Evidence map›Paper›PMID 41715063›Full record

ArticleBMC biology2026

Chloride Intracellular Channel 4 (CLIC4) controls volume regulation in sperm development via Protein Kinase C (PKC).

Veronica Loyo-Celis, Shridhar Sanghvi, Satish K Raut, Hiram Pacheco Castillo, Jose Luis de la Vega Beltran, Gerardo Orta, Alejandra Montanez-Barragan, Aaryan Patel, Victor Xavier Abonza Amaro, Shubha Gururaja Rao and 5 more

Abstract read
In one paragraph

Article in BMC biology, 2026. 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

15 authors.

Veronica Loyo-CelisDepartment of Physiology and Cell Biology, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, United States.
Shridhar SanghviDepartment of Physiology and Cell Biology, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, United States.
Satish K RautDepartment of Physiology and Cell Biology, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, United States.
Hiram Pacheco CastilloDepartamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, UNAM, Cuernavaca, 62210, México.
Jose Luis de la Vega BeltranDepartamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, UNAM, Cuernavaca, 62210, México.
Gerardo OrtaDepartamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, UNAM, Cuernavaca, 62210, México.
Alejandra Montanez-BarraganCenter for Microbe and Immunity Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Aaryan PatelDepartment of Physiology and Cell Biology, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, United States.
Victor Xavier Abonza AmaroLaboratorio Nacional de Microscopía Avanzada, Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México (UNAM), Cuernavaca, 62210, México.
Shubha Gururaja RaoDepartment of Pharmaceutical and Biomedical Sciences, Raabe College of Pharmacy, Ohio Northern University, Ada, OH, 45810, United States.
John C EdwardsNephrology Division, Department of Internal Medicine, St. Louis University, St. Louis, MO, USA.
Santiago Partida-SanchezCenter for Microbe and Immunity Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Alberto DarszonDepartamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, UNAM, Cuernavaca, 62210, México.
Adan GuerreroLaboratorio Nacional de Microscopía Avanzada, Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México (UNAM), Cuernavaca, 62210, México.
Harpreet SinghDepartment of Physiology and Cell Biology, College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, 43210, United States. Harpreet.Singh@osumc.edu.

Funding

Chloride intracellular channels in cardiac mitochondria and their direct role in cardioprotectionR01HL133050 · NHLBI · OHIO STATE UNIVERSITY · PI SINGH, HARPREET · 2016 to 2020
$2.0M
Biophysical properties and role of CLIC6 in cardiomyocyte mitochondriaR03TR004178 · NCATS · OHIO STATE UNIVERSITY · PI SINGH, HARPREET · 2022 to 2022
$158k
Characterization of CLIC2R03TR005313 · NCATS · OHIO STATE UNIVERSITY · PI SINGH, HARPREET · 2025 to 2025
$158k
American Heart Association 23DIVSUP1074277American Heart Association-American Stroke Association 16GRNT29430000American Heart Association-American Stroke Association 965031American Heart Association-American Stroke Association 972077Convocatoria Ciencia de Frontera CF-2023-I-291NCATS NIH HHS R03 TR004178NCATS NIH HHS R03 TR005313NCATS NIH HHS TR004178NHLBI NIH HHS HL133050NHLBI NIH HHS R01 HL133050NIH HHS HD380882PAPIIT/UNAM IN204922
6 · The paper itself

Abstract

backgroundChloride ions (Cl) regulate sperm physiology, influencing spermatogenesis, volume regulation, capacitation, and fertilization processes. They contribute to the maintenance of membrane potential and intracellular pH, both of which are critical for sperm motility and capacitation. Any deviation in Cl homeostasis causes impaired sperm function and male infertility. Although several Cl channels and transporters have been implicated in the Cl homeostasis and osmoregulation of sperm cells, the precise mechanisms and molecular components governing volume regulation during sperm development remain unclear.

methodsWe used a combination of electrophysiological recordings via the patch-clamp technique and biochemical analyses, including western blotting and immunocytochemistry, to demonstrate the functional expression of a novel chloride channel, Chloride Intracellular Channel 4 (CLIC4), in the plasma membrane of sperm cells. To assess physiological roles, we analyzed sperm cells from wild type and null mutant mice (clic4

resultsWe identified previously uncharacterized IAA-94-sensitive chloride currents in mouse sperm cells. Genetic ablation of CLIC4 eliminated these IAA-94-sensitive currents. Notably, CLIC4 regulates cell volume during sperm maturation without altering membrane potential, motility, or the acrosome reaction. CLIC4 activity in sperm cells is modulated by Protein Kinase C (PKC).

conclusionCLIC4 is a key component of the sperm cell volume regulation machinery, modulating Cl fluxes during maturation. These findings provide new insights into the molecular basis of sperm osmoregulation and may inform therapeutic strategies for male infertility.

Indexed as

Chloride ChannelsProtein Kinase CSpermatozoaAnimalsCell SizeMaleMiceMice, KnockoutMitochondrial ProteinsSperm MotilityChloride ChannelsCLIC protein, mouseMitochondrial ProteinsProtein Kinase CCLIC4DevelopmentIAA-94SpermVolume

Identifiers

PMID41715063
PMCPMC13020138

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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.