Evidence map›Paper›PMID 31263154›Full record

ArticleScientific reports2019

Expression of neuropeptide Y is increased in an activated human HSC cell line.

Wufei Dai, Yang Liu, Yali Zhang, Yufeng Sun, Changjiang Sun, Yu Zhang, Xiufang Lv

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. The role of PYY in improving insulin resistance.Frontiers in endocrinology · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. GPCRs and fibroblast heterogeneity in fibroblast-associated diseases.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Review
  6. Review
  7. Review
  8. Review
  9. Proteomic Changes of Activated Hepatic Stellate Cells.International journal of molecular sciences · 2021
    Article
  10. Article
  11. 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

7 authors at 2 institutions in 1 country.

Wufei DaiBasic Medical Research Centre, Medical College of Nantong University, Nantong, China.
Yang LiuBasic Medical Research Centre, Medical College of Nantong University, Nantong, China.
Yali ZhangDepartment of Biochemistry, Medical College of Nantong University, Nantong, China.
Yufeng SunBasic Medical Research Centre, Medical College of Nantong University, Nantong, China.
Changjiang SunDepartment of Clinical Laboratory, Affiliated Hospital of Nantong University, Nantong, China.
Yu ZhangDepartment of hepatobiliary Surgery, Affiliated Hospital of Nantong University, Nantong, China.
Xiufang LvBasic Medical Research Centre, Medical College of Nantong University, Nantong, China. 2005lxf801@163.com.
Nantong University · CNAffiliated Hospital of Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropeptide Y (NPY) is an abundant neuropeptide in the mammalian central and peripheral nervous systems. Transgenic mice overexpressing NPY in noradrenergic neurons have increased level of hepatic triglycerides, fatty acids and cholesterol, which contributed to the development of hepatosteatosis. However, the roles of NPY in the activation of hepatic stellate cells (HSCs) and the underlying mechanisms remain unclear. This study aimed to investigate the expression and secretion of NPY in human immortalized HSC LX-2 cells and the regulatory function of NPY on the fibrogenic response in LX-2 cells, to explore the potential association between NPY and LX-2 activation. The results showed an increase in the expression and secretion of NPY(1-36) in activated LX-2 cells. Both endogenous and exogenous NPY(1-36) induced the phosphorylation of mTOR, p70S6K, and 4EBP1 and promoted the fibrogenic response via NPY Y1 receptor subtype (NPY1R), as these responses were blocked by either an NPY1R antagonist (BIBP3226) or NPY1R knockdown. Moreover, NPY(1-36) serum levels were increased in patients with liver cirrhosis (LC) and hepatocellular carcinoma (HCC) and presented a positive relationship with MELD scores in LC patients. These findings suggest that immortalized HSCs LX-2 have the potential to produce NPY(1-36). High serum levels of NPY(1-36) is correlated with hepatic dysfunction in cirrhotic patients.

Indexed as

Adaptor Proteins, Signal TransducingArginineCell Cycle ProteinsCell Line, TransformedFibrosisHepatic Stellate CellsHumansNeuropeptide YPhosphorylationReceptors, Neuropeptide YRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine KinasesAdaptor Proteins, Signal TransducingArginineBIBP 3226Cell Cycle ProteinsEIF4EBP1 protein, humanMTOR protein, humanNeuropeptide Yneuropeptide Y-Y1 receptorReceptors, Neuropeptide YRibosomal Protein S6 Kinases, 70-kDaTOR Serine-Threonine Kinases

Identifiers

PMID31263154
PMCPMC6602956
OpenAlexW2956110875

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.