Evidence map›Paper›PMID 25468721›Full record

ArticleImmunobiology2015

Epididymal C4b-binding protein is processed and degraded during transit through the duct and is not essential for fertility.

Mayumi I Nonaka, Eva Zsigmond, Akihiko Kudo, Hayato Kawakami, Kaoru Yoshida, Manabu Yoshida, Natsuko Kawano, Kenji Miyado, Masaru Nonaka, Rick A Wetsel

Open access · greenAbstract read
In one paragraph

Article in Immunobiology, 2015. 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
0.7field-weighted citation impact, top 29% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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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

10 authors at 4 institutions in 2 countries.

Mayumi I NonakaDepartment of Biological Sciences, The University of Tokyo, Tokyo, Japan. Electronic address: nmayumi@bs.s.u-tokyo.ac.jp.
Eva ZsigmondThe Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, USA.
Akihiko KudoDepartment of Anatomy, Kyorin University School of Medicine, Mitaka, Japan.
Hayato KawakamiDepartment of Anatomy, Kyorin University School of Medicine, Mitaka, Japan.
Kaoru YoshidaBiomedical Engineering Center, Toin University of Yokohama, Yokohama, Japan.
Manabu YoshidaMisaki Marine Biological Station, The University of Tokyo, Miura, Japan.
Natsuko KawanoDepartment of Reproductive Biology, National Center for Child Health and Development, Tokyo, Japan.
Kenji MiyadoDepartment of Reproductive Biology, National Center for Child Health and Development, Tokyo, Japan.
Masaru NonakaDepartment of Biological Sciences, The University of Tokyo, Tokyo, Japan.
Rick A WetselThe Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, USA.
Brown Foundation · USKyorin University · JPNational Center For Child Health and Development · JPThe University of Tokyo · JP

Funding

Mouse C4b-binding Protein in Adaptive ImmunityR03AI068795 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WETSEL, RICK A. · 2006 to 2007
$146k
NIAID NIH HHS R03 AI068795NIAID NIH HHS R03AI068795
6 · The paper itself

Abstract

C4b-binding protein (C4BP) is known as one of the circulating complement regulators that prevents excessive activation of the host-defense complement system. We have reported previously that C4BP is expressed abundantly in the rodent epididymis, one of the male reproductive organs connecting the testis and vas deferens, where immature spermatozoa acquire their motility and fertilizing ability during their transit through the duct. Epididymal C4BP (EpC4BP) is synthesized androgen-dependently by the epithelial cells, secreted into the lumen, and bound to the outer membrane of the passing spermatozoa. In this study, we found that EpC4BP is secreted as a large oligomer, similar to the serum C4BP, but is digested during the epididymal transit and is almost lost from both the luminal fluid and the sperm surface in the vas deferens. Such a processing pattern is not known in serum C4BP, suggesting that EpC4BP and serum C4BP might have different functional mechanisms, and that there is a novel function of EpC4BP in reproduction. In addition, the disappearance of EpC4BP from the sperm surface prior to ejaculation suggests that EpC4BP works only in the epididymis and would not work in the female reproductive tract to protect spermatozoa from complement attack. Next, we generated C4BP-deficient (C4BP-/-) mice to examine the possible role of EpC4BP in reproduction. However, the C4BP-/- mice were fertile and no significant differences were observed between the C4BP-/- and wild-type mouse spermatozoa in terms of morphology, motility, and rate of the spontaneous acrosome reaction. These results suggest that EpC4BP is involved in male reproduction, but not essential for sperm maturation.

Indexed as

FertilityAcrosomeAnimalsComplement C4b-Binding ProteinEpididymisFemaleGene ExpressionGene OrderGene TargetingMaleMiceMice, KnockoutModels, AnimalOrgan SpecificityPhenotypeProtein TransportComplement C4b-Binding ProteinC4BPComplementEpididymisGene targetingProcessingReproductionSperm maturation

Identifiers

PMID25468721
PMCPMC4355379
OpenAlexW2092877846

What OpenQuestion 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 OpenQuestion graph.