Self-assembling proteins as high-performance substrates for embryonic stem cell self-renewal
Abstract
The development of extracellular matrix mimetics that imitate niche stem cell microenvironments and support cell growth for technological applications is intensely pursued. Specifically, mimetics are sought that can enact control over the self‐renewal and directed differentiation of human pluripotent stem cells (hPSCs) for clinical use. Despite considerable progress in the field, a major impediment to the clinical translation of hPSCs is the difficulty and high cost of large‐scale cell production under xeno‐free culture conditions using current matrices. Here, a bioactive, recombinant, protein‐based polymer, termed ZT Fn , is presented that closely mimics human plasma fibronectin and serves as an economical, xeno‐free, biodegradable, and functionally adaptable cell substrate. The ZT Fn substrate supports with high performance the propagation and long‐term self‐renewal of human embryonic stem cells while preserving their pluripotency. The ZT Fn polymer can, therefore, be proposed as an efficient and affordable replacement for fibronectin in clinical grade cell culturing. Further, it can be postulated that the ZT polymer has significant engineering potential for further orthogonal functionalization in complex cell applications.
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ZTFn supports pluripotency maintenance and neural crest differentiation.
“Similarly, ZTFn, a human protein based recombinant polymer modified with fibronectin domains, supports pluripotency maintenance and neural crest differentiation (Hill et al., 2019; Nesterenko et al., 2019; Nesterenko et al., 2020).”
From Challenges and solutions in transitioning to animal-free standards: a comprehensive analysis of components in human cell-based developmental neurotoxicity assays (2026) · cites this paper as Hill et al., 2019
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Spänle, J. V., Haiber, L. M., & Seeger, B. (2026) · Frontiers in Toxicology · doi:10.3389/ftox.2026.1800157 · Cited by 1 · see citing works
- Authors
- Hill, C. J., Fleming, J. R., Mousavinejad, M., Nicholson, R., Tzokov, S. B., Bullough, P. A., Bogomolovas, J., Morgan, M. R., Mayans, O., & Murray, P.
- Affiliations
- Department of Cellular and Molecular Physiology Institute of Translational Medicine University of Liverpool Nuffield Building, Crown Street Liverpool L69 3BX UK
- Department of Biology University of Konstanz 78457 Konstanz Germany
- Department of Molecular Biology and Biotechnology The Krebs Institute University of Sheffield Sheffield S10 2TN UK
- Department of Medicine UCSD La Jolla CA 92093 USA
- Department of Biochemistry Institute of Integrative Biology University of Liverpool Crown Street Liverpool L69 7ZB UK
- ORCID
- Murray, Patricia
- Venue
- Advanced Materials
- Publisher
- Wiley
- Published
- 2019-03-13
- Volume
- 31
- Issue
- 17
- ISSN
- 0935-9648
- 1521-4095
- Cited by
- 9
- References
- 2
- Language
- en
- Licence
- Funders
- Biotechnology and Biological Sciences Research Council (BB/I01666X/1)
- Wellcome Trust (204401/z/16/z)
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