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Engineered extracellular matrices facilitate brain organoids from human pluripotent stem cells.
Muñiz, Ayse J; Topal, Tugba; Brooks, Michael D; Sze, Angela; Kim, Do Hoon; Jordahl, Jacob; Nguyen, Joe; Krebsbach, Paul H; Savelieff, Masha G; Feldman, Eva L; Lahann, Joerg.
Afiliação
  • Muñiz AJ; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Topal T; Macromolecular Science and Engineering Program, University of Michigan, Ann Arbor, Michigan, USA.
  • Brooks MD; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Sze A; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Kim DH; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Jordahl J; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Nguyen J; Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
  • Krebsbach PH; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Savelieff MG; Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
  • Feldman EL; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
  • Lahann J; Biointerfaces Institute, University of Michigan, Ann Arbor, Michigan, USA.
Ann Clin Transl Neurol ; 10(7): 1239-1253, 2023 07.
Article em En | MEDLINE | ID: mdl-37283238
ABSTRACT

OBJECTIVE:

Brain organoids are miniaturized in vitro brain models generated from pluripotent stem cells, which resemble full-sized brain more closely than conventional two-dimensional cell cultures. Although brain organoids mimic the human brain's cell-to-cell network interactions, they generally fail to faithfully recapitulate cell-to-matrix interactions. Here, an engineered framework, called an engineered extracellular matrix (EECM), was developed to provide support and cell-to-matrix interactions to developing brain organoids.

METHODS:

We generated brain organoids using EECMs comprised of human fibrillar fibronectin supported by a highly porous polymer scaffold. The resultant brain organoids were characterized by immunofluorescence microscopy, transcriptomics, and proteomics of the cerebrospinal fluid (CSF) compartment.

RESULTS:

The interstitial matrix-mimicking EECM enhanced neurogenesis, glial maturation, and neuronal diversity from human embryonic stem cells versus conventional protein matrix (Matrigel). Additionally, EECMs supported long-term culture, which promoted large-volume organoids containing over 250 µL of CSF. Proteomics analysis of the CSF found it superseded previous brain organoids in protein diversity, as indicated by 280 proteins spanning 500 gene ontology pathways shared with adult CSF.

INTERPRETATION:

Engineered EECM matrices represent a major advancement in neural engineering as they have the potential to significantly enhance the structural, cellular, and functional diversity that can be achieved in advanced brain models.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Células-Tronco Pluripotentes Idioma: En Ano de publicação: 2023 Tipo de documento: Article