Evidence map›Paper›PMID 29047397›Full record

ArticleParasites & vectors2017

Tyrosine kinase 4 is involved in the reproduction of the platyhelminth parasite Schistosoma japonicum.

Han Ding, Fengchun Liu, Lulu Zhu, Fei Wu, Quan Liu, Siyu He, Wei Shao, Yinan Du, Cuiping Ren, Jijia Shen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Chemical modulation ofWellcome open research · 2023
    Article
  5. Protein Kinases: Potential Drug Targets AgainstFrontiers in cellular and infection microbiology · 2021
    Review
  6. 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

11 authors at 1 institution in 1 country.

Han DingDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Fengchun LiuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Lulu ZhuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Fei WuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Quan LiuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Siyu HeDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Wei ShaoDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Yinan DuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Cuiping RenDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China.
Jijia ShenDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China. shenjijia@hotmail.com.
Miao LiuDepartment of Microbiology and Parasitology, Anhui Provincial Laboratory of Microbiology and Parasitology, School of Basic Medical Sciences, 81#Meishan Road, Hefei, Anhui, 230032, People's Republic of China. iammiaoliu@126.com.
Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchistosomiasis is one of the most common parasitic diseases affecting millions of humans and animals worldwide. Understanding the signal transduction pathways and the molecular basis of reproductive regulation in schistosomes is critically important for developing new strategies for preventing and treating these infections. Syk kinases regulate the proliferation, differentiation, morphogenesis, and survival of various types of cells and have been identified in invertebrates. Tyrosine kinase 4 (TK4), a member of the Syk kinase family, plays a pivotal role in gametogenesis in S. mansoni, affecting the development of the testis and ovaries in this parasite. The role of TK4, however, in the reproduction of S. japonicum is poorly understood.

methodsHere, the complete coding sequence of TK4 gene in S. japonicum (SjTK4) was cloned and characterized. The expression of SjTK4 was analyzed at different life-cycle stages and in various tissues of S. japonicum by qPCR. Piceatannol, a Syk kinase inhibitor, was applied to S. japonicum in vitro. The piceatannol-induced morphological changes of the parasites were observed using confocal laser scanning microscopy and the alterations in important egg-shell synthesis-related genes were examined using qPCR analyses.

resultsSjTK4 mRNA was differentially expressed throughout the life-cycle of S. japonicum. SjTK4 mRNA was highly expressed in the ovary and testis of S. japonicum, with the level of gene expression significantly higher in males than in females. The expression levels of some important egg-shell synthesis related genes were higher in the piceatannol-treated groups than in the vehicle-treated control group and the number of eggs and germ cells also decreased in a concentration-dependent manner. Importantly, large pore-like structures can be found in the testis and ovaries of males and females after treating with piceatannol.

conclusionThe results suggest that SjTK4 may play an important role in regulating gametogenesis of S. japonicum. The findings may help better understand the fundamental biology of S. japonicum. Moreover, the effect of S. japonicum treatment by piceatannol provides us with a new idea that inhibition of SjTK4 signaling pathway can effectively retard the development of the testis and ovaries.

Indexed as

AnimalsCoinfectionFemaleHumansMaleMiceProtein-Tyrosine KinasesReproductionSchistosoma japonicumSchistosomiasis japonicaStilbenes3,3',4,5'-tetrahydroxystilbeneProtein-Tyrosine KinasesStilbenesPiceatannolReproductionSchistosoma japonicumSjTK4

Identifiers

PMID29047397
PMCPMC5648501
OpenAlexW2766925326

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.