Melis Isik
Bioactive and chemically defined hydrogels with tunable stiffness guide cerebral organoid formation and modulate multi-omics plasticity in cerebral organoids
Isik, Melis; Okesola, Babatunde O.; Eylem, Cemil Can; Kocak, Engin; Nemutlu, Emirhan; D'Este, Matteo; Mata, Alvaro; Derkus, Burak
Authors
BABATUNDE OKESOLA Babatunde.Okesola@nottingham.ac.uk
Nottingham Research Fellow
Cemil Can Eylem
Engin Kocak
Emirhan Nemutlu
Matteo D'Este
Professor ALVARO MATA A.Mata@nottingham.ac.uk
Chair in Biomedical Engineering & Materials
Burak Derkus
Abstract
Organoids are an emerging technology with great potential in human disease modelling, drug development, diagnosis, tissue engineering, and regenerative medicine. Organoids as 3D-tissue culture systems have gained special attention in the past decades due to their ability to faithfully recapitulate the complexity of organ-specific tissues. Despite considerable successes in culturing physiologically relevant organoids, their real-life applications are currently limited by challenges such as scarcity of an appropriate biomimetic matrix. Peptide amphiphiles (PAs) due to their well-defined chemistry, tunable bioactivity, and extracellular matrix (ECM)-like nanofibrous architecture represent an attractive material scaffold for organoids development. Using cerebral organoids (COs) as exemplar, we demonstrate the possibility to create bio-instructive hydrogels with tunable stiffness ranging from 0.69 kPa to 2.24 kPa to culture and induce COs growth. We used orthogonal chemistry involving oxidative coupling and supramolecular interactions to create two-component hydrogels integrating the bio-instructive activity and ECM-like nanofibrous architecture of a laminin-mimetic PAs (IKVAV-PA) and tunable crosslinking density of hyaluronic acid functionalized with tyramine (HA-Try). Multi-omics technology including transcriptomics, proteomics, and metabolomics reveals the induction and growth of COs in soft HA-Tyr hydrogels containing PA-IKVAV such that the COs display morphology and biomolecular signatures similar to those grown in Matrigel scaffolds. Our materials hold great promise as a safe synthetic ECM for COs induction and growth. Our approach represents a well-defined alternative to animal-derived matrices for the culture of COs and might expand the applicability of organoids in basic and clinical research. Statement of significance: Synthetic bio-instructive materials which display tissue-specific functionality and nanoscale architecture of the native extracellular matrix are attractive matrices for organoids development. These synthetic matrices are chemically defined and animal-free compared to current gold standard matrices such as Matrigel. Here, we developed hydrogel matrices with tunable stiffness, which incorporate laminin-mimetic peptide amphiphiles to grow and expand cerebral organoids. Using multi-omics tools, the present study provides exciting data on the effects of neuro-inductive cues on the biomolecular profiles of brain organoids.
Citation
Isik, M., Okesola, B. O., Eylem, C. C., Kocak, E., Nemutlu, E., D'Este, M., …Derkus, B. (2023). Bioactive and chemically defined hydrogels with tunable stiffness guide cerebral organoid formation and modulate multi-omics plasticity in cerebral organoids. Acta Biomaterialia, 171, 223-238. https://doi.org/10.1016/j.actbio.2023.09.040
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 25, 2023 |
Online Publication Date | Oct 23, 2023 |
Publication Date | 2023-11 |
Deposit Date | Oct 28, 2023 |
Publicly Available Date | Oct 24, 2024 |
Journal | Acta Biomaterialia |
Electronic ISSN | 1878-7568 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 171 |
Pages | 223-238 |
DOI | https://doi.org/10.1016/j.actbio.2023.09.040 |
Keywords | Peptide amphiphiles; hyaluronic acid; hydrogel; mechanotransduction; cerebral organoid; omics |
Public URL | https://nottingham-repository.worktribe.com/output/25683494 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S1742706123005883?via%3Dihub |
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Publisher Licence URL
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