Evidence map›Paper›PMID 39773308›Full record

ArticleeLife2025

Atlas of Fshr expression from novel reporter mice.

Hongqian Chen, Hui-Qing Fang, Jin-Tao Liu, Shi-Yu Chang, Li-Ben Cheng, Ming-Xin Sun, Jian-Rui Feng, Ze-Min Liu, Yong-Hong Zhang, Clifford J Rosen and 1 more

Abstract read
In one paragraph

Article in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. One size does not fit all: how type of menopause and hormone therapy matters for brain health.The British journal of psychiatry : the journal of mental science · 2025
    Review
  6. Article
  7. Review
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

11 authors.

Hongqian Chen *Laboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Hui-Qing Fang *Laboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Jin-Tao LiuLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Shi-Yu ChangLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Li-Ben ChengLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Ming-Xin SunLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Jian-Rui FengLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Ze-Min LiuLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.ORCID https://orcid.org/0000-0003-4810-9200
Yong-Hong ZhangLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.
Clifford J RosenMaine Medical Center Research Institute, Scarborough, United States.ORCID https://orcid.org/0000-0003-3436-8199
Peng LiuLaboratory of Bone and Adipose Biology, Shanxi Medical University, Taiyuan, China.ORCID https://orcid.org/0000-0001-5607-2482

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The FSH-FSHR pathway has been considered an essential regulator in reproductive development and fertility. But there has been emerging evidence of FSHR expression in extragonadal organs. This poses new questions and long-term debates regarding the physiological role of the FSH-FSHR, and underscores the need for reliable, in vivo analysis of FSHR expression in animal models. However, conventional methods have proven insufficient for examining FSHR expression due to several limitations. To address this challenge, we developed Fshr-ZsGreen reporter mice under the control of Fshr endogenous promoter using CRISPR-Cas9. With this novel genetic tool, we provide a reliable readout of Fshr expression at single-cell resolution level in vivo and in real time. Reporter animals were also subjected to additional analyses,to define the accurate expression profile of FSHR in gonadal and extragonadal organs/tissues. Our compelling results not only demonstrated Fshr expression in intragonadal tissues but also, strikingly, unveiled notably increased expression in Leydig cells, osteoblast lineage cells, endothelial cells in vascular structures, and epithelial cells in bronchi of the lung and renal tubes. The genetic decoding of the widespread pattern of Fshr expression highlights its physiological relevance beyond reproduction and fertility, and opens new avenues for therapeutic options for age-related disorders of the bones, lungs, kidneys, and hearts, among other tissues. Exploiting the power of the Fshr knockin reporter animals, this report provides the first comprehensive genetic record of the spatial distribution of FSHR expression, correcting a long-term misconception about Fshr expression and offering prospects for extensive exploration of FSH-FSHR biology.

Indexed as

Genes, ReporterReceptors, FSHAnimalsCRISPR-Cas SystemsFemaleMaleMiceMice, TransgenicReceptors, FSHcell biologyFSHFSHRgene expressionGFPLeydig cellsmouseosteoblasts

Identifiers

PMID39773308
PMCPMC11709436

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.