Evidence map›Paper›PMID 40301264›Full record

ReviewAdvances in experimental medicine and biology2025

Interacting Fat1 and Dchs Planar Cell Polarity Proteins Supported by Fjx1 Serve as Heterodimeric Intercellular Bridges Crucial to Support Spermatogenesis.

Tiao Bu, Lingling Wang, Xiaolong Wu, Sheng Gao, Damin Yun, Baiping Mao, Linxi Li, Fei Sun, C Yan Cheng

Abstract readReview
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In one paragraph

Review in Advances in experimental medicine and biology, 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

9 authors.

Tiao BuDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Lingling WangDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Xiaolong WuDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Sheng GaoDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Damin YunDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Baiping MaoThe Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Linxi LiThe Second Affiliated Hospital and Yuying Children's Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Fei SunDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China. sunfeisrrsh@zju.edu.cn.
C Yan ChengDepartment of Urology and Andrology, Sir Run-run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China. L211064@zju.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies of the planar cell polarity (PCP) protein complexes Fat1/Fjx1 and Dchs/Fjx1 that form heterotypic interacting bridges of Fat1-Dchs between adjacent cells to confer PCP, as noted in Drosophila, are also found in mammalian cells and tissues as orthologs, such as in Sertoli cells and condensed spermatids in the seminiferous epithelium of the testis. Recent studies have shown that these two interacting PCP protein complexes are also crucial regulators of microtubule and actin dynamics, modulating the polymerization of both microtubules and actin filaments in the testis. In this review, we provide a brief update and thought-provoking concept on the PCP core proteins and the associated downstream signaling pathways utilized by PCP proteins to confer PCP and regulation of the microtubule and actin cytoskeletons in the testis. However, we focus on recent data in the field on the Fat1/Fjx1 and Dchs/Fjx1 protein complexes, which are also heterotypic interacting protein complexes, and their functional role in modulating the microtubule and actin cytoskeletal organization. Based on these recent findings, we formulate a hypothetic model depicting the role of these two PCP protein complexes in modulating the timely "opening" and "closing" of the blood-testis barrier (BTB) formed by adjacent Sertoli cells near the base of the seminiferous epithelium. Additionally, these two PCP protein complexes also modulate cytoskeletal dynamics between Sertoli cells and condensed spermatids to support haploid spermatid transport across the seminiferous epithelium during their structural transformation through spermiogenesis, and their eventual release at spermiation during the epithelial cycle of spermatogenesis. This hypothetical model will provide a useful framework for designing functional experiments to understand the role of PCP proteins in supporting spermatogenesis.

Indexed as

Cell PolaritySpermatogenesisAnimalsHumansMaleMicrotubulesSertoli CellsSignal TransductionDchsElongated spermatidsFatFat1Fjx1Planar cell polaritySertoli cellsSpermatogenesis

Identifiers

What Socratic holds

Textmetadata
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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 Socratic graph.