Evidence map›Paper›PMID 40109271›Full record

ArticleMolecular ecology resources2025

Cochlear Cell Atlas of Two Laryngeal Echolocating Bats-New Evidence for the Adaptive Nervous Physiology in Constant Frequency Bat.

Xue Wang, Mingyue Bao, Hui Wang, Ruyi Sun, Wentao Dai, Keping Sun, Yue Zhu, Yingting Pu, Yujia Chu, Xintong Li and 5 more

Abstract read
In one paragraph

Article in Molecular ecology resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Xue WangCollege of Life Science, Jilin Agricultural University, Changchun, China.ORCID https://orcid.org/0000-0001-5195-3969
Mingyue BaoCollege of Life Science, Jilin Agricultural University, Changchun, China.
Hui WangCollege of Life Science, Jilin Agricultural University, Changchun, China.
Ruyi SunCollege of Life Science, Jilin Agricultural University, Changchun, China.
Wentao DaiJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.
Keping SunJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.ORCID https://orcid.org/0000-0002-4227-9818
Yue ZhuJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.
Yingting PuJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.
Yujia ChuCollege of Life Science, Jilin Agricultural University, Changchun, China.ORCID https://orcid.org/0000-0002-6526-3835
Xintong LiCollege of Life Science, Jilin Agricultural University, Changchun, China.
Tianhui WangCollege of Life Science, Jilin Agricultural University, Changchun, China.
Minjie ZhangCollege of Life Science, Jilin Agricultural University, Changchun, China.
Aiqing LinJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.ORCID https://orcid.org/0000-0002-2832-2605
Jiqian LiJilin Provincial Key Laboratory of Animal Resource Conservation and Utilization, Northeast Normal University, Changchun, China.
Jiang FengCollege of Life Science, Jilin Agricultural University, Changchun, China.

Funding

National Natural Science Foundation of China 32001089National Natural Science Foundation of China 32371561Natural Science Foundation of Jilin Province 20240101225JC
6 · The paper itself

Abstract

Bats have evolved highly adapted auditory mechanisms associated with ecological specialisation. However, there is scattered knowledge about the neurophysiological and cellular basis underlying high-frequency hearing in echolocating bats. Herein, the total cochlear cell atlas of Rhinolophus ferrumequinum (constant frequency (CF) bat) and Myotis pilosus (frequency modulated (FM) bat) was conducted using the 10x Genomics single-nucleus RNA sequencing method. Differences in the proportion of cochlear cell types, especially for the neural cells, were detected between these two bat species. Previously, genes upregulated in the cochlea of CF compared with FM bats, were found to be mostly related to nervous activities. After mapping to the cochlear cell atlas, we found that the upregulated genes were from neural cells, lateral wall cells and neurosensory epithelium cells. A class of specific neurons and associated functions was detected in the cochlea of R. ferrumequinum, revealed by cross-species single-cell transcriptomic analyses. Furthermore, molecular evidence for the differentiation from glial cells to neuronal cells was also uncovered in the cochlea of R. ferrumequinum. Overall, this study identified specific cellular molecular properties that constitute the neuroanatomical evolutionary dynamics underlying distinct echolocating types of bats and provided new molecular evidence for high-frequency hearing of echolocating bats, promoting related studies about ecological adaptation and evolution.

Indexed as

Adaptation, PhysiologicalChiropteraCochleaEcholocationAnimalsGene Expression ProfilingNeuronsTranscriptomebatscell atlascochleaneuronssnRNA‐seq

Identifiers

PMID40109271
PMCPMC12225709

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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.