Evidence map›Paper›PMID 25866637›Full record

ArticleImmunity, inflammation and disease2015

Serglycin is part of the secretory repertoire of LPS-activated monocytes.

Ingrid Benedicte M Kolseth, Trine Marita Reine, Tram Thu Vuong, Astri Jeanette Meen, Qiong Fan, Trond Geir Jenssen, Line Mariann Grønning-Wang, Svein Olav Kolset

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Differential transcriptomic and metabolomic landscape between human hearts donated after cardiac vs brain death.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2026
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  11. STAT3 regulates SRGN and promotes metastasis of nasopharyngeal carcinoma through the FoxO1-miR-148a-5p-CREB1 axis.Laboratory investigation; a journal of technical methods and pathology · 2022
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  15. Proteoglycans as Mediators of Cancer Tissue Mechanics.Frontiers in cell and developmental biology · 2020
    Review
  16. Article
  17. 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

8 authors at 2 institutions in 1 country.

Ingrid Benedicte M KolsethDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Trine Marita ReineDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Tram Thu VuongDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Astri Jeanette MeenDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Qiong FanDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Trond Geir JenssenDepartment of Transplant Medicine, Section of Nephrology, Oslo University Hospital Rikshospitalet, Oslo, Norway ; Metabolic and Renal Research Group, UiT The Arctic University of Norway Tromsø, Norway.
Line Mariann Grønning-WangDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
Svein Olav KolsetDepartment of Nutrition, Institute of Basic Medical Sciences, University of Oslo Oslo, Norway.
University of Oslo · NOUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monocytes play multiple roles in the immune system, and are active in both acute and chronic diseases. Patients exposed to bacterial infections depend on monocytes in defense reactions, but excessive immune reactions may also cause morbidity through systemic inflammatory responses. Few studies have addressed the importance of proteoglycans, and in particular, the hematopoietic serglycin, in such monocyte immune reactions. Adherent primary monocytes were cultured in absence and presence of LPS. Media were analyzed by ELISA for detection of serglycin. Lysed cell fractions were used to determine the mRNA level of serglycin. Monocytes were also cultured on chamber slides to investigate if serglycin could be detected intracellularly by immunocytochemistry. Monocytes secreted serglycin, and LPS-stimulation increased the secretion. Secretion of inflammatory cytokines increased to a larger extent than serglycin. mRNA levels of serglycin were also increased, suggesting both increased expression and secretion. Immunocytochemistry revealed the presence of serglycin in intracellular vesicles, many destined for secretion. Serglycin containing vesicles increased in number and size when the cells were exposed to LPS. Intracellular vesicle localization and secretion of the proteoglycan serglycin is shown for the first time in primary human monocytes. Monocyte activation by LPS increased the expression and secretion of serglycin, suggesting roles for serglycin in inflammatory processes.

Indexed as

Cytokinesinflammationlipopolysaccharidemonocytesserglycin

Identifiers

PMID25866637
PMCPMC4386912
OpenAlexW1738649838

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.