Evidence map›Paper›PMID 41410764›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Merkel cell mechanotransduction facilitates adult neurogenesis and cognition in an enriched environment.

Xing Luo, Qiang Liu, Dezhe Qin, Min Wang, Weixiang Guo

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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

5 authors.

Xing Luo *Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0009-0001-1465-3796
Qiang Liu *Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Dezhe QinInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Min WangInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Weixiang GuoInstitute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.ORCID 0000-0001-9303-6595

Funding

MOST | National Key Research and Development Program of China (NKPs) 2021ZD0202302MOST | National Natural Science Foundation of China (NSFC) 82271202 and 32394030
6 · The paper itself

Abstract

The tactile system empowers us to act on and interact with the changes of the external environment. In rodents, tactile sensation, a fundamental sense, is largely mediated via the vibrissae and the barrel cortex. However, it remains unclear how tactile perception reshape the brain when exploring a novel environment. Here, we showed that exposure to an enriched environment (EE) failed to enhance adult neurogenesis and cognition in the mice with defective touch perception due to loss of a mechanotransduction channel Piezo2 in Merkel cells. Moreover, we found an EE-activated neuraxis, in which the dentate gyrus received tactile input through a circuit that originated from the somatosensory cortex (S1) and relayed via dopaminergic neurons of the substantia nigra pars compacta (SNc). Defective touch perception diminished the S1 to SNc afferent, thereby reducing dopamine release. Notably, stimulation of the S1 to SNc afferent restored EE-induced adult neurogenesis and cognition in the mice with defective touch perception. Therefore, our study highlighted the important role of intact tactile processing in brain function.

Indexed as

CognitionMechanotransduction, CellularMerkel CellsNeurogenesisAnimalsDentate GyrusDopaminergic NeuronsEnvironmentIon ChannelsMaleMiceMice, Inbred C57BLSomatosensory CortexTouchTouch PerceptionIon ChannelsPiezo2 protein, mouseadult neurogenesisdopamineenriched environmentmechanotransductionPiezo2

Identifiers

PMID41410764
PMCPMC12745700

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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.