Journal Article

Bv8/prokineticin 2 is involved in Aβ-induced neurotoxicity

Lattanzi, Roberta, Florenzano, Fulvio, Zona, Cristina, Maftei, Daniela, Severini, Cinzia, Ciotti, Maria Teresa, Balboni, Gianfranco, Caioli, Silvia, Nisticò, Robert, Marconi, Veronica, Del Duca, Ester, Negri, Lucia, Petrocchi Passeri, Pamela, Salvadori, Severo

2015

Overview

Bv8/Prokineticin 2 (PROK2) is a bioactive peptide initially discovered as a regulator of gastrointestinal motility. Among multiple biological roles demonstrated for PROK2, it was recently established that PROK2 is an insult-inducible endangering mediator for cerebral damage. Aim of the present study was to evaluate the PROK2 and its receptors’ potential involvement in amyloid beta (Aβ) neurotoxicity, a hallmark of Alzheimer’s disease (AD) and various forms of traumatic brain injury (TBI). Analyzing primary cortical cultures (CNs) and cortex and hippocampus from Aβ treated rats, we found that PROK2 and its receptors PKR 1 and PKR 2 mRNA are up-regulated by Aβ, suggesting their potential involvement in AD. Hence we evaluated if impairing the prokineticin system activation might have protective effect against neuronal death induced by Aβ. We found that a PKR antagonist concentration-dependently protects CNs against Aβ 1–42 -induced neurotoxicity, by reducing the Aβ-induced PROK2 neuronal up-regulation. Moreover, the antagonist completely rescued LTP impairment in hippocampal slices from 6 month-old Tg2576 AD mice without affecting basal synaptic transmission and paired pulse-facilitation paradigms. These results indicate that PROK2 plays a role in cerebral amyloidosis and that PROK2 antagonists may represent a new approach for ameliorating the defining pathology of AD.

• Publisher: Nature Publishing Group UK
• Subject: 13 / 13/1 / 13/2 / 13/21 / 13/51 / 14 / 14/19 / 38 / 38/77 / 631/378/1689/1283 / 64 / 64/110 / 692/308/1426 / 96/106 / Alzheimer Disease - genetics / Alzheimer Disease - metabolism / Amyloid beta-Peptides - metabolism / Amyloid beta-Peptides - toxicity / Animals / Apoptosis - drug effects / Gastrointestinal Hormones - genetics / Gastrointestinal Hormones - metabolism / Gene Expression Regulation - drug effects / Hippocampus - metabolism / Humanities and Social Sciences / Long-Term Potentiation - drug effects / Long-Term Potentiation - genetics / Male / Mice / Mice, Transgenic / multidisciplinary / Neurons - drug effects / Neurons - metabolism / Neuropeptides - genetics / Neuropeptides - metabolism / Peptide Fragments - metabolism / Peptide Fragments - toxicity / Protein Transport / Rats / Receptors, G-Protein-Coupled - antagonists & inhibitors / Receptors, G-Protein-Coupled - genetics / Receptors, G-Protein-Coupled - metabolism / Science / Up-Regulation