Abstract
Human brain experimental models recapitulating age- and disease-related characteristics are lacking. There is urgent need for human-specific tools that model the complex molecular and cellular interplay between different cell types to assess underlying disease mechanisms and test therapies. Here we present an adapted ex vivo organotypic slice culture method using human post-mortem brain tissue cultured at an air-liquid interface to also study brain white matter. We assessed whether these human post-mortem brain slices recapitulate the in vivo neuropathology and if they are suitable for pathophysiological, experimental and pre-clinical treatment development purposes, specifically regarding leukodystrophies. Human post-mortem brain tissue and cerebrospinal fluid were obtained from control, psychiatric and leukodystrophy donors. Slices were cultured up to six weeks, in culture medium with or without human cerebrospinal fluid. Human post-mortem organotypic brain slice cultures remained viable for at least six weeks ex vivo and maintained tissue structure and diversity of (neural) cell types. Supplementation with cerebrospinal fluid could improve slice recovery. Patient-derived organotypic slice cultures recapitulated and maintained known in vivo neuropathology. The cultures also showed physiologic multicellular responses to lysolecithin-induced demyelination ex vivo, indicating their suitability to study intrinsic repair mechanisms upon injury. The slice cultures were applicable for various experimental studies, as multi-electrode neuronal recordings. Finally, the cultures showed successful cell-type dependent transduction with gene therapy vectors. These human post-mortem organotypic brain slice cultures represent an adapted ex vivo model suitable for multifaceted studies of brain disease mechanisms, boosting translation from human ex vivo to in vivo. This model also allows for assessing potential treatment options, including gene therapy applications. Human post-mortem brain slice cultures are thus a valuable tool in preclinical research to study the pathomechanisms of a wide variety of brain diseases in living human tissue.
| Original language | English |
|---|---|
| Article number | 83 |
| Pages (from-to) | 1-17 |
| Number of pages | 17 |
| Journal | Acta Neuropathologica Communications |
| Volume | 12 |
| Early online date | 31 May 2024 |
| DOIs | |
| Publication status | Published - 2024 |
Bibliographical note
Publisher Copyright:© The Author(s) 2024.
Funding
The authors are grateful to the donors and their families, the autopsy team (Netherlands Brain Bank, The Netherlands) for their services and the Mortuary staff (Amsterdam UMC, The Netherlands) for their skillful assistance during the autopsies. We thank Leoni Hoogterp and Gemma van Leeuwen (Amsterdam UMC, The Netherlands) for assistance with maintaining the slice cultures and Anastasia Bomhof (Amsterdam UMC, The Netherlands) for technical assistance. We thank Gerald Schwank (University of Zurich, Switzerland) for providing the AAV-PHP.eB vector prep. We thank Tim Heistek (VU University, The Netherlands) for performing whole-cell patch-clamp recordings. We are grateful to Nanne Paauw (Amsterdam UMC, The Netherlands) for assistance with imaging on the Nikon LIPSI microscope. We are also grateful to Sowmya Sekizar and Anna Williams (University of Edinburgh, United Kingdom) for teaching BCP their method to culture organotypic mouse brain slices, on which the method described in this study is based. Author MBu is grateful to the late W.E. deMyer for the functional anatomy knowledge, on which the dissection strategy is based. NIW, MSvdK and MBu are members of the European Reference Network for Rare Neurological Disorders (ERN-RND), project ID 739510. This study was supported by a grant from ZonMw (TOP 91217006) and a grant from the VWM Families Foundation. Authors AL and NRCM received funding from the National MS society (Progressive MS alliance award, PA2021-36033) and AL and GMG from the Dutch National MS Foundation (OZ2021-008).
| Funders | Funder number |
|---|---|
| Gerald Schwank | |
| VWM Families Foundation | |
| University of Edinburgh | |
| Leoni Hoogterp and Gemma van Leeuwen | |
| Dr Tim Heistek | |
| Universität Zürich | |
| Vrije Universiteit Amsterdam | |
| NRCM | |
| Anastasia Bomhof | |
| Nederlandse Hersenbank | |
| ZONMW | TOP 91217006 |
| ZONMW | |
| National Multiple Sclerosis Society | PA2021-36033 |
| National Multiple Sclerosis Society | |
| Dutch national research foundation NWO-WOTRO, Science for Development | OZ2021-008 |
| ERN-RND | 739510 |
Keywords
- Gene therapy
- Human post-mortem brain
- Leukodystrophy
- Organotypic brain slice culture
- White matter
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