Effect of Serum on Smooth Muscle Cell Phenotype in 3D Tissue-Engineered Microvessels

Smooth muscle cells (SMCs) are a critical cellular component of the tunica media of blood vessels in arteries and arterioles. Despite their importance, the development of in vitro arteriole models with diameters <200 µm remains challenging, largely due to difficulties in culturing SMCs at these length scales. In particular, uncontrolled SMC overproliferation can lead to microvessel vessel narrowing and occlusion. Here, we report a 3D microfluidic-based tissue-engineered model with human brain SMCs forming a microvessel approximately 150 μm in diameter within a collagen I hydrogel. Using this platform, we demonstrate that serum-free culture conditions are essential to prevent SMC overproliferation and maintain vessel patency. In addition, SMCs cultured in serum-free and serum-supplemented conditions exhibit distinct functional phenotypes, consistent with previous studies in 2D culture. These results provide a strategy for fabrication of tissue-engineered arteriole models.

Authors

Institutions

Publication Details

Journal
ACS Biomaterials Science & Engineering
Published
2026-10-13
DOI
https://doi.org/10.1021/acsbiomaterials.6c01600
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effect of Serum on Smooth Muscle Cell Phenotype in 3D Tissue-Engineered Microvessels

Peter C. Searson, Lily Rui Liang, Ninghao Zhu, Yunhan Liao
ACS Biomaterials Science & Engineering
3D Printing in Biomedical Research
article

Effect of Serum on Smooth Muscle Cell Phenotype in 3D Tissue-Engineered Microvessels

Peter C. Searson, Lily Rui Liang, Ninghao Zhu, Yunhan Liao
article en

Abstract

Smooth muscle cells (SMCs) are a critical cellular component of the tunica media of blood vessels in arteries and arterioles. Despite their importance, the development of in vitro arteriole models with diameters <200 µm remains challenging, largely due to difficulties in culturing SMCs at these length scales. In particular, uncontrolled SMC overproliferation can lead to microvessel vessel narrowing and occlusion. Here, we report a 3D microfluidic-based tissue-engineered model with human brain SMCs forming a microvessel approximately 150 μm in diameter within a collagen I hydrogel. Using this platform, we demonstrate that serum-free culture conditions are essential to prevent SMC overproliferation and maintain vessel patency. In addition, SMCs cultured in serum-free and serum-supplemented conditions exhibit distinct functional phenotypes, consistent with previous studies in 2D culture. These results provide a strategy for fabrication of tissue-engineered arteriole models.

ACS Biomaterials Science & Engineering
Johns Hopkins University (US), SUNY Plattsburgh (US)
National Heart, Lung, and Blood Institute, National Eye Institute, National Science Foundation Graduate Research Fellowship Program
Openalex Percentile: Top 24%
3D Printing in Biomedical Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.