Abstract
Regenerative medicine offers a promising approach to treat brain injuries, yet challenges persist in promoting neuronal survival and integration. Recent studies demonstrate that human cells implanted into rodent brains can exhibit plasticity, integrate into neural circuits and alleviate functional deficits. However, integration is often poor, with inadequate vascularization, and insufficient support cells such as astrocytes. Astrocytes play a crucial role in neuronal development and recovery by releasing growth factors, facilitating synaptogenesis, and promoting blood vessel formation. This study investigated human neuronal progenitor cells cultured alone or cultured with mouse astrocytes and formed into 3D constructs using microfluidics. Co-cultures exhibited enhanced neuronal maturation, viability, and density. Following implantation into mouse brains, co-cultures reduced lesion size, increased axonal growth, and improved astrocyte coupling to blood vessels within the graft. Additionally, we show that NPCs and co-cultures increased astrocyte size in implants. Deconvolved high-resolution microscopy identified synapses and optogenetics showed functional connections between the host and implants. These findings underscore the essential role of astrocytes in enhancing neuronal tissue integration and advancing brain injury treatments. [Abstract copyright: © 2026 The Author(s). Advanced Science published by Wiley‐VCH GmbH.]
| Original language | English |
|---|---|
| Article number | e07423 |
| Number of pages | 26 |
| Journal | Advanced science (Weinheim, Baden-Wurttemberg, Germany) |
| Volume | 13 |
| Issue number | 20 |
| Early online date | 26 Feb 2026 |
| DOIs | |
| Publication status | Published - 9 Apr 2026 |
Bibliographical note
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.© 2026 The Author(s). Advanced Science published by Wiley-VCH GmbH
Funding
| Funders | Funder number |
|---|---|
| National Institutes of Health | |
| John Fell Fund, University of Oxford | |
| British Heart Foundation | |
| U.S. Department of Health and Human Services | |
| University of Oxford | |
| Fundação de Amparo à Pesquisa do Estado de São Paulo | 2022/06554‐7 |
| UK Dementia Research Institute | UK DRI‐8203 |
| UK Research and Innovation | EP/Y023684/1 |
| Medical Research Council | MR/W027119/1 |
| BHF Centre of Research Excellence, Oxford | RE/24/130024 |
| European Research Council | ERC‐2022‐ADG‐101096882 |
| Biotechnology and Biological Sciences Research Council | BB/Y512874/1 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Traumatic brain injury
- Cerebral cortex development
- Microfluidics tissue printing
- Brain implantation
- Astrocytes
- Brain
- Neurons
- Humans
- Cells, Cultured
- Coculture Techniques/methods
- Brain Injuries/therapy
- Animals
- Astrocytes/physiology
- Mice
- Regenerative Medicine/methods
- Neural Stem Cells/cytology
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