Evidence map›Paper›PMID 37694824›Full record

ArticleBiology of reproduction2023

Segmental differentiation of the murine epididymis: identification of segment-specific, GM1-enriched vesicles and regulation by luminal fluid factors†.

Danielle M Sosnicki, Roy Cohen, Atsushi Asano, Jacquelyn L Nelson, Chinatsu Mukai, Pierre Comizzoli, Alexander J Travis

Open access · bronzeAbstract read
In one paragraph

Article in Biology of reproduction, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Metabolomic Analysis of Cauda Epididymal Fluid in Yaks and Cattle.Animals : an open access journal from MDPI · 2025
    Article
  2. Frontiers in veterinary science · 2025
    Article
  3. Article
  4. 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

7 authors at 3 institutions in 2 countries.

Danielle M SosnickiCornell University, Baker Institute for Animal Health, Ithaca, NY, USA.
Roy CohenCornell University, Baker Institute for Animal Health, Ithaca, NY, USA.
Atsushi AsanoUniversity of Tsukuba, Faculty of Life and Environmental Sciences, Tsukuba, Japan.
Jacquelyn L NelsonCornell University, Baker Institute for Animal Health, Ithaca, NY, USA.
Chinatsu MukaiCornell University, Baker Institute for Animal Health, Ithaca, NY, USA.
Pierre ComizzoliSmithsonian's National Zoo and Conservation Biology Institute, Department of Reproductive Sciences, Washington, DC, USA.
Alexander J TravisCornell University, Baker Institute for Animal Health, Ithaca, NY, USA.
Cornell University · USSmithsonian Conservation Biology Institute · USUniversity of Tsukuba · JP

Funding

Membrane lipid regulation of calcium channels in sperm.R01HD093827 · NICHD · CORNELL UNIVERSITY · PI TRAVIS, ALEXANDER J · 2019 to 2023
$2.1M
NICHD NIH HHS R01 HD093827NIH HHS R01-HD093827
6 · The paper itself

Abstract

The murine epididymis has 10 distinct segments that provide the opportunity to identify compartmentalized cell physiological mechanisms underlying sperm maturation. However, despite the essential role of the epididymis in reproduction, remarkably little is known about segment-specific functions of this organ. Here, we investigate the dramatic segmental localization of the ganglioside GM1, a glycosphingolipid already known to play key roles in sperm capacitation and acrosome exocytosis. Frozen tissue sections of epididymides from adult mice were treated with the binding subunit of cholera toxin conjugated to AlexaFluor 488 to label GM1. We report that GM1-enriched vesicles were found exclusively in principal and clear cells of segment 2. These vesicles were also restricted to the lumen of segment 2 and did not appear to flow with the sperm into segment 3, within the limits of detection by confocal microscopy. Interestingly, this segment-specific presence was altered in several azoospermic mouse models and in wild-type mice after efferent duct ligation. These findings indicate that a lumicrine factor, itself dependent on spermatogenesis, controls this segmental differentiation. The RNA sequencing results confirmed global de-differentiation of the proximal epididymal segments in response to efferent duct ligation. Additionally, GM1 localization on the surface of the sperm head increased as sperm transit through segment 2 and have contact with the GM1-enriched vesicles. This is the first report of segment-specific vesicles and their role in enriching sperm with GM1, a glycosphingolipid known to be critical for sperm function, providing key insights into the segment-specific physiology and function of the epididymis.

Indexed as

EpididymisG(M1) GangliosideAnimalsMaleMiceSemenSpermatogenesisSpermatozoaG(M1) Gangliosideefferent duct ligationepididymisganglioside GM1lumicrine signalingmembrane raftsperm

Identifiers

PMID37694824
PMCPMC10724454
OpenAlexW4386592778

What OpenQuestion holds

Textmetadata
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.