Evidence map›Paper›PMID 30941132›Full record

ArticleFrontiers in immunology2019

Interaction of Serum-Derived and Internalized C3 With DNA in Human B Cells-A Potential Involvement in Regulation of Gene Transcription.

Mariann Kremlitzka, Alicja A Nowacka, Frida C Mohlin, Pradeep Bompada, Yang De Marinis, Anna M Blom

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

32 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
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  7. Inside job: Roles of intracellular C3.The Journal of allergy and clinical immunology · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. The multiverse of CD46 and oncologic interactions.The Journal of clinical investigation · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. Role of Complement in Liver Diseases.Seminars in liver disease · 2024
    Review
  16. Intracellular C3 protects β-cells from IL-1β-driven cytotoxicity via interaction with Fyn-related kinase.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Complement, complosome, and complotype: A perspective.European journal of immunology · 2023
    Review
  18. Review
  19. Complosome - the intracellular complement system.Nature reviews. Nephrology · 2023
    Review
  20. 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

6 authors at 2 institutions in 1 country.

Mariann KremlitzkaDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Alicja A NowackaDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Frida C MohlinDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Pradeep BompadaGenomics, Diabetes and Endocrinology, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Yang De MarinisGenomics, Diabetes and Endocrinology, Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Anna M BlomDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Lund University · SEMalmö University · SE

Funding

Swedish Research Council
6 · The paper itself

Abstract

Beside its classical role as a serum effector system of innate immunity, evidence is accumulating that complement has an intracellular repertoire of components that provides not only immune defense, but also functions to maintain cellular homeostasis. While complement proteins, mainly the central component C3, have been detected in B cells, their exact function and source remain largely unexplored. In this study, we investigated the expression and origin of intracellular C3 in human B cells together with its role in B cell homeostasis. Our data provide evidence that endogenous expression of C3 is very low in human B cells and, in accordance with the recent publication, the main origin of intracellular C3 is the serum. Interestingly, we found that both serum-derived and purified C3 are able to enter the nucleus of viable B cells, suggesting its potential involvement in regulation of gene transcription. ELISA, gel shift assay, confocal microscopy, and chromatin immunoprecipitation proved that C3 and C3a strongly bind to nuclear DNA, and among the interacting genes there are key factors of lymphocyte development and differentiation. The strong interaction of C3 with histone proteins and its potential ability to induce chromatin rearrangement suggest that C3/C3a might regulate DNA transcription via chromatin remodeling. Our data reveal a novel, hitherto undescribed role of C3 in immune cell homeostasis, which further extends the repertoire how complement links innate and adaptive immunity and regulates basic processes of the cells.

Indexed as

B-LymphocytesCell DifferentiationCell LineCell Line, TumorChromatinComplement C3DNAHEK293 CellsHumansImmunity, InnateJurkat CellsLymphocytesTHP-1 CellsTranscription, GeneticChromatinComplement C3DNAcomplement C3DNAgene transcriptionhistonesinternalization

Identifiers

PMID30941132
PMCPMC6433827
OpenAlexW2923394875

What OpenQuestion holds

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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.