiao Jia, Qi Lei, Xiumei Zhang, Xiaomin Guan, Zhengjiang Liu, Jiapu Wang, Shilei Zhu, Ya Nan Ye, Di Huang

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jinqiao JiaCollege of Materials Science & Engineering, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Qi LeiDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Xiumei ZhangDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Xiaomin GuanDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Zhengjiang LiuDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Jiapu WangDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Shilei ZhuCollege of Materials Science & Engineering, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Ya Nan YeCollege of Materials Science & Engineering, Taiyuan University of Technology, Taiyuan, 030024, PR China.
Di HuangDepartment of Biomedical Engineering, Research Center for Nano-biomaterials & Regenerative Medicine, Shanxi Key Laboratory of Functional Proteins, College of Artificial Intelligence, Taiyuan University of Technology, Taiyuan, 030024, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melt-electrowriting (MEW) is an emerging strategy to fabricate microfibrous scaffolds that mimic the functional collagen fibers present in the native extracellular matrix (ECM). However, the main challenge remains in producing the nanoscale features that are widely found in ECM. In this work, MEW polycaprolactone (PCL) fibrous scaffolds with nano-topography structures (NS) were prepared to promote cell growth. Parallel PCL fibers were coated with NS by self-induced crystallization, which enhanced the adhesion and spreading of H9C2 cells. Compared with pristine scaffolds, the NS scaffolds exhibited improved hydrophilicity with a lower water contact angle of ∼50.70°. NS scaffolds exhibited abundant nano sites, which are beneficial for the cell-scaffold interaction and for achieving living constructs at a high cell density. Furthermore, NS scaffolds promoted cell-cell interactions and synergistic contraction of neonatal mouse cardiomyocytes (CMs). Dendritic pseudopods enabled CMs to spread along preferentially parallel to the direction of the lamellar. RNA sequencing analyses further revealed that the NS scaffolds upregulate cell cycle regulation-related pathways, cell communication-related pathways, calcium regulation-related pathways, cell motility-related pathways, and cellular adhesion and spreading-related pathways. It is envisioned that the proposed NS scaffolds may serve as promising candidates for tissue regeneration and biomedical engineering applications.

Indexed as

Gene expressionMelt-electrowritingMicrofibrous scaffoldsNano-topography structuresSynergistic contraction

Identifiers

PMID41492643
PMCPMC12765063

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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.