Evidence map›Paper›PMID 21482758›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Cysteine-rich secretory protein 4 is an inhibitor of transient receptor potential M8 with a role in establishing sperm function.

Gerard M Gibbs, Gerardo Orta, Thulasimala Reddy, Adam J Koppers, Pablo Martínez-López, José Luis de la Vega-Beltràn, Jennifer C Y Lo, Nicholas Veldhuis, Duangporn Jamsai, Peter McIntyre and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

59 citing papers in PubMed, 109 citations in OpenAlex.

  1. Review
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  7. Genetic mutation ofLife science alliance · 2024
    Article
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  13. Chemical synthesis ofRSC chemical biology · 2022
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. The Sertoli cell expressed gene secernin-1 (Scrn1) is dispensable for male fertility in the mouse.Developmental dynamics : an official publication of the American Association of Anatomists · 2021
    Article
  19. Article
  20. 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

12 authors at 4 institutions in 2 countries.

Gerard M GibbsDepartment of Anatomy and Developmental Biology, Monash University, VIC 3800, Australia.
Gerardo Orta
Thulasimala Reddy
Adam J Koppers
Pablo Martínez-López
José Luis de la Vega-Beltràn
Jennifer C Y Lo
Nicholas Veldhuis
Duangporn Jamsai
Peter McIntyre
Alberto Darszon
Moira K O'Bryan
Universidad Nacional Autónoma de México · MXUniversity of Melbourne · AUAustralian Research Council · AUMonash University · AU

Funding

Sperm Ca2+ Signaling and Energy Pathways in basic science and ARTR01HD038082 · NICHD · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI VISCONTI, PABLO E. · 2000 to 2025
$6.5M
NICHD NIH HHS R01 HD038082NICHD NIH HHS R01 HD038082-07A1
6 · The paper itself

Abstract

The cysteine-rich secretory proteins (CRISPs) are a group of four proteins in the mouse that are expressed abundantly in the male reproductive tract, and to a lesser extent in other tissues. Analysis of reptile CRISPs and mouse CRISP2 has shown that CRISPs can regulate cellular homeostasis via ion channels. With the exception of the ability of CRISP2 to regulate ryanodine receptors, the in vivo targets of mammalian CRISPs function are unknown. In this study, we have characterized the ion channel regulatory activity of epididymal CRISP4 using electrophysiology, cell assays, and mouse models. Through patch-clamping of testicular sperm, the CRISP4 CRISP domain was shown to inhibit the transient receptor potential (TRP) ion channel TRPM8. These data were confirmed using a stably transfected CHO cell line. TRPM8 is a major cold receptor in the body, but is found in other tissues, including the testis and on the tail and head of mouse and human sperm. Functional assays using sperm from wild-type mice showed that TRPM8 activation significantly reduced the number of sperm undergoing the progesterone-induced acrosome reaction following capacitation, and that this response was reversed by the coaddition of CRISP4. In accordance, sperm from Crisp4 null mice had a compromised ability to undergo to the progesterone-induced acrosome reaction. Collectively, these data identify CRISP4 as an endogenous regulator of TRPM8 with a role in normal sperm function.

Indexed as

Acrosome ReactionAnimalsCHO CellsCricetinaeCricetulusHumansMaleMiceMice, KnockoutProgesteroneProgestinsSeminal Plasma ProteinsSpermatozoaTRPM Cation Channelscysteine-rich secretory protein 4, mouseProgesteroneProgestinsSeminal Plasma ProteinsTRPM8 protein, mouseTRPM Cation Channels

Identifiers

PMID21482758
PMCPMC3084142
OpenAlexW2082975959

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.