Evidence map›Paper›PMID 41329355›Full record

ArticleCellular and molecular life sciences : CMLS2025

Epididymal epithelial cells facilitate NEU1 loading to modulate sperm α-2,6 sialylation, enhance maturation and motility.

Shiqi Yi, Ruohan Wang, Yingchun Hu, Shukai Wang, Linyu Zhang, Xinrui Sun, Xin Yuan, Jiajie Li, Shuangling Zou, Hongxiang Wang and 1 more

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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.

Shiqi YiCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Ruohan WangCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Yingchun HuCollege of Life Sciences, Peking University, Beijing, 100871, China.
Shukai WangDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Linyu ZhangCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Xinrui SunCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Xin YuanCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Jiajie LiDepartment of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, China.
Shuangling ZouCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China.
Hongxiang WangDepartment of Urology and Andrology, School of Medicine, Renji Hospital, Shanghai Jiao Tong University, Shanghai, 200127, China.
Fang MaCenter for Translational Medicine, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), West China Second University Hospital, Ministry of Education, Sichuan University, Chengdu, 610041, Sichuan, China. mafangmed@scu.edu.cn.ORCID http://orcid.org/0000-0002-7781-821X

Funding

National Natural Science Foundation of China 31470797Sichuan Provincial Administration of Traditional Chinese Medicine 2023MS036
6 · The paper itself

Abstract

backgroundMale infertility is a prevalent reproductive disorder worldwide, with decreased sperm quality-particularly reduced motility and fertilization capacity-being one of its common causes. Sperm maturation is a complex process involving multiple molecular mechanisms, the specific pathways regulating sperm motility remain unclear and require further investigation. Among these mechanisms, sialylation serves as an important glycosylation modification during sperm maturation and capacitation, playing a crucial role in these processes. Nonetheless, the specific function of Neuraminidase-1 (NEU1), a kind of sialidase, in sperm maturation and function remains poorly understood. This study aims to investigate the origin and function of NEU1 in sperm, as well as its impact on sperm motility and fertilization potential, providing new insights into its role in male infertility.

methodsA combination of computational prediction and experimental validation was used to assess the expression profile of sialylation-related enzymes in the male reproductive tract, identifying NEU1 as a candidate for further investigation. Immunofluorescence, Western blotting, and flow cytometry were performed to analyze the expression pattern of NEU1 in human and murine sperm. Functional studies were conducted by inhibiting NEU1 activity to examine its effects on sperm motility and fertilization capacity. Additionally, NEU1 expression was compared between asthenozoospermic and normozoospermic individuals, and in vitro fertilization (IVF) assays were performed to evaluate its role in fertilization. Furthermore, a murine model was used to explore the origin of NEU1 during sperm maturation, particularly focusing on whether it is secreted and transferred onto sperm by epididymal epithelial cells.

resultsThis study demonstrated that NEU1 is highly expressed in both human and murine sperm, and its expression level is closely associated with sperm motility and fertilization capacity. Sperm with higher motility exhibited significantly elevated NEU1 expression, which positively correlated with sperm kinematic parameters such as velocity and linearity. Inhibition of NEU1 activity resulted in a marked decline in sperm motility and fertilization potential. Furthermore, NEU1 is secreted by epididymal epithelial cells and subsequently transferred to the sperm surface. It regulates α-2,6 sialylation, thereby influencing sperm maturation, energy metabolism, and capacitation. IVF assays further confirmed a significant correlation between NEU1 expression and fertilization success.

conclusionThis study identifies NEU1 as a key regulatory enzyme on the sperm surface, directly influencing sperm motility and fertilization capacity. NEU1 is secreted by epididymal epithelial cells and transferred onto sperm, mediating sialylation modifications and regulating sperm capacitation and metabolic processes. These findings provide novel insights into the functional role of sialidases in sperm maturation and function, offering potential biomarkers and therapeutic targets for the diagnosis and treatment of male infertility.

Indexed as

EpididymisEpithelial CellsN-Acetylneuraminic AcidNeuraminidaseSpermatozoaSperm MaturationSperm MotilityAnimalsHumansInfertility, MaleMaleMiceMice, Inbred C57BLSperm CapacitationN-Acetylneuraminic AcidNEU1 protein, humanNeu1 protein, mouseNeuraminidaseEpididymal epitheliumMale infertilityNeuraminidase-1SialylationSperm maturationSperm motility

Identifiers

PMID41329355
PMCPMC12672989

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.