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A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing

This paper reports on a novel application of an amphoteric water-soluble polyamidoamine named AGMA1 bearing 4-butylguanidine pendants. AGMA1 is an amphoteric, prevailingly cationic polyelectrolyte with isoelectric point of about 10. At pH 7.4 it is zwitterionic with an average of 0.55 excess positiv...

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Autores principales: Tonna, Noemi, Bianco, Fabio, Matteoli, Michela, Cagnoli, Cinzia, Antonucci, Flavia, Manfredi, Amedea, Mauro, Nicolò, Ranucci, Elisabetta, Ferruti, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090696/
https://www.ncbi.nlm.nih.gov/pubmed/27877708
http://dx.doi.org/10.1088/1468-6996/15/4/045007
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author Tonna, Noemi
Bianco, Fabio
Matteoli, Michela
Cagnoli, Cinzia
Antonucci, Flavia
Manfredi, Amedea
Mauro, Nicolò
Ranucci, Elisabetta
Ferruti, Paolo
author_facet Tonna, Noemi
Bianco, Fabio
Matteoli, Michela
Cagnoli, Cinzia
Antonucci, Flavia
Manfredi, Amedea
Mauro, Nicolò
Ranucci, Elisabetta
Ferruti, Paolo
author_sort Tonna, Noemi
collection PubMed
description This paper reports on a novel application of an amphoteric water-soluble polyamidoamine named AGMA1 bearing 4-butylguanidine pendants. AGMA1 is an amphoteric, prevailingly cationic polyelectrolyte with isoelectric point of about 10. At pH 7.4 it is zwitterionic with an average of 0.55 excess positive charges per unit, notwithstanding it is highly biocompatible. In this work, