Evidence map›Paper›PMID 31341044›Full record

ArticleJournal of virology2019

The Interferon-Inducible Proteoglycan Testican-2/SPOCK2 Functions as a Protective Barrier against Virus Infection of Lung Epithelial Cells.

Narae Ahn, Woo-Jong Kim, Nari Kim, Han Wook Park, Seung-Woo Lee, Joo-Yeon Yoo

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Testican-2 (SPOCK2): A multifunctional matricellular regulator.Matrix biology : journal of the International Society for Matrix Biology · 2026
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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

6 authors at 1 institution in 1 country.

Narae AhnDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Woo-Jong KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Nari KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Han Wook ParkDepartment of Integrative Biosciences & Biotechnology, Pohang University of Science and Technology, Pohang, Republic of Korea.
Seung-Woo LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Joo-Yeon YooDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea jyoo@postech.ac.kr.
Pohang University of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteoglycans function not only as structural components of the extracellular compartment but also as regulators of various cellular events, including cell migration, inflammation, and infection. Many microbial pathogens utilize proteoglycans to facilitate adhesion and invasion into host cells. Here we report a secreted form of a novel heparan sulfate proteoglycan that functions against virus infection. The expression of SPOCK2/testican-2 was significantly induced in virus-infected lungs or in interferon (IFN)-treated alveolar lung epithelial cells. Overexpression from a SPOCK2 expression plasmid alone or the treatment of cells with recombinant SPOCK2 protein efficiently blocked influenza virus infection at the step of viral attachment to the host cell and entry. Moreover, mice treated with purified SPOCK2 were protected against virus infection. Sialylated glycans and heparan sulfate chains covalently attached to the SPOCK2 core protein were critical for its antiviral activity. Neuraminidase (NA) of influenza virus cleaves the sialylated moiety of SPOCK2, thereby blocking its binding to the virus. Our data suggest that IFN-induced SPOCK2 functions as a decoy receptor to bind and block influenza virus infection, thereby restricting entry of the infecting virus into neighboring cells.

Indexed as

Alveolar Epithelial CellsAnimalsAntiviral AgentsCell LineDisease Models, AnimalDisease ResistanceFemaleGene ExpressionHeparan Sulfate ProteoglycansHost-Pathogen InteractionsHumansInfluenza A virusMiceProteoglycansRecombinant ProteinsVirus AttachmentAntiviral AgentsHeparan Sulfate ProteoglycansProteoglycansRecombinant ProteinsSPOCK2 protein, humanantiviralextracellular matrixinfluenzaproteoglycanSPOCK2

Identifiers

PMID31341044
PMCPMC6798107
OpenAlexW2963217750

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.