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IL-6 trans-Signaling Impairs Sprouting Angiogenesis by Inhibiting Migration, Proliferation and Tube Formation of Human Endothelial Cells

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  • معلومة اضافية
    • بيانات النشر:
      Linköpings universitet, Avdelningen för inflammation och infektion
      Linköpings universitet, Medicinska fakulteten
      Orebro Univ, Sweden
    • الموضوع:
      2020
    • Collection:
      Linköping University Electronic Press (LiU E-Press)
    • نبذة مختصرة :
      Sprouting angiogenesis is the formation of new capillaries from existing vessels in response to tissue hypoxia due to growth/development, repair/healing, and also chronic inflammation. In this study, we aimed to elucidate the effect of IL-6, a pleiotropic cytokine with both pro-inflammatory and anti-inflammatory functions, in regulating the sprouting angiogenic response of endothelial cells (ECs). We found that activation of IL-6 trans-signaling inhibited the migration, proliferation, and tube formation ability of ECs. In addition, inhibition of the autocrine IL-6 classic-signaling by depleting endogenous IL-6 from ECs impaired their tube formation ability. At the molecular level, we found that IL-6 trans-signaling in ECs upregulated established endogenous anti-angiogenic factors such asCXCL10andSERPINF1while at the same time downregulated known endogenous pro-angiogenic factors such ascKITandCXCL8. Furthermore, prior activation of ECs by IL-6 trans-signaling alters their response to vascular endothelial growth factor-A (VEGF-A), causing an increased p38, but decreased Erk1/2 phosphorylation. Collectively, our data demonstrated the dual facets of IL-6 in regulating the sprouting angiogenic function of ECs. In addition, we shed light on molecular mechanisms behind the IL-6 trans-signaling mediated impairment of endothelial sprouting angiogenic response. ; Funding Agencies|Stiftelsen for Kunskaps-och Kompetensutveckling [Dnr20180035]; Orebro University
    • File Description:
      application/pdf
    • Relation:
      Cells, 2020, 9:6; orcid:0000-0002-9562-0872; http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-168308; PMID 32517159; ISI:000550752000001; Scopus 2-s2.0-85086354593
    • الرقم المعرف:
      10.3390/cells9061414
    • الدخول الالكتروني :
      http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-168308
      https://doi.org/10.3390/cells9061414
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.C8722FB9