Evidence map›Paper›PMID 22030398›Full record

ArticleThe Journal of biological chemistry2011

Lipocalin-2 Is a chemokine inducer in the central nervous system: role of chemokine ligand 10 (CXCL10) in lipocalin-2-induced cell migration.

Shinrye Lee, Jong-Heon Kim, Jae-Hong Kim, Jung-Wan Seo, Hyung-Soo Han, Won-Ha Lee, Kiyoshi Mori, Kazuwa Nakao, Jonathan Barasch, Kyoungho Suk

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

103 citing papers in PubMed, 169 citations in OpenAlex.

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43 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 3 countries.

Shinrye LeeDepartment of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Jong-Heon KimDepartment of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Jae-Hong KimDepartment of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Jung-Wan SeoDepartment of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Hyung-Soo HanDepartment of Physiology, Brain Science & Engineering Institute, Cell and Matrix Research Institute, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Won-Ha LeeDepartments of School of Life Sciences and Biotechnology, Kyungpook National University School of Medicine, Daegu 700-422, Korea.
Kiyoshi MoriDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
Kazuwa NakaoDepartment of Medicine and Clinical Science, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
Jonathan BaraschDepartment of Medicine, College of Physicians and Surgeons, Columbia University, New York, New York 10027.
Kyoungho SukDepartment of Pharmacology, Kyungpook National University School of Medicine, Daegu 700-422, Korea. Electronic address: ksuk@knu.ac.kr.
Kyungpook National University · KRKyoto University · JPColumbia University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The secreted protein lipocalin-2 (LCN2) has been implicated in diverse cellular processes, including cell morphology and migration. Little is known, however, about the role of LCN2 in the CNS. Here, we show that LCN2 promotes cell migration through up-regulation of chemokines in brain. Studies using cultured glial cells, microvascular endothelial cells, and neuronal cells suggest that LCN2 may act as a chemokine inducer on the multiple cell types in the CNS. In particular, up-regulation of CXCL10 by JAK2/STAT3 and IKK/NF-κB pathways in astrocytes played a pivotal role in LCN2-induced cell migration. The cell migration-promoting activity of LCN2 in the CNS was verified in vivo using mouse models. The expression of LCN2 was notably increased in brain following LPS injection or focal injury. Mice lacking LCN2 showed the impaired migration of astrocytes to injury sites with a reduced CXCL10 expression in the neuroinflammation or injury models. Thus, the LCN2 proteins, secreted under inflammatory conditions, may amplify neuroinflammation by inducing CNS cells to secrete chemokines such as CXCL10, which recruit additional inflammatory cells.

Indexed as

Gene Expression RegulationAcute-Phase ProteinsAnimalsAstrocytesBrainCell MovementChemokine CXCL10ChemokinesCulture Media, ConditionedHumansInflammationLipocalin-2LipocalinsMiceMice, TransgenicOncogene ProteinsAcute-Phase ProteinsChemokine CXCL10ChemokinesCulture Media, ConditionedCXCL10 protein, humanCxcl10 protein, mouseLCN2 protein, humanLcn2 protein, mouseLipocalin-2LipocalinsOncogene ProteinsProto-Oncogene ProteinsSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID22030398
PMCPMC3243551
OpenAlexW2012229822

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.