Evidence map›Paper›PMID 39313990›Full record

ArticleAdvanced healthcare materials2024

Automated Microfluidics-Assisted Hydrogel-Based Wet-Spinning for the Biofabrication of Biomimetic Engineered Myotendinous Junction.

Marina Volpi, Alessia Paradiso, Ewa Walejewska, Cesare Gargioli, Marco Costantini, Wojciech Swieszkowski

Abstract read
In one paragraph

Article in Advanced healthcare materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Myotendinous Junction development and repair.Journal of orthopaedic translation · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. 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.

Marina VolpiFaculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw, 02-507, Poland.
Alessia ParadisoFaculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw, 02-507, Poland.
Ewa WalejewskaFaculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw, 02-507, Poland.
Cesare GargioliDepartment of Biology, University of Rome Tor Vergata, Rome, 00133, Italy.
Marco CostantiniInstitute of Physical Chemistry, Polish Academy of Sciences, Warsaw, 01-224, Poland.
Wojciech SwieszkowskiFaculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw, 02-507, Poland.ORCID 0000-0003-4216-9974

Funding

Narodowe Centrum Badań i Rozwoju POLTUR4/BIOCANCER/3/2021Narodowe Centrum Nauki 2018/31/D/ST8/03647Narodowe Centrum Nauki 2022/46/E/ST8/00284National Centre for Research and Developments PL-TW/VI/3/2019
6 · The paper itself

Abstract

The muscle-tendon junction (MTJ) plays a pivotal role in efficiently converting the muscular contraction into a controlled skeletal movement through the tendon. Given its complex biomechanical intricacy, the biofabrication of such tissue interface represents a significant challenge in the field of musculoskeletal tissue engineering. Herein, a novel method to produce MTJ-like hydrogel yarns using a microfluidics-assisted 3D rotary wet-spinning strategy is developed. Optimization of flow rates, rotational speed, and delivery time of bioinks enables the production of highly compartmentalized scaffolds that recapitulate the muscle, tendon, and the transient MTJ-like region. Additionally, such biofabrication parameters are validated in terms of cellular response by promoting an optimal uniaxial alignment for both muscle and tendon precursor cells. By sequentially wet-spinning C2C12 myoblasts and NIH 3T3 fibroblasts, a gradient-patterned cellular arrangement mirroring the intrinsic biological heterogeneity of the MTJ is successfully obtained. The immunofluorescence assessment further reveals the localized expression of tissue-specific markers, including myosin heavy chain and collagen type I/III, which demonstrate muscle and tenogenic tissue maturation, respectively. Remarkably, the muscle-tendon transition zone exhibits finger-like projection of the multinucleated myotubes in the tenogenic compartment, epitomizing the MTJ signature architecture.

Indexed as

HydrogelsTendonsTissue EngineeringAnimalsCell LineMiceMicrofluidicsMuscle, SkeletalMyoblastsMyotendinous JunctionNIH 3T3 CellsTissue ScaffoldsHydrogels3D bioprintingbiofabricationhydrogel fibersmicrofluidics‐assisted wet‐spinningmyotendinous junctionskeletal muscle tissue engineering

Identifiers

PMID39313990
PMCPMC11670271

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.