ProNGF processing in adult rat tissues and bioactivity of NGF prodomain peptides

Author:

Makoudjou Marie Anne12,Fico Elena2,Rosso Pamela2,Triaca Viviana3,De Simone Lucio4,Rossetti Daniela4,Cattani Franca4,Allegretti Marcello4,Tirassa Paola2ORCID

Affiliation:

1. Cellular and Molecular Biology, Department of Biology University of Rome “Tor Vergata” Rome Italy

2. Institute of Biochemistry and Cell Biology (IBBC) National Research Council (CNR) Rome Italy

3. Institute of Biochemistry and Cell Biology (IBBC) National Research Council (CNR) Campus A. Buzzati‐Traverso, Monterotondo Rome Italy

4. Dompé Farmaceutici S.p.A L'Aquila Italy

Abstract

The neurotrophin nerve growth factor (NGF) and its precursor proNGF are both bioactive and exert similar or opposite actions depending on the cell target and its milieu. The balance between NGF and proNGF is crucial for cell and tissue homeostasis and it is considered an indicator of pathological conditions. Proteolytical cleavage of proNGF to the mature form results in different fragments, whose function and/or bioactivity is still unclear. The present study was conducted to investigate the distribution of proNGF fragments derived from endogenous cleavage in brain and peripheral tissues of adult rats in the healthy condition and following inflammatory lipopolysaccharide (LPS) challenge. Different anti‐proNGF antibodies were tested and the presence of short peptides corresponding to the prodomain sequence (pdNGFpep) was identified. Processing of proNGF was found to be tissue‐specific and accumulation of pdNGFpeps was found in inflamed tissues, mainly in testis, intestine and heart, suggesting a possible correlation between organ functions and a response to insults and/or injury. The bioactivity of pdNGFpep was also demonstrated in vitro by using primary hippocampal neurons. Our study supports a biological function for the NGF precursor prodomain and indicates that short peptides from residues 1–60, differing from the 70–110 sequence, induce apoptosis, thereby opening the way for identification of new molecular targets to study pathological conditions.

Publisher

Wiley

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