Evidence map›Paper›PMID 35546365›Full record

ArticleCellular and molecular life sciences : CMLS2022

Alternative translation and retrotranslocation of cytosolic C3 that detects cytoinvasive bacteria.

Mariann Kremlitzka, Lucie Colineau, Alicja A Nowacka, Frida C Mohlin, Katarzyna Wozniak, Anna M Blom, Ben C King

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Inside job: Roles of intracellular C3.The Journal of allergy and clinical immunology · 2025
    Review
  4. Complement C3 Activation in the Human Retinal Pigment Epithelium.Investigative ophthalmology & visual science · 2025
    Article
  5. Review
  6. Article
  7. Complement and T cell activation in transplantation.Transplantation reviews (Orlando, Fla.) · 2025
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. 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
  13. Review
  14. Review
  15. Complement, complosome, and complotype: A perspective.European journal of immunology · 2023
    Review
  16. Complosome - the intracellular complement system.Nature reviews. Nephrology · 2023
    Review
  17. Review
  18. 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 2 countries.

Mariann Kremlitzka *Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Lucie Colineau *Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.ORCID http://orcid.org/0000-0001-6221-0765
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.
Katarzyna WozniakDivision of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.
Anna M Blom *Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden. anna.blom@med.lu.se.ORCID http://orcid.org/0000-0002-1348-1734
Ben C King *Division of Medical Protein Chemistry, Department of Translational Medicine, Lund University, Malmö, Sweden.ORCID http://orcid.org/0000-0001-6776-8741
Lund University · SEEötvös Loránd University · HU

Funding

Knut och Alice Wallenbergs Stiftelse Wallenberg ScholarStiftelsen för Strategisk Forskning Dnr IRC15-0067Vetenskapsrådet 2009-1039Vetenskapsrådet 2018-02392Wellcome Trust 109055
6 · The paper itself

Abstract

Complement C3 was originally regarded as a serum effector protein, although recent data has emerged suggesting that intracellular C3 can also regulate basic cellular processes. Despite the growing interest in intracellular C3 functions, the mechanism behind its generation has not been demonstrated. In this study we show that C3 can be expressed from an alternative translational start site, resulting in C3 lacking the signal peptide, which is therefore translated in the cytosol. In contrast to the secreted form, alternatively translated cytosolic C3 is not glycosylated, is present mainly in a reduced state, and is turned over by the ubiquitin-proteasome system. C3 can also be retrotranslocated from the endoplasmic reticulum into the cytosol, structurally resembling secreted C3. Finally, we demonstrate that intracellular cytosolic C3 can opsonize invasive Staphylococcus aureus within epithelial cell, slowing vacuolar escape as well as impacting bacterial survival on subsequent exposure to phagocytes. Our work therefore reveals the existence and origin of intracellular, cytosolic C3, and demonstrates functions for cytosolic C3 in intracellular detection of cytoinvasive pathogens.

Indexed as

Complement C3Proteasome Endopeptidase ComplexBacteriaCytosolEndoplasmic ReticulumComplement C3Proteasome Endopeptidase ComplexCellular traffickingComplement factor C3Intracellular complementPathogen sensing

Identifiers

PMID35546365
PMCPMC9095555
OpenAlexW4280501787

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.