Cited by 49Cellular Mechanics and InteractionsTissue Engineering and Regenerative Medicine3D Printing in Biomedical Research

Controlling Major Cellular Processes of Human Mesenchymal Stem Cells using Microwell Structures

Xu, Xun, Wang, Weiwei, Kratz, Karl, Fang, Liang, Li, Zhengdong, Kurtz, Andreas, Ma, Nan, Lendlein, Andreas·2014·Advanced Healthcare Materials

Abstract

Directing stem cells towards a desired location and function by utilizing the structural cues of biomaterials is a promising approach for inducing effective tissue regeneration. Here, the cellular response of human adipose‐derived mesenchymal stem cells (hADSCs) to structural signals from microstructured substrates comprising arrays of square‐shaped or round‐shaped microwells is explored as a transitional model between 2D and 3D systems. Microwells with a side length/diameter of 50 μm show advantages over 10 μm and 25 μm microwells for accommodating hADSCs within single microwells rather than in the inter‐microwell area. The cell morphologies are three‐dimensionally modulated by the microwell structure due to differences in focal adhesion and consequent alterations of the cytoskeleton. In contrast to the substrate with 50 μm round‐shaped microwells, the substrate with 50 μm square‐shaped microwells promotes the proliferation and osteogenic differentiation potential of hADSCs but reduces the cell migration velocity and distance. Such microwell shape‐dependent modulatory effects are highly associated with Rho/ROCK signaling. Following ROCK inhibition, the differences in migration, proliferation, and osteogenesis between cells on different substrates are diminished. These results highlight the possibility to control stem cell functions through the use of structured microwells combined with the manipulation of Rho/ROCK signaling.

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Crossref · 10.1002/adhm.201400415

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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 [120]

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References 64 · Cited by 49

Authors
Xu, X., Wang, W., Kratz, K., Fang, L., Li, Z., Kurtz, A., Ma, N., & Lendlein, A.
Affiliations
  • Berlin-Brandenburger Centrum für Regenerative Therapien (DE)
  • Berlin‐Brandenburg Center for Regenerative Therapies Charité – University Medicine Berlin Augustenburger Platz 1 13353 Berlin Germany
Corresponding author
  • Ma, Nan
  • Lendlein, Andreas
Venue
Advanced Healthcare Materials
Publisher
Wiley
Published
2014-10-14
Volume
3
Issue
12
Pages
1991-2003
ISSN
  • 2192-2640 (ISSN-L)
  • 2192-2659
OpenAlex
W2091002262
Cited by
49
References
64
Citations by year
2026: 1 · 2025: 2 · 2024: 5 · 2023: 5 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 3 · 2017: 8 · 2016: 7 · 2015: 3 · 2014: 1
FWCI
3.16
Type
journal article
Language
en
Open access
closed
Locations
  • Advanced Healthcare Materials (publishedVersion)
  • PubMed (publishedVersion)
  • Seoul National University Open Repository (Seoul National University) (submittedVersion)
Funders
  • Deutsche Forschungsgemeinschaft
  • Bundesministerium für Bildung und Forschung
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
Keywords
human adipose-derived mesenchymal stem cells, microwells, microstructured substrates, structural cues, focal adhesions, cytoskeleton, cell morphology, cell proliferation, osteogenic differentiation, cell migration, Rho/ROCK signaling, ROCK inhibition, tissue regeneration
MeSH terms
Adipose Tissue, Biocompatible Materials, Cell Physiological Phenomena, Cells, Cultured, Humans, Cell Culture Techniques, Vitronectin, rho-Associated Kinases, Mesenchymal Stem Cells

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