PreprintCited by 6Ferroptosis and cancer prognosisNeonatal and Maternal InfectionsIron Metabolism and Disorders

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Unveiling the Crucial Role of Ferroptosis in Host Resistance to Streptococcus agalactiae Infection

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Preprint — published as 10.1038/s41420-024-02189-8

Abstract

IL-1β represents an important inflammatory factor involved in the host response against GBS infection. Prior research has suggested a potential involvement of IL-1β in the process of ferroptosis. However, the relationship between IL-1β and ferroptosis in the context of anti-GBS infection remains uncertain. This research demonstrates that the significance of ferroptosis in the host's immune defense against GBS infection in a mouse model of abdominal infection, with peritoneal macrophages identified as the primary cells undergoing ferroptosis. Subsequent studies have shown that IL-1β promotes lipid oxidation in macrophages by upregulating pathways associated with lipid oxidation. Concurrently, IL-1β is not only involved in the initiation of ferroptosis in macrophages, but its production is intricately linked to the onset of ferroptosis. Ultimately, we posit that ferroptosis acts as a crucial initiating factor in the host response to GBS infection, with IL-1β playing a significant role in the resistance to infection by serving as a key inducer of ferroptosis.

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  1. S.M. Hansen, N. Uldbjerg, M. Kilian, and U.B. Sorensen, Dynamics of Streptococcus agalactiae colonization in women during and after pregnancy and in their infants. J Clin Microbiol 42 (2004) 83–9. · DOI
  2. C. Biondo, G. Mancuso, A. Midiri, G. Signorino, M. Domina, V. Lanza Cariccio, N. Mohammadi, M. Venza, I. Venza, G. Teti, and C. Beninati, The interleukin-1beta/CXCL1/2/neutrophil axis mediates host protection against group B streptococcal infection. Infect Immun 82 (2014) 4508–17. · DOI
  3. T. Persichini, N. Maio, M.C. di Patti, G. Rizzo, S. Toscano, M. Colasanti, and G. Musci, Interleukin-1beta induces ceruloplasmin and ferroportin-1 gene expression via MAP kinases and C/EBPbeta, AP-1, and NF-kappaB activation. Neurosci Lett 484 (2010) 133–8. · DOI
  4. Z. Sun, W. Huang, Y. Zheng, P. Liu, W. Yang, Z. Guo, D. Kong, Q. Lv, X. Zhou, Z. Du, H. Jiang, and Y. Jiang, Fpr2/CXCL1/2 Controls Rapid Neutrophil Infiltration to Inhibit Streptococcus agalactiae Infection. Frontiers in Immunology 12 (2021).
  5. J. Li, F. Cao, H.L. Yin, Z.J. Huang, Z.T. Lin, N. Mao, B. Sun, and G. Wang, Ferroptosis: past, present and future. Cell Death Dis 11 (2020) 88. · DOI · Paper page
  6. Q. Liu, J. Wu, X. Zhang, X. Wu, Y. Zhao, and J. Ren, Iron homeostasis and disorders revisited in the sepsis. Free Radic Biol Med 165 (2021) 1–13. · DOI
  7. G. Corna, L. Campana, E. Pignatti, A. Castiglioni, E. Tagliafico, L. Bosurgi, A. Campanella, S. Brunelli, A.A. Manfredi, P. Apostoli, L. Silvestri, C. Camaschella, and P. Rovere-Querini, Polarization dictates iron handling by inflammatory and alternatively activated macrophages. Haematologica 95 (2010) 1814–22. · DOI · Paper page
