In Vitro Perfused Human Capillary Networks
Open accessAbstract
Replicating in vitro the complex in vivo tissue microenvironment has the potential to transform our approach to medicine and also our understanding of biology. In order to accurately model the 3D arrangement and interaction of cells and extracellular matrix, new microphysiological systems must include a vascular supply. The vasculature not only provides the necessary convective transport of oxygen, nutrients, and waste in 3D culture, but also couples and integrates the responses of organ systems. Here we combine tissue engineering and microfluidic technology to create an in vitro 3D metabolically active stroma (∼1 mm(3)) that, for the first time, contains a perfused, living, dynamic, interconnected human capillary network. The range of flow rate (μm/s) and shear rate (s(-1)) within the network was 0-4000 and 0-1000, respectively, and thus included the normal physiological range. Infusion of FITC dextran demonstrated microvessels (15-50 μm) to be largely impermeable to 70 kDa. Our high-throughput biology-directed platform has the potential to impact a broad range of fields that intersect with the microcirculation, including tumor metastasis, drug discovery, vascular disease, and environmental chemical toxicity.
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Vascular transport is particularly required for tissues with diffusional distances greater than 200 μm.
“Indeed, vascular transport is particularly required for tissues with diffusional distances greater than 200 μm [8,182,183], and tumors are not an exception.”
From The Tumor-on-Chip: Recent Advances in the Development of Microfluidic Systems to Recapitulate the Physiology of Solid Tumors (2019) · cites this paper as [182]
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References 37 · Cited by 387
- Authors
- Moya, M. L., Hsu, Y.-H., Lee, A. P., Hughes, C. C. W., & George, S. C.
- Affiliations
- University of California, Irvine (US)
- Corresponding author
- George, Steven C.
- Venue
- Tissue Engineering Part C: Methods
- Publisher
- SAGE Publications
- Published
- 2013-09
- Volume
- 19
- Issue
- 9
- Pages
- 730-737
- ISSN
- 1937-3384 (ISSN-L)
- 1937-3392
- PMC
- PMC3719485
- OpenAlex
- W1981030985
- Cited by
- 387
- References
- 37
- Citations by year
- 2026: 12 · 2025: 17 · 2024: 30 · 2023: 27 · 2022: 26 · 2021: 44 · 2020: 34 · 2019: 28 · 2018: 36 · 2017: 34 · 2016: 37 · 2015: 21 · 2014: 24 · 2013: 15 · 2012: 1
- FWCI
- 17.85
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Tissue Engineering Part C Methods (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (F32HL105055)
- National Cancer Institute (R01CA180122, P30CA062203)
- National Institute of Environmental Health Sciences (RC1ES018361)
- Topics
- Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
- Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
- Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Capillary Electrophoresis Applications
- Keywords
- microfluidic perfusion, microcirculation, shear rate, FITC-dextran permeability, microvascular permeability, metastasis, vascular disease, drug discovery, organ-on-a-chip
- MeSH terms
- Capillaries, Computer Simulation, Dextrans, Dimethylpolysiloxanes, Humans, Microcirculation, Perfusion, Fluorescein-5-isothiocyanate, Finite Element Analysis, Microfluidics
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