Skip to content
2000
Volume 25, Issue 1
  • ISSN: 1566-5240
  • E-ISSN: 1875-5666

Abstract

Background

Sepsis is a life-threatening disease caused by infection, and developing novel strategies against sepsis is still required. Exosomes derived from mesenchymal stem cells (MSCs) have shown promising therapeutic potential for various diseases. In this study, we aimed to investigate the action and mechanism of exosomes derived from IL-1β-pre-conditioned bone marrow-derived mesenchymal stromal cells (BMSCs) in sepsis.

Methods

Exosomes were isolated from BMSCs that were pretreated with (IL-1β-BMSC/exos) or without IL-1β (BMSC/exos). , a cell model of sepsis was induced by treating human umbilical vein endothelial cells (HUVECs) with lipopolysaccharide (LPS), while , a sepsis model was established through cecal ligation and puncture (CLP) operation. Immunofluorescence staining was used to detect the uptake of exosomes by HUVECs. The effects of exosomes on the cellular function of HUVECs were determined through EDU proliferation assay, migration assay, and tube formation assay. Gene and protein expression were analyzed using qRT-PCR, Western blot, ELISA, immunofluorescence staining, and immuno-histochemistry staining.

Results

IL-1β-BMSC/exos significantly enhanced the proliferation, migration, and tube formation of HUVECs. Treatment with LPS induced the expression of high mobility group box 1 (HMGB1) and the phosphorylation of AKT in HUVECs, but these effects were counteracted by the treatment of IL-1β-BMSC/exos. The protective effect of IL-1β-BMSC/exos on the viability and tube formation ability of HUVECs was reversed by overexpression of HMGB1. Moreover, IL-1β-BMSC/exos promoted the polarization of M2 macrophages and reduced the secretion of inflammatory chemokines. Additionally, IL-1β-BMSC/exos alleviated cecal ligation and puncture (CLP)-induced sepsis .

Conclusion

IL-1β-BMSC/exos alleviates sepsis by modulating the HMGB1/AKT pathway and triggering M2 macrophage polarization.

Loading

Article metrics loading...

/content/journals/cmm/10.2174/0115665240277763231206051401
2024-01-03
2025-01-19
Loading full text...

Full text loading...

