Evidence map›Paper›PMID 42518840›Full record

ArticleRegenerative engineering and translational medicine2026

Bioprintable Janus Base Nano-Matrix for Improved Cartilage Tissue Engineering.

Leah Faber, Anne Yau, Ryan Stack, Yupeng Chen

Abstract read
In one paragraph

Article in Regenerative engineering and translational medicine, 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

4 authors.

Leah FaberDepartment of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Anne YauDepartment of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Ryan StackDepartment of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Yupeng ChenDepartment of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.ORCID 0000-0001-6940-6277

Funding

Supplement: Developing Nanomaterial Platform for Intra-Cartilage Delivery of RNA Therapeutics against Joint DiseasesR01AR072027 · NIAMS · UNIVERSITY OF CONNECTICUT STORRS · PI CHEN, YUPENG · 2017 to 2022
$2.3M
Computation-aided Molecular Design of DNA-Inspired Janus Base Biomaterials for Intracellular DeliveryR01GM155969 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI Yupeng Chen · 2024 to 2026
$1.2M
Layer-by-Layer Nano Matrix for Growth Plate RegenerationR21AR079153 · NIAMS · UNIVERSITY OF CONNECTICUT STORRS · PI CHEN, YUPENG · 2022 to 2023
$393k
NIAMS NIH HHS R01 AR072027NIAMS NIH HHS R21 AR079153NIGMS NIH HHS R01 GM155969
6 · The paper itself

Abstract

Purpose: Bioprinting is an additive manufacturing technique used to print living cells within a three-dimensional scaffold that mimics natural tissue microenvironments. There are several disadvantages to using hydrogel-based biomaterials for bioprinting including limited cell adhesion and functionality. To address this, we have developed a library of Janus base Nano-Matrices (JBNms) which are novel nanoscale scaffolds self-assembled from DNA-inspired Janus base nanotubes (JBNts) and ECM molecules. In this study, JBNms are incorporated in bioprinting by printing a cartilage-specific JBNm with human mesenchymal stem cells (hMSCs) into a 3D alginate scaffold to selectively improve chondro-lineage cell adhesion and differentiation. Methods: Human mesenchymal stem cells (hMSCs) were combined with a cartilage-specific JBNm and printed within an alginate-based bioink. They were maintained in chondrogenic media and were characterized at 7 and 28 days. Reverse transcription quantitative reverse transcriptase polymerase chain reaction (RT-qPCR) and histological staining were used to determine the presence of cartilage-specific genes and proteins. Results: The bioprinted structures with the cartilage-specific JBNm showed significantly greater expression of chondrogenic-related marker genes and glycosaminoglycan (GAG) expression after 28 days compared to the negative control group, indicating successful chondrogenesis. The cells were viable within the structures and showed significant proliferation after 28 days. Conclusion: Cartilage-specific JBNm scaffolds successfully promote enhanced hMSC adhesion, growth, and chondrogenic differentiation within bioprinted constructs.

Indexed as

BioprintingCartilage Tissue EngineeringInjectableJanus Base NanomaterialsScaffolds

Identifiers

PMID42518840
PMCPMC13384489

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Registered trials

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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.