Evidence map›Paper›PMID 39299992›Full record

ArticleJournal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology2025

Tanycytes from a bird's eye view: gene expression profiling of the tanycytic region under different seasonal states in the Svalbard ptarmigan.

Daniel Appenroth, Alexander C West, Shona H Wood, David G Hazlerigg

Abstract read
In one paragraph

Article in Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Daniel AppenrothArctic Seasonal Timekeeping Initiative (ASTI), Arctic Chronobiology & Physiology, Arctic & Marine Biology, BFE, UiT - Arctic University of Norway, Tromsø, Norway. daniel.appenroth@uit.no.ORCID http://orcid.org/0000-0003-0197-3739
Alexander C WestArctic Seasonal Timekeeping Initiative (ASTI), Arctic Chronobiology & Physiology, Arctic & Marine Biology, BFE, UiT - Arctic University of Norway, Tromsø, Norway.ORCID http://orcid.org/0000-0003-3934-5068
Shona H WoodArctic Seasonal Timekeeping Initiative (ASTI), Arctic Chronobiology & Physiology, Arctic & Marine Biology, BFE, UiT - Arctic University of Norway, Tromsø, Norway.ORCID http://orcid.org/0000-0002-8273-4045
David G HazleriggArctic Seasonal Timekeeping Initiative (ASTI), Arctic Chronobiology & Physiology, Arctic & Marine Biology, BFE, UiT - Arctic University of Norway, Tromsø, Norway.ORCID http://orcid.org/0000-0003-4884-8409

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In mammals and birds, tanycytes are known to regulate thyroid hormone conversion, and this process is central to the control of seasonal reproduction. In mammals, this cell type is also implicated in retinoic acid signalling, neurogenesis, and nutritional gatekeeping, all of which have been linked to hypothalamic regulation of energy metabolism. Less is known about these potential wider roles of tanycytes in birds. To address this gap, we combined LASER capture microdissection and transcriptomics to profile the tanycytic region in male Svalbard ptarmigan, a High Arctic species with photoperiod-dependent seasonal rhythms in reproductive activation and body mass. Short photoperiod (SP) adapted birds were transferred to constant light (LL) to trigger breeding and body mass loss. After five months under LL, the development of photorefractoriness led to spontaneous re-emergence of the winter phenotype, marked by the termination of breeding and gain in body mass. The transfer from SP to LL initiated gene expression changes in both thyroid hormone and retinoic acid pathways, as described in seasonal mammals. Furthermore, transcriptomic signatures of cell differentiation and migration were observed. Comparison to data from Siberian hamsters demonstrated that a photoperiod-dependent re-organisation of the hypothalamic tanycytic region is likely a conserved feature. Conversely, the spontaneous development of photorefractoriness showed a surprisingly small number of genes that reverted in expression level, despite reversal of the reproductive and metabolic phenotype. Our data suggest general conservation of tanycyte biology between photoperiodic birds and mammals and raise questions about the mechanistic origins of the photorefractory state.

Indexed as

Ependymoglial CellsGalliformesSeasonsAnimalsGene Expression ProfilingMalePhotoperiodReproductionTranscriptomeBirdsMetabolismPhotoperiodSeasonalTanycytes

Identifiers

PMID39299992
PMCPMC11846777

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.