Cited by 2973D Printing in Biomedical ResearchLiver physiology and pathologyTissue Engineering and Regenerative Medicine

Spheroid-based three-dimensional liver-on-a-chip to investigate hepatocyte–hepatic stellate cell interactions and flow effects

Lee, Seung-A, No, Da Yoon, Kang, Edward, Ju, Jongil, Kim, Dong-Sik, Lee, Sang-Hoon·2013·Lab on a Chip

Abstract

We have developed a three-dimensional (3D) liver-on-a-chip to investigate the interaction of hepatocytes and hepatic stellate cells (HSCs) in which primary 3D hepatocyte spheroids and HSCs are co-cultured without direct cell-cell contact. Here, we show that the 3D liver chip offers substantial advantages for the formation and harvesting of spheroids. The most important feature of this liver chip is that it enables continuous flow of medium to the cells through osmotic pumping, and thus requires only minimal handling and no external power source. We also demonstrate that flow assists the formation and long-term maintenance of spheroids. Additionally, we quantitatively and qualitatively investigated the paracrine effects of HSCs, demonstrating that HSCs assist in the maintenance of hepatocyte spheroids and play an important role in the formation of tight cell-cell contacts, thereby improving liver-specific function. Spheroids derived from co-cultures exhibited improved albumin and urea secretion rates compared to mono-cultured spheroids after 9 days. Immunostaining for cytochrome P450 revealed that the enzymatic activity of spheroids co-cultured for 8 days was greater than that of mono-cultured spheroids. These results indicate that this system has the potential for further development as a unique model for studying cellular interactions or as a tool that can be incorporated into other models aimed at creating hepatic structure and prolonging hepatocyte function in culture.

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Crossref · 10.1039/c3lc50197c

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  • Spheroid cell culture has been developed for research on cancer, stem cells, and many organs, including liver, kidney, and heart.

    “This approach has been developed in the research of cancer (7, 76, 102), stem cells (17, 120), and many organs (such as liver, kidney, heart, etc.) (3,16,64,75).”

    From Modeling physiological events in 2D vs. 3D cell culture (2017) · cites this paper as [75]

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References 48 · Cited by 297

Authors
Lee, S.-A., No, D. Y., Kang, E., Ju, J., Kim, D.-S., & Lee, S.-H.
Affiliations
Korea University (KR)
Corresponding author
Lee, Sang-Hoon
Venue
Lab on a Chip
Published
2013
Volume
13
Issue
18
Pages
3529
ISSN
  • 1473-0189 (ISSN-L)
  • 1473-0197
OpenAlex
W2058794699
Cited by
297
References
48
Citations by year
2026: 9 · 2025: 12 · 2024: 24 · 2023: 19 · 2022: 29 · 2021: 14 · 2020: 27 · 2019: 41 · 2018: 28 · 2017: 27 · 2016: 22 · 2015: 19 · 2014: 20 · 2013: 6
FWCI
12.30
Type
journal article
Language
en
Open access
closed
Locations
  • Lab on a Chip (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
  • Health Sciences › Medicine › Hepatology › Liver physiology and pathology
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
Keywords
liver-on-a-chip, hepatocyte spheroids, hepatic stellate cells, co-culture, spheroid formation, paracrine signaling, cell-cell contact, albumin secretion, urea secretion, cytochrome P450 activity, liver tissue engineering
MeSH terms
Albumins, Animals, Cells, Cultured, Cytochrome P-450 Enzyme System, Male, Urea, Rats, Sprague-Dawley, Spheroids, Cellular, Coculture Techniques, Cell Culture Techniques, Paracrine Communication, Hepatocytes, Microfluidic Analytical Techniques, Rats, Hepatic Stellate Cells

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