Evidence map›Paper›PMID 19794905›Full record

ReviewOxidative medicine and cellular longevity

Nitric oxide and cyclic nucleotides: their roles in junction dynamics and spermatogenesis.

Nikki P Y Lee, C Yan Cheng

Open access · hybridAbstract readReview
In one paragraph

Review in Oxidative medicine and cellular longevity. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.6field-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

12 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. The Interaction of NO and HAnimals : an open access journal from MDPI · 2022
    Article
  6. New Insight into Molecular and Hormonal Connection in Andrology.International journal of molecular sciences · 2021
    Review
  7. Oxidative DNA Damage to Sperm Cells and Peripheral Blood Leukocytes in Infertile Men.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Ca(2+)-modulated membrane guanylate cyclase in the testes.Molecular and cellular biochemistry · 2010
    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

2 authors at 2 institutions in 3 countries.

Nikki P Y LeeDepartment of Medicine/Surgery, University of Hong Kong, Queen Mary Hospital, Hong Kong, China. nikkilee@hkucc.hku.hk
C Yan Cheng
Population Council · USQueen Mary Hospital · CN

Funding

SPECIALIZED CONTRACEPTIVE DEVELOPMENT RESEARCH CENTERU54HD029990 · NICHD · POPULATION COUNCIL · PI WARE, REGINE SITRUK · 1992 to 2016
$27.7M
Junction Dynamics and Male Fertility RegulationU01HD045908 · NICHD · POPULATION COUNCIL · PI CHENG, C. YAN · 2004 to 2008
$1.3M
NICHD NIH HHS U01 HD045908NICHD NIH HHS U54 HD029990NICHD NIH HHS U54 HD29990 PROJECT 3
6 · The paper itself

Abstract

Spermatogenesis is a highly complicated process in which functional spermatozoa (haploid, 1n) are generated from primitive mitotic spermatogonia (diploid, 2n). This process involves the differentiation and transformation of several types of germ cells as spermatocytes and spermatids undergo meiosis and differentiation. Due to its sophistication and complexity, testis possesses intrinsic mechanisms to modulate and regulate different stages of germ cell development under the intimate and indirect cooperation with Sertoli and Leydig cells, respectively. Furthermore, developing germ cells must translocate from the basal to the apical (adluminal) compartment of the seminiferous epithelium. Thus, extensive junction restructuring must occur to assist germ cell movement. Within the seminiferous tubules, three principal types of junctions are found namely anchoring junctions, tight junctions, and gap junctions. Other less studied junctions are desmosome-like junctions and hemidesmosome junctions. With these varieties of junction types, testes are using different regulators to monitor junction turnover. Among the uncountable junction modulators, nitric oxide (NO) is a prominent candidate due to its versatility and extensive downstream network. NO is synthesized by nitric oxide synthase (NOS). Three traditional NOS, specified as endothelial NOS (eNOS), inducible NOS (iNOS), and neuronal NOS (nNOS), and one testis-specific nNOS (TnNOS) are found in the testis. For these, eNOS and iNOS were recently shown to have putative junction regulation properties. More important, these two NOSs likely rely on the downstream soluble guanylyl cyclase/cGMP/protein kinase G signaling pathway to regulate the structural components at the tight junctions and adherens junctions in the testes. Apart from the involvement in junction regulation, NOS/NO also participates in controlling the levels of cytokines and hormones in the testes. On the other hand, NO is playing a unique role in modulating germ cell viability and development, and indirectly acting on some aspects of male infertility and testicular pathological conditions. Thus, NOS/NO bears an irreplaceable role in maintaining the homeostasis of the microenvironment in the seminiferous epithelium via its different downstream signaling pathways.

Indexed as

AnimalsHumansIntercellular JunctionsMaleNitric OxideNitric Oxide SynthaseNucleotides, CyclicSpermatogenesisTestisNitric OxideNitric Oxide SynthaseNucleotides, Cyclicintegral membrane proteinsnitric oxidenitric oxide synthasespermatogenesistestes

Identifiers

PMID19794905
PMCPMC2715196
OpenAlexW2128788909

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.