  8. C.B. Billesbolle, C.M. Azumaya, R.C. Kretsch, A.S. Powers, S. Gonen, S. Schneider, T. Arvedson, R.O. Dror, Y. Cheng, and A. Manglik, Structure of hepcidin-bound ferroportin reveals iron homeostatic mechanisms. Nature 586 (2020) 807–811. · DOI · Paper page
  9. F. Du, Z.M. Qian, Q. Gong, Z.J. Zhu, L. Lu, and Y. Ke, The iron regulatory hormone hepcidin inhibits expression of iron release as well as iron uptake proteins in J774 cells. J Nutr Biochem 23 (2012) 1694–700. · DOI
  10. J.M. Muriuki, A.J. Mentzer, G. Band, J.J. Gilchrist, T. Carstensen, S.A. Lule, M.M. Goheen, F. Joof, W. Kimita, R. Mogire, C.L. Cutland, A. Diarra, A. Rautanen, C. Pomilla, D. Gurdasani, K. Rockett, N. Mturi, F.M. Ndungu, J.A.G. Scott, S.B. Sirima, A. Morovat, A.M. Prentice, S.A. Madhi, E.L. Webb, A.M. Elliott, P. Bejon, M.S. Sandhu, A.V.S. Hill, D.P. Kwiatkowski, T.N. Williams, C. Cerami, and S.H. Atkinson, The ferroportin Q248H mutation protects from anemia, but not malaria or bacteremia. Sci Adv 5 (2019) eaaw0109. · DOI · Paper page
  11. N.K. Shanmugam, K. Chen, and B.J. Cherayil, Commensal Bacteria-induced Interleukin 1beta (IL-1beta) Secreted by Macrophages Up-regulates Hepcidin Expression in Hepatocytes by Activating the Bone Morphogenetic Protein Signaling Pathway. J Biol Chem 290 (2015) 30637–47. · DOI
  12. P.J. Schmidt, Regulation of Iron Metabolism by Hepcidin under Conditions of Inflammation. J Biol Chem 290 (2015) 18975–83. · DOI
  13. Y. Kanamori, M. Murakami, M. Sugiyama, O. Hashimoto, T. Matsui, and M. Funaba, Interleukin-1beta (IL-1beta) transcriptionally activates hepcidin by inducing CCAAT enhancer-binding protein delta (C/EBPdelta) expression in hepatocytes. J Biol Chem 292 (2017) 10275–10287. · DOI
  14. X. Chen, R. Kang, G. Kroemer, and D. Tang, Ferroptosis in infection, inflammation, and immunity. J Exp Med 218 (2021). · DOI
  15. T. Hirschhorn, and B.R. Stockwell, The development of the concept of ferroptosis. Free Radic Biol Med 133 (2019) 130–143. · DOI · Paper page
  16. B. Zhou, J. Liu, R. Kang, D.J. Klionsky, G. Kroemer, and D. Tang, Ferroptosis is a type of autophagy-dependent cell death. Seminars in Cancer Biology 66 (2020) 89–100. · DOI
  17. E. Park, and S.W. Chung, ROS-mediated autophagy increases intracellular iron levels and ferroptosis by ferritin and transferrin receptor regulation. Cell Death & Disease 10 (2019). · DOI
  18. S. Dolma, S.L. Lessnick, W.C. Hahn, and B.R. Stockwell, Identification of genotype-selective antitumor agents using synthetic lethal chemical screening in engineered human tumor cells. Cancer Cell 3 (2003) 285–96. · DOI · Paper page
  19. H. Yuk, M. Abdullah, D.H. Kim, H. Lee, and S.J. Lee, Necrostatin-1 Prevents Ferroptosis in a RIPK1- and IDO-Independent Manner in Hepatocellular Carcinoma. Antioxidants (Basel) 10 (2021).
  20. A. Donovan, A. Brownlie, Y. Zhou, J. Shepard, S.J. Pratt, J. Moynihan, B.H. Paw, A. Drejer, B. Barut, A. Zapata, T.C. Law, C. Brugnara, S.E. Lux, G.S. Pinkus, J.L. Pinkus, P.D. Kingsley, J. Palis, M.D. Fleming, N.C. Andrews, and L.I. Zon, Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter. Nature 403 (2000) 776–81. · DOI · Paper page
