Evidence map›Paper›PMID 42656804›Full record

ArticleBio-protocol2026

Stepwise Generation of Vascularized Multilayered 3D Organotypic Skin Models.

Haiwei Zhai, Xiaowei Jin, Meghan Biegert, Brandyn Zahs, Ruiguo Yang, Fanben Meng

Abstract read
In one paragraph

Article in Bio-protocol, 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

6 authors.

Haiwei ZhaiDepartment of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.
Xiaowei JinDepartment of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.
Meghan BiegertDepartment of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.
Brandyn ZahsDepartment of Biomedical Engineering, Michigan State University, East Lansing, MI, USA.
Ruiguo YangDepartment of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.
Fanben MengDepartment of Mechanical and Materials Engineering, University of Nebraska-Lincoln, Lincoln, NE, USA.

Funding

UNMC/EPPLEY CANCER CENTER SUPPORT GRANTP30CA036727 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI James Eudy · 1985 to 2026
$55.0M
Targeted mass spectrometry approaches to understand CART processing and recepter interactionsP20GM113126 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI GUO, JIANTAO · 2016 to 2025
$20.8M
Direct and Quantitative Probing of Desmosome MechanotransductionR35GM150623 · NIGMS · UNIVERSITY OF NEBRASKA LINCOLN · PI Ruiguo Yang · 2023 to 2026
$1.5M
NCI NIH HHS P30 CA036727NIGMS NIH HHS P20 GM113126NIGMS NIH HHS R35 GM150623
6 · The paper itself

Abstract

Skin models play critical roles in understanding disease mechanisms and advancing therapeutic development. However, conventional systems based on 2D cell cultures, in vivo animal models, and ex vivo tissue explants are limited by insufficient physiological complexity, interspecies differences, and restricted accessibility, respectively. Advances in biofabrication technologies have enabled the engineering of 3D skin equivalents that better balance biological complexity and experimental scalability. Here, we present a biofabrication protocol inspired by the regenerative processes of wound healing to construct vascularized 3D organotypic skin models in a stepwise manner. The approach integrates bioprinting for precise spatial organization of cellular compartments with guided cell self-organization to achieve native-like tissue complexity and heterogeneity. Through a programmable culture strategy, tissue maturation proceeds sequentially through keratinocyte proliferation and collective migration, microchannel endothelialization, basal-to-suprabasal differentiation, and progressive extracellular matrix remodeling within a fibrin-based scaffold. The resulting tissue constructs comprise stratified epidermal layers positioned atop a vascularized, fibroblast-remodeled dermal matrix. Beyond reproducing key structural features of human skin, this protocol recapitulates cellular processes associated with tissue regeneration, providing a dynamic platform for investigating disease pathogenesis, progression, and therapeutic responses. Key features • This protocol provides detailed procedures for preparing cells and biomaterials used in bioink formulation. • This protocol outlines a stepwise biofabrication process for integrating keratinocytes, fibroblasts, and endothelial cells into a multicellular skin model. • This protocol employs PolyJet 3D printing for tissue culture chamber fabrication and extrusion-based 3D bioprinting for spatial placement of cell-laden compartments. • This protocol leverages a dynamic, wound healing-inspired cell self-organization process under a programmable culture strategy to promote tissue maturation and architectural development.

Indexed as

BioprintingECM remodelingOrganotypic skin modelsProgrammable cultureStratified epidermisVascularization

Identifiers

PMID42656804
PMCPMC13507974

What OpenQuestion holds

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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.