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Identification of specific Tie2 cleavage sites and therapeutic modulation in experimental sepsis.


ABSTRACT: Endothelial Tie2 signaling plays a pivotal role in vascular barrier maintenance at baseline and after injury. We previously demonstrated that a sharp drop in Tie2 expression observed across various murine models of critical illnesses is associated with increased vascular permeability and mortality. Matrix metalloprotease (MMP)-14-mediated Tie2 ectodomain shedding has recently been recognized as a possible mechanism for Tie2 downregulation in sepsis. Here, we identified the exact MMP14-mediated Tie2 ectodomain cleavage sites and could show that pharmacological MMP14 blockade in experimental murine sepsis exerts barrier protective and anti-inflammatory effects predominantly through the attenuation of Tie2 cleavage to improve survival both in a pre-treatment and rescue approach. Overall, we show that protecting Tie2 shedding might offer a new therapeutic opportunity for the treatment of septic vascular leakage.

SUBMITTER: Idowu TO 

PROVIDER: S-EPMC7447424 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Identification of specific Tie2 cleavage sites and therapeutic modulation in experimental sepsis.

Idowu Temitayo O TO   Etzrodt Valerie V   Seeliger Benjamin B   Bolanos-Palmieri Patricia P   Thamm Kristina K   Haller Hermann H   David Sascha S  

eLife 20200824


Endothelial Tie2 signaling plays a pivotal role in vascular barrier maintenance at baseline and after injury. We previously demonstrated that a sharp drop in Tie2 expression observed across various murine models of critical illnesses is associated with increased vascular permeability and mortality. Matrix metalloprotease (MMP)-14-mediated Tie2 ectodomain shedding has recently been recognized as a possible mechanism for Tie2 downregulation in sepsis. Here, we identified the exact MMP14-mediated T  ...[more]

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