Neuronal conversion of single-chain tissue-type plasminogen activator into its two-chain form: implications in neurodevelopment, learning, and memory

TL;DR

This paper shows how neurons convert a single-chain form of tPA into a two-chain form, which may influence brain development and memory.

Contribution

The study identifies neurons as the primary cells responsible for converting single-chain tPA into two-chain tPA in the brain.

Findings

Neurons are the main brain cells that cleave single-chain tPA into two-chain tPA.

The conversion process involves plasminogen binding, activation into plasmin, and subsequent cleavage of tPA.

The cleavage mechanism depends on the Kringle 2 domain of tPA and is independent of plasminogen LBS.

Abstract

Tissue-type plasminogen activator (tPA) is a serine protease expressed in the central nervous system (CNS) that exhibits various effects, from neurodevelopment to learning and memory processes. tPA is secreted in its single-chain form (sc-tPA) and can be cleaved into a two-chain form (tc-tPA), with the two isoforms displaying sometimes opposite effects within the CNS. Using Alexa Fluor-conjugated recombinant tPA and complementary pharmacological approaches, we evaluated the ability of brain cells to process sc- into tc-tPA and the mechanisms involved. Our data revealed that neurons are the main brain cells capable to cleave sc-tPA into tc-tPA. This process occurs in three steps: 1) plasminogen binds to the cell surface of cortical neurons; 2) sc-tPA activates plasminogen into plasmin; 3) the generated plasmin cleaves sc-tPA into tc-tPA. The cleavage of tPA requires its Kringle 2 domain and is independent of plasminogen LBS. This cleavage mechanism represents a new modulation of tPA’s functions within the CNS.

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