Advancing next-generation brain organoid platforms for investigating traumatic brain injury from repeated blast exposures

dc.contributor.authorBar-Kochba, Eyal
dc.contributor.authorCarneal, Catherine M.
dc.contributor.authorAlphonse, Vanessa D.
dc.contributor.authorTimm, Andrea C.
dc.contributor.authorErnlund, Amanda W.
dc.contributor.authorRodriguez, Carissa L.
dc.contributor.authorMorales Pantoja, Itzy E.
dc.contributor.authorSmirnova, Lena
dc.contributor.authorHartung, Thomas
dc.contributor.authorMerkle, Andrew C.
dc.date.accessioned2025-09-10T08:29:09Z
dc.date.available2025-09-10T08:29:09Z
dc.date.issued2025-06-18
dc.description.abstractService members and law enforcement personnel are frequently exposed to blast overpressure during training and combat due to the use of heavy weaponry such as large-caliber rifles, explosives, and ordnance. The cumulative effects of these repeated low-level (<4 psi) blast exposures can lead to physical and cognitive deficits that are poorly understood. Brain organoids—human stem cell-derived three-dimensional in vitro culture systems that self-organize to recapitulate the in vivo environment of the human brain—are a promising alternative biological model to traditional cellular cultures and animal models, offering a unique opportunity for studying the mechanisms of mild blast-induced traumatic brain injury (mbTBI) resulting from repeated exposure. In this article, we review the current state of brain organoid models and discuss future directions for advancing their physiological relevance for studying mbTBI. These will be presented within a framework for developing next-generation platforms that integrate relevant loading devices, as well as non-invasive technologies for assessing the brain organoid’s response while increasing throughput. These next-generation platforms aim to accelerate the development of new interventions for mbTBI.
dc.description.versionpublisheddeu
dc.identifier.doi10.3389/fbioe.2025.1553609
dc.identifier.ppn1935534246
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/74514
dc.language.isoeng
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjecttraumatic brain injury
dc.subjectbrain organoids
dc.subjectrepeated blast
dc.subjectlow-level blast
dc.subjectprimary blast
dc.subjectin vitro model
dc.subject.ddc570
dc.titleAdvancing next-generation brain organoid platforms for investigating traumatic brain injury from repeated blast exposureseng
dc.typeJOURNAL_ARTICLE
dspace.entity.typePublication
kops.citation.bibtex
@article{BarKochba2025-06-18Advan-74514,
  title={Advancing next-generation brain organoid platforms for investigating traumatic brain injury from repeated blast exposures},
  year={2025},
  doi={10.3389/fbioe.2025.1553609},
  volume={13},
  journal={Frontiers in Bioengineering and Biotechnology},
  author={Bar-Kochba, Eyal and Carneal, Catherine M. and Alphonse, Vanessa D. and Timm, Andrea C. and Ernlund, Amanda W. and Rodriguez, Carissa L. and Morales Pantoja, Itzy E. and Smirnova, Lena and Hartung, Thomas and Merkle, Andrew C.},
  note={Article Number: 1553609}
}
kops.citation.iso690BAR-KOCHBA, Eyal, Catherine M. CARNEAL, Vanessa D. ALPHONSE, Andrea C. TIMM, Amanda W. ERNLUND, Carissa L. RODRIGUEZ, Itzy E. MORALES PANTOJA, Lena SMIRNOVA, Thomas HARTUNG, Andrew C. MERKLE, 2025. Advancing next-generation brain organoid platforms for investigating traumatic brain injury from repeated blast exposures. In: Frontiers in Bioengineering and Biotechnology. Frontiers. 2025, 13, 1553609. eISSN 2296-4185. Verfügbar unter: doi: 10.3389/fbioe.2025.1553609deu
kops.citation.iso690BAR-KOCHBA, Eyal, Catherine M. CARNEAL, Vanessa D. ALPHONSE, Andrea C. TIMM, Amanda W. ERNLUND, Carissa L. RODRIGUEZ, Itzy E. MORALES PANTOJA, Lena SMIRNOVA, Thomas HARTUNG, Andrew C. MERKLE, 2025. Advancing next-generation brain organoid platforms for investigating traumatic brain injury from repeated blast exposures. In: Frontiers in Bioengineering and Biotechnology. Frontiers. 2025, 13, 1553609. eISSN 2296-4185. Available under: doi: 10.3389/fbioe.2025.1553609eng
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