Abstract

Plasminogen activation is involved in many processes within the central nervous system, including synaptic plasticity, neuroinflammation and neurodegeneration. However, the mechanisms that regulate plasminogen activation in the brain still remain unknown. Here we demonstrate that astrocytes participate in this regulation by two mechanisms. First, the astrocyte plasma membrane serves as a surface for plasminogen activation by tissue-type plasminogen activator. This activation triggers downstream plasmin-dependent processes with important impacts in brain health and disease, such as fibrinolysis and brain-derived neurotrophic factor conversion. Second, astrocytes take up plasminogen and plasmin in a regulated manner through a novel mechanism involving endocytosis mediated by cell-surface actin and triggered by extracellular plasmin activity at the surface of astrocytes. Following endocytosis, plasminogen and plasmin are targeted to lysosomes for degradation. Thus, cell-surface actin acts as a sensor of plasmin activity to induce a negative feedback through plasmin endocytosis. This study provides evidence that astrocytes control the balance between plasmin formation and plasmin elimination in the brain parenchyma.

Highlights

  • Plasminogen activation system refers to the enzymatic processes leading to regulated activation of the zymogen plasminogen into the broad-spectrum serine protease plasmin

  • We compared the effect of astrocytes on plasminogen activation mediated by tissueplasminogen activator (tPA) and urokinase-type plasminogen activator

  • We observed that plasmin formation was enhanced by astrocytes only when plasminogen was incubated with tPA but not when incubated with urokinase-type plasminogen activator (uPA) (Figure 1b)

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Summary

Introduction

Plasminogen activation system refers to the enzymatic processes leading to regulated activation of the zymogen plasminogen into the broad-spectrum serine protease plasmin. This system was initially described in the vasculature, where it regulates fibrinolysis (the degradation of fibrin clots). Once plasmin is generated, due to its wide range of action, regulatory mechanisms are required to restrict its activity to a very close spatiotemporal window. This is why the issue of cerebral plasmin clearance systems needs to be addressed

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