Evidence map›Paper›PMID 40127539›Full record

ArticleBiofabrication2025

Cellnet technology to generate 3D, functional, single-cell networks in custom architectures within collagen.

Arun Poudel, Puskal Kunwar, Ujjwal Aryal, Anna-Blessing Merife, Pranav Soman

Abstract read
In one paragraph

Article in Biofabrication, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Rethinking osteocyte modelsFrontiers in bioengineering and biotechnology · 2026
    Review
  5. 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

5 authors.

Arun PoudelDepartment of Chemical and Biomedical Engineering and BioInspired Institute, Syracuse University, Syracuse, NY 13210, United States of America.ORCID 0000-0003-4899-7594
Puskal KunwarDepartment of Chemical and Biomedical Engineering and BioInspired Institute, Syracuse University, Syracuse, NY 13210, United States of America.
Ujjwal AryalDepartment of Chemical and Biomedical Engineering and BioInspired Institute, Syracuse University, Syracuse, NY 13210, United States of America.
Anna-Blessing MerifeDepartment of Chemical and Biomedical Engineering and BioInspired Institute, Syracuse University, Syracuse, NY 13210, United States of America.
Pranav SomanDepartment of Chemical and Biomedical Engineering and BioInspired Institute, Syracuse University, Syracuse, NY 13210, United States of America.ORCID 0000-0001-9456-0030

Funding

Role of Ca2+ Signaling by 3D Osteocyte Networks in Mechanoadaptive Response of the Bone Multicellular UnitR01AR083466 · NIAMS · SYRACUSE UNIVERSITY · PI Pranav Soman · 2024 to 2026
$943k
Design of the Glomerulus and bOwman cApsuLe on a chip (GOAL)R21DK136083 · NIDDK · UPSTATE MEDICAL UNIVERSITY · PI KRENDEL, MIRA · 2023 to 2023
$435k
NIAMS NIH HHS R01 AR083466NIDDK NIH HHS R21 DK136083
6 · The paper itself

Abstract

Cells possess the remarkable ability to generate tissue-specific 3D interconnected networks and respond to a wide range of stimuli. Understanding the link between the spatial arrangement of individual cells and their networks' emergent properties is necessary for the discovery of both fundamental biology as well as applied therapeutics. However, current methods spanning from lithography to 3D photo-patterning to acoustofluidic devices are unable to generate interconnected and organized single cell 3D networks within native extracellular matrix (ECM). To address this challenge, we report a novel technology coined as Cellnet. This involves the use of natural collagen crosslinked within three-chambered microfluidic chips followed by femtosecond laser-assisted cavitation to generate user-defined 3D microchannel networks. Model cells, seeded within side chamber of the chip, migrate within microchannel networks within hours, self-organize and form viable, interconnected, 3D single-cell networks in custom architectures such as square grid, concentric circle, parallel lines, and spiral patterns. Heterotypic Cellnets can also be generated by seeding multiple cell types in side-chambers of the chip. The functionality of cell networks can be studied by monitoring the real-time calcium signaling response of individual cells and signal propagation within Cellnets when subjected to flow stimulus alone or a sequential combination of flow and biochemical stimuli. Furthermore, user-defined disrupted Cellnets can be generated by lethally injuring target cells within the 3D network and analyzing the changes in their signaling dynamics. As compared to the current self-assembly based methods that exhibit high variability and poor reproducibility, Cellnets can generate organized 3D single-cell networks and their real-time signaling responses to a range of stimuli can be accurately captured using simple cell seeding and easy-to-handle microfluidic chips. Cellnet technology, agnostic of cell types, ECM formulations, 3D cell-connectivity designs, or location and timing of network disruptions, could pave the way to address a range of fundamental and applied bioscience applications.

Indexed as

Cell Culture Techniques, Three DimensionalCollagenSingle-Cell AnalysisTissue EngineeringAnimalsExtracellular MatrixHumansLab-On-A-Chip DevicesMiceCollagen3DCELLNETfunctionalorganizedspatiallytechnology

Identifiers

PMID40127539
PMCPMC11966782

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.