  21. H.H. Dar, Y.Y. Tyurina, K. Mikulska-Ruminska, I. Shrivastava, H.C. Ting, V.A. Tyurin, J. Krieger, C.M. St Croix, S. Watkins, E. Bayir, G. Mao, C.R. Armbruster, A. Kapralov, H. Wang, M.R. Parsek, T.S. Anthonymuthu, A.F. Ogunsola, B.A. Flitter, C.J. Freedman, J.R. Gaston, T.R. Holman, J.M. Pilewski, J.S. Greenberger, R.K. Mallampalli, Y. Doi, J.S. Lee, I. Bahar, J.M. Bomberger, H. Bayir, and V.E. Kagan, Pseudomonas aeruginosa utilizes host polyunsaturated phosphatidylethanolamines to trigger theft-ferroptosis in bronchial epithelium. J Clin Invest 128 (2018) 4639–4653. · DOI · Paper page
  22. J. Ousingsawat, R. Schreiber, E. Gulbins, M. Kamler, and K. Kunzelmann, P. aeruginosa Induced Lipid Peroxidation Causes Ferroptotic Cell Death in Airways. Cell Physiol Biochem 55 (2021) 590–604. · DOI
  23. E.P. Amaral, D.L. Costa, S. Namasivayam, N. Riteau, O. Kamenyeva, L. Mittereder, K.D. Mayer-Barber, B.B. Andrade, and A. Sher, A major role for ferroptosis in Mycobacterium tuberculosis-induced cell death and tissue necrosis. J Exp Med 216 (2019) 556–570. · DOI · Paper page
  24. C.A. Dinarello, Immunological and inflammatory functions of the interleukin-1 family. Annu Rev Immunol 27 (2009) 519–50. · DOI · Paper page
  25. E. Pandur, K. Tamasi, R. Pap, G. Janosa, and K. Sipos, Distinct Effects of Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus Cell Wall Component-Induced Inflammation on the Iron Metabolism of THP-1 Cells. Int J Mol Sci 22 (2021). · DOI
  26. R. Ma, L. Fang, L. Chen, X. Wang, J. Jiang, and L. Gao, Ferroptotic stress promotes macrophages against intracellular bacteria. Theranostics 12 (2022) 2266–2289. · DOI
  27. K.P. Haley, and E.P. Skaar, A battle for iron: host sequestration and Staphylococcus aureus acquisition. Microbes Infect 14 (2012) 217–27. · DOI · Paper page
  28. B.R. Stockwell, Ferroptosis turns 10: Emerging mechanisms, physiological functions, and therapeutic applications. Cell 185 (2022) 2401–2421. · DOI
  29. Y. Ou, S.J. Wang, D. Li, B. Chu, and W. Gu, Activation of SAT1 engages polyamine metabolism with p53-mediated ferroptotic responses. Proc Natl Acad Sci U S A 113 (2016) E6806-E6812.
  30. A.J. Schwartz, N.K. Das, S.K. Ramakrishnan, C. Jain, M.T. Jurkovic, J. Wu, E. Nemeth, S. Lakhal-Littleton, J.A. Colacino, and Y.M. Shah, Hepatic hepcidin/intestinal HIF-2alpha axis maintains iron absorption during iron deficiency and overload. J Clin Invest 129 (2019) 336–348. · DOI · Paper page
  31. W.S. Yang, R. SriRamaratnam, M.E. Welsch, K. Shimada, R. Skouta, V.S. Viswanathan, J.H. Cheah, P.A. Clemons, A.F. Shamji, C.B. Clish, L.M. Brown, A.W. Girotti, V.W. Cornish, S.L. Schreiber, and B.R. Stockwell, Regulation of ferroptotic cancer cell death by GPX4. Cell 156 (2014) 317–331. · DOI · Paper page
  32. S.J. Dixon, K.M. Lemberg, M.R. Lamprecht, R. Skouta, E.M. Zaitsev, C.E. Gleason, D.N. Patel, A.J. Bauer, A.M. Cantley, W.S. Yang, B. Morrison, 3rd, and B.R. Stockwell, Ferroptosis: an iron-dependent form of nonapoptotic cell death. Cell 149 (2012) 1060–72. · DOI · Paper page
  33. L. Yang, H. Wang, X. Yang, Q. Wu, P. An, X. Jin, W. Liu, X. Huang, Y. Li, S. Yan, S. Shen, T. Liang, J. Min, and F. Wang, Auranofin mitigates systemic iron overload and induces ferroptosis via distinct mechanisms. Signal Transduction and Targeted Therapy 5 (2020). · DOI
  34. -. Yingying Yu, * Li Jiang,1,* Hao Wang,3 Zhe Shen,1 Qi Cheng,1 Pan Zhang,1 Jiaming Wang,1 Qian Wu,1 Xuexian Fang,1 Lingyan Duan,1, and K.W. Shufen Wang, 1 Peng An,2 Tuo Shao,4 Raymond T. Chung,4 Shusen Zheng,1 Junxia Min,1 and Fudi Wang1-3, <hepatic transferrin plays a role in systemic iron homeostasis and.pdf>. Blood 136(6):726–739) (2020).
  35. X. Fang, Z. Cai, H. Wang, D. Han, Q. Cheng, P. Zhang, F. Gao, Y. Yu, Z. Song, Q. Wu, P. An, S. Huang, J. Pan, H.-Z. Chen, J. Chen, A. Linkermann, J. Min, and F. Wang, Loss of Cardiac Ferritin H Facilitates Cardiomyopathy via Slc7a11-Mediated Ferroptosis. Circulation Research 127 (2020) 486–501. · DOI
  36. X. Fang, H. Ardehali, J. Min, and F. Wang, The molecular and metabolic landscape of iron and ferroptosis in cardiovascular disease. Nature Reviews Cardiology 20 (2022) 7–23. · DOI
  37. X. Fang, H. Wang, D. Han, E. Xie, X. Yang, J. Wei, S. Gu, F. Gao, N. Zhu, X. Yin, Q. Cheng, P. Zhang, W. Dai, J. Chen, F. Yang, H.T. Yang, A. Linkermann, W. Gu, J. Min, and F. Wang, Ferroptosis as a target for protection against cardiomyopathy. Proc Natl Acad Sci U S A 116 (2019) 2672–2680. · DOI
  38. S. Gao, Y. Gao, L. Cai, and R. Qin, Luteolin attenuates Staphylococcus aureus-induced endometritis through inhibiting ferroptosis and inflammation via activating the Nrf2/GPX4 signaling pathway. Microbiol Spectr (2024) e0327923. · DOI
  39. Y. Du, and Z. Guo, Recent progress in ferroptosis: inducers and inhibitors. Cell Death Discov 8 (2022) 501. · DOI
  40. Y. Huang, W. Xu, and R. Zhou, NLRP3 inflammasome activation and cell death. Cell Mol Immunol 18 (2021) 2114–2127. · DOI · Paper page
  41. L. Zhao, L. Jin, and B. Yang, Diosmetin alleviates S. aureus-induced mastitis by inhibiting SIRT1/GPX4 mediated ferroptosis. Life Sci 331 (2023) 122060. · DOI
  42. M. Qi, H. Geng, N. Geng, Y. Cui, C. Qi, G. Cheng, K. Song, L. Hu, Y. Liu, J. Liu, and B. Han, Streptococcus agalactiae-induced autophagy of bovine mammary epithelial cell via PI3K/AKT/mTOR pathway. Journal of Dairy Research 89 (2022) 178–184. · DOI

Metadata

Authors
jiang, H., yi, J., sun, Z., Li, J., Jiang, Y., Liu, P., Wang, Y., Liu, H., Lv, Q., Kong, D., Huang, W., Ren, Y., & Li, Q.
Affiliations
  • Academy of Military Medical Sciences (CN)
  • Life Science College, Southwest Forestry University
  • Southwest Forestry University (CN)
Corresponding author
  • jiang, Hua
  • Li, Jing
  • Jiang, Yongqiang
Venue
Cell Death Discovery
Published
2024-04-18
Volume
10
Issue
1
Pages
423-423
ISSN
2058-7716 (ISSN-L)
OpenAlex
W4403032921
Cited by
6
References
1
Citations by year
2026: 3 · 2025: 3
FWCI
1.73
Type
journal article
Language
en
Open access
Locations
  • Cell Death Discovery (publishedVersion, cc-by)
  • Research Square (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
State Key Laboratory of Pathogen and Biosecurity
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Ferroptosis and cancer prognosis
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and Maternal Infections
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Keywords
ferroptosis, Streptococcus agalactiae, IL-1β, peritoneal macrophages, lipid peroxidation, host resistance to infection, intra-abdominal infection, innate immunity

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