References

  1. KellumJ.A. FormeckC.L. KernanK.F. GómezH. CarcilloJ.A. Subtypes and mimics of sepsis.Crit. Care Clin.202238219521110.1016/j.ccc.2021.11.013 35369943
    [Google Scholar]
  2. FernandoS.M. RochwergB. SeelyA.J.E. Clinical implications of the third international consensus definitions for sepsis and septic shock (Sepsis-3).CMAJ201819036E1058E105910.1503/cmaj.170149 30201611
    [Google Scholar]
  3. YaoM. CuiB. ZhangW. MaW. ZhaoG. XingL. Exosomal miR-21 secreted by IL-1β-primed-mesenchymal stem cells induces macrophage M2 polarization and ameliorates sepsis.Life Sci.202126411865810.1016/j.lfs.2020.118658 33115604
    [Google Scholar]
  4. ZhengX. ZhangW. WangZ. Simvastatin preparations promote PDGF‐BB secretion to repair LPS‐induced endothelial injury through the PDGFRβ/PI3K/Akt/IQGAP1 signalling pathway.J. Cell. Mol. Med.201923128314832710.1111/jcmm.14709 31576676
    [Google Scholar]
  5. XiaY. ZhuJ. YangR. WangH. LiY. FuC. Mesenchymal stem cells in the treatment of spinal cord injury: Mechanisms, current advances and future challenges.Front. Immunol.202314114160110.3389/fimmu.2023.1141601 36911700
    [Google Scholar]
  6. MikłoszA. ChabowskiA. Adipose-derived mesenchymal stem cells therapy as a new treatment option for diabetes mellitus.J. Clin. Endocrinol. Metab.202310881889189710.1210/clinem/dgad142 36916961
    [Google Scholar]
  7. KalouY. Al-KhaniA.M. HaiderK.H. Bone marrow mesenchymal stem cells for heart failure treatment: A systematic review and meta-analysis.Heart Lung Circ.202332787088010.1016/j.hlc.2023.01.012 36872163
    [Google Scholar]
  8. LangE. SemonJ.A. Mesenchymal stem cells in the treatment of osteogenesis imperfecta.Cell Regen.2023121710.1186/s13619‑022‑00146‑3 36725748
    [Google Scholar]
  9. LuoC. LuoF. CheL. Mesenchymal stem cells protect against sepsis-associated acute kidney injury by inducing Gal-9/Tim-3 to remodel immune homeostasis.Ren. Fail.2023451218722910.1080/0886022X.2023.2187229 36883358
    [Google Scholar]
  10. XingJ. WangR. CuiF. SongL. MaQ. XuH. Role of the regulation of mesenchymal stem cells on macrophages in sepsis.Int. J. Immunopathol. Pharmacol.20233710.1177/03946320221150722 36840553
    [Google Scholar]
  11. KhosrojerdiA. SoudiS. HosseiniA.Z. EshghiF. ShafieeA. HashemiS.M. Immunomodulatory and therapeutic effects of mesenchymal stem cells on organ dysfunction in sepsis.Shock202155442344010.1097/SHK.0000000000001644 32826813
    [Google Scholar]
  12. PanW. ChenH. WangA. WangF. ZhangX. Challenges and strategies: Scalable and efficient production of mesenchymal stem cells-derived exosomes for cell-free therapy.Life Sci.202331912152410.1016/j.lfs.2023.121524 36828131
    [Google Scholar]
  13. YangE. JingS. WangY. WangH. RodriguezR. WangZ. The role of mesenchymal stem cells and exosomes in tumor development and targeted antitumor therapies.Stem Cells Int.2023202311510.1155/2023/7059289 36824409
    [Google Scholar]
  14. CaoS. HuangY. DaiZ. Circular RNA mmu_circ_0001295 from hypoxia pretreated adipose-derived mesenchymal stem cells (ADSCs) exosomes improves outcomes and inhibits sepsis-induced renal injury in a mouse model of sepsis.Bioengineered20221336323633110.1080/21655979.2022.2044720 35212606
    [Google Scholar]
  15. DengH. ZhuL. ZhangY. Differential lung protective capacity of exosomes derived from human adipose tissue, bone marrow, and umbilical cord mesenchymal stem cells in sepsis-induced acute lung injury.Oxid. Med. Cell. Longev.2022202211510.1155/2022/7837837 35265265
    [Google Scholar]
  16. AnderssonU. YangH. HMGB1 is a critical molecule in the pathogenesis of Gram-negative sepsis.J. Intensive Care20222315616610.1016/j.jointm.2022.02.001 36789020
    [Google Scholar]
  17. IyerS. KennedyJ.N. PowellR. BrantE. Martin-GillC. SeymourC.W. The association between prehospital HMGB1 and sepsis in emergency care.Eur. J. Emerg. Med.2023301525410.1097/MEJ.0000000000000965 36542339
    [Google Scholar]
