HIF1α-dependent induction of the T-Type calcium channel CaV3.2 mediates hypoxia-induced neuronal hyperexcitability Article Swipe
Anna R. Tröscher
,
Despina Tsortouktzidis
,
Franziska Ammer-Pickhardt
,
Martin Aichholzer
,
Philip-Rudolf Rauch
,
Tobias Rossmann
,
Nico Stroh-Holly
,
Baran Alti
,
Andreas Gruber
,
Raimund Helbok
,
Jan Haubold
,
Christian Thome
,
Maren Engelhardt
,
Tim J. von Oertzen
,
Susanne Schoch
,
Albert J. Becker
,
Karen M. J. van Loo
·
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1101/2025.10.13.682038
YOU?
·
· 2025
· Open Access
·
· DOI: https://doi.org/10.1101/2025.10.13.682038
Post-stroke epilepsy (PSE) is a leading cause of acquired epilepsy in adults, yet the molecular mechanisms linking post-ischemic hypoxia to neuronal hyperexcitability remain poorly understood. The transcription factor hypoxia-inducible factor 1α (HIF1α) is a central mediator of the cellular response to hypoxia and may contribute to epileptogenesis by regulating ion channel expression. Here, we identify the T-type calcium channel CaV3.2 (encoded by Cacna1h ) as a direct transcriptional target of HIF1α and demonstrate its role in hypoxia-induced network hyperexcitability. Oxygen-glucose deprivation followed by reoxygenation (OGD/R) induced a persistent increase in neuronal firing rate. In murine and human organotypic brain slices, hypoxia led to a marked increase in HIF1α and Cacna1h expression at both transcript and protein levels. Using neuronal cell lines and primary cortical neurons we show that HIF1α activation through HIF1α overexpression, consistently increases Cacna1h expression. In NS20Y cells, overexpression of a normoxia-stable HIF1α variant increased Cacna1h promoter activity in both fluorescent and dual-luciferase reporter assays. The same effect was observed in primary cortical neurons, where HIF1α overexpression also elevated network activity measured by multielectrode array recordings, replicating the effect of the OGD/R model. Together, these results establish HIF1α as a key transcriptional regulator of CaV3.2 in neurons and reveal a conserved hypoxia-HIF1α-CaV3.2 pathway that enhances neuronal excitability. This mechanism may underlie hypoxia-induced network hyperactivity and contribute to the pathogenesis of post-ischemic epileptogenesis, offering a potential molecular target for intervention.
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- Type
- preprint
- Language
- en
- Landing Page
- https://doi.org/10.1101/2025.10.13.682038
- https://www.biorxiv.org/content/biorxiv/early/2025/10/14/2025.10.13.682038.full.pdf
- OA Status
- green
- References
- 24
- OpenAlex ID
- https://openalex.org/W4415163368
All OpenAlex metadata
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- OpenAlex ID
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https://openalex.org/W4415163368Canonical identifier for this work in OpenAlex
- DOI
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https://doi.org/10.1101/2025.10.13.682038Digital Object Identifier
- Title
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HIF1α-dependent induction of the T-Type calcium channel CaV3.2 mediates hypoxia-induced neuronal hyperexcitabilityWork title
- Type
-
preprintOpenAlex work type
- Language
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enPrimary language
- Publication year
-
2025Year of publication
- Publication date
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2025-10-14Full publication date if available
- Authors
-
Anna R. Tröscher, Despina Tsortouktzidis, Franziska Ammer-Pickhardt, Martin Aichholzer, Philip-Rudolf Rauch, Tobias Rossmann, Nico Stroh-Holly, Baran Alti, Andreas Gruber, Raimund Helbok, Jan Haubold, Christian Thome, Maren Engelhardt, Tim J. von Oertzen, Susanne Schoch, Albert J. Becker, Karen M. J. van LooList of authors in order
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https://doi.org/10.1101/2025.10.13.682038Publisher landing page
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https://www.biorxiv.org/content/biorxiv/early/2025/10/14/2025.10.13.682038.full.pdfDirect link to full text PDF
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YesWhether a free full text is available
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-
greenOpen access status per OpenAlex
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https://www.biorxiv.org/content/biorxiv/early/2025/10/14/2025.10.13.682038.full.pdfDirect OA link when available
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| abstract_inverted_index.expression | 111 |
| abstract_inverted_index.mechanisms | 16 |
| abstract_inverted_index.persistent | 88 |
| abstract_inverted_index.regulating | 49 |
| abstract_inverted_index.transcript | 114 |
| abstract_inverted_index.Post-stroke | 1 |
| abstract_inverted_index.demonstrate | 73 |
| abstract_inverted_index.deprivation | 81 |
| abstract_inverted_index.expression. | 52, 137 |
| abstract_inverted_index.fluorescent | 153 |
| abstract_inverted_index.organotypic | 98 |
| abstract_inverted_index.recordings, | 178 |
| abstract_inverted_index.replicating | 179 |
| abstract_inverted_index.understood. | 25 |
| abstract_inverted_index.consistently | 134 |
| abstract_inverted_index.pathogenesis | 221 |
| abstract_inverted_index.excitability. | 209 |
| abstract_inverted_index.hyperactivity | 216 |
| abstract_inverted_index.intervention. | 231 |
| abstract_inverted_index.post-ischemic | 18, 223 |
| abstract_inverted_index.reoxygenation | 84 |
| abstract_inverted_index.transcription | 27 |
| abstract_inverted_index.Oxygen-glucose | 80 |
| abstract_inverted_index.multielectrode | 176 |
| abstract_inverted_index.overexpression | 141, 169 |
| abstract_inverted_index.dual-luciferase | 155 |
| abstract_inverted_index.epileptogenesis | 47 |
| abstract_inverted_index.hypoxia-induced | 77, 214 |
| abstract_inverted_index.normoxia-stable | 144 |
| abstract_inverted_index.overexpression, | 133 |
| abstract_inverted_index.transcriptional | 68, 194 |
| abstract_inverted_index.epileptogenesis, | 224 |
| abstract_inverted_index.hyperexcitability | 22 |
| abstract_inverted_index.hypoxia-inducible | 29 |
| abstract_inverted_index.hyperexcitability. | 79 |
| abstract_inverted_index.hypoxia-HIF1α-CaV3.2 | 204 |
| cited_by_percentile_year | |
| countries_distinct_count | 0 |
| institutions_distinct_count | 17 |
| citation_normalized_percentile.value | 0.54614695 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |