Extracellular matrix-templating fibrous hydrogels promote ovarian tissue remodeling and oocyte growth.

Biomimetic matrix Fibrous hydrogels Ovarian follicle

Journal

Bioactive materials
ISSN: 2452-199X
Titre abrégé: Bioact Mater
Pays: China
ID NLM: 101685294

Informations de publication

Date de publication:
Feb 2024
Historique:
received: 16 03 2023
revised: 14 08 2023
accepted: 01 10 2023
medline: 25 10 2023
pubmed: 25 10 2023
entrez: 25 10 2023
Statut: epublish

Résumé

Synthetic matrices which mimic the extracellular composition of native tissue create a comprehensive model for studying development and disease. Here, we have engineered a composite material which retains cell-secreted ECM for the culture of ovarian follicles by embedding electrospun dextran fibers functionalized with basement membrane binder (BMB) peptide in PEG hydrogels. In the presence of ECM-sequestering fibers, encapsulated immature primordial follicles and ovarian stromal cells aggregated into large organoid-like structures with dense deposition of laminin, perlecan, and collagen I, leading to steroidogenesis and significantly greater rates of oocyte survival and growth. We determined that cell aggregation restored key cell-cell interactions critical for oocyte survival, whereas oocyte growth was dependent on cell-matrix interactions achieved in the presence of BMB. Here we have shown that sequestration and retention of cell-secreted ECM along synthetic fibers mimics fibrous ECM structure and restores the cell-cell and cell-matrix interactions critical for engineering an artificial ovary.

Identifiants

pubmed: 37876554
doi: 10.1016/j.bioactmat.2023.10.001
pii: S2452-199X(23)00306-7
pmc: PMC10590725
doi:

Types de publication

Journal Article

Langues

eng

Pagination

292-303

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Claire E Nason-Tomaszewski (CE)

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

Emily E Thomas (EE)

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

Daniel L Matera (DL)

Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

Brendon M Baker (BM)

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.

Ariella Shikanov (A)

Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI 48109, USA.
Cellular and Molecular Biology Program, University of Michigan, Ann Arbor, MI 48109, USA.

Classifications MeSH