  18. GuoW. HuZ. SRPK1 promotes sepsis-induced acute lung injury via regulating PI3K/AKT/FOXO3 signaling.Immunopharmacol. Immunotoxicol.202345220321210.1080/08923973.2022.2134789 36226860
    [Google Scholar]
  19. JoffreJ. HellmanJ. InceC. Ait-OufellaH. Endothelial responses in sepsis.Am. J. Respir. Crit. Care Med.2020202336137010.1164/rccm.201910‑1911TR 32101446
    [Google Scholar]
  20. TuF. WangX. ZhangX. Novel role of endothelial derived exosomal HSPA12B in regulating macrophage inflammatory responses in polymicrobial sepsis.Front. Immunol.20201182510.3389/fimmu.2020.00825 32457753
    [Google Scholar]
  21. KongL. LiangM. LiuJ. Mesenchymal stem cell-derived exosomes rescue oxygen-glucose deprivation-induced injury in endothelial cells.Curr. Neurovasc. Res.202017215516310.2174/1567202617666200214103950 32056526
    [Google Scholar]
  22. GongM. YuB. WangJ. Mesenchymal stem cells release exosomes that transfer miRNAs to endothelial cells and promote angiogenesis.Oncotarget2017828452004521210.18632/oncotarget.16778 28423355
    [Google Scholar]
  23. MiL. ZhangY. XuY. HMGB1/RAGE pro-inflammatory axis promotes vascular endothelial cell apoptosis in limb ischemia/reperfusion injury.Biomed. Pharmacother.201911610900510.1016/j.biopha.2019.109005 31136947
    [Google Scholar]
  24. HuangQ. YangZ. ZhouJ.P. LuoY. HMGB1 induces endothelial progenitor cells apoptosis via RAGE-dependent PERK/eIF2α pathway.Mol. Cell. Biochem.20174311-2677410.1007/s11010‑017‑2976‑2 28251435
    [Google Scholar]
  25. ChenG. WardM.F. SamaA.E. WangH. Extracellular HMGB1 as a proinflammatory cytokine.J. Interferon Cytokine Res.200424632933310.1089/107999004323142187 15212706
    [Google Scholar]
  26. ChenK. LiY. ZhangX. UllahR. TongJ. ShenY. The role of the PI3K/AKT signalling pathway in the corneal epithelium: recent updates.Cell Death Dis.202213551310.1038/s41419‑022‑04963‑x 35641491
    [Google Scholar]
  27. AmornsupakK. ThongchotS. ThinyakulC. HMGB1 mediates invasion and PD-L1 expression through RAGE-PI3K/AKT signaling pathway in MDA-MB-231 breast cancer cells.BMC Cancer202222157810.1186/s12885‑022‑09675‑1 35610613
    [Google Scholar]
  28. PuZ. DudaD.G. ZhuY. VCP interaction with HMGB1 promotes hepatocellular carcinoma progression by activating the PI3K/AKT/mTOR pathway.J. Transl. Med.202220121210.1186/s12967‑022‑03416‑5 35562734
    [Google Scholar]
  29. DuX. ZhangX. DongJ. Irradiation-induced exosomal HMGB1 to confer radioresistance via the PI3K/AKT/FOXO3A signaling pathway in ESCC.J. Transl. Med.202220150710.1186/s12967‑022‑03720‑0 36335371
    [Google Scholar]
  30. LiuY.C. ZouX.B. ChaiY.F. YaoY.M. Macrophage polarization in inflammatory diseases.Int. J. Biol. Sci.201410552052910.7150/ijbs.8879 24910531
    [Google Scholar]
  31. ChenX. LiuY. GaoY. ShouS. ChaiY. The roles of macrophage polarization in the host immune response to sepsis.Int. Immunopharmacol.20219610779110.1016/j.intimp.2021.107791 34162154
    [Google Scholar]
  32. Luz-CrawfordP. JorgensenC. DjouadF. Mesenchymal stem cells direct the immunological fate of macrophages.Results Probl. Cell Differ.201762617210.1007/978‑3‑319‑54090‑0_4 28455706
    [Google Scholar]
  33. ArabpourM. SaghazadehA. RezaeiN. Anti-inflammatory and M2 macrophage polarization-promoting effect of mesenchymal stem cell-derived exosomes.Int. Immunopharmacol.20219710782310.1016/j.intimp.2021.107823 34102486
    [Google Scholar]
  34. ZhangJ. RongY. LuoC. CuiW. Bone marrow mesenchymal stem cell-derived exosomes prevent osteoarthritis by regulating synovial macrophage polarization.Aging20201224251382515210.18632/aging.104110 33350983
    [Google Scholar]
/content/journals/cmm/10.2174/0115665240277763231206051401
Loading
/content/journals/cmm/10.2174/0115665240277763231206051401
Loading

Data & Media loading...

Supplements

Supplementary material is available on the publisher's website along with the published article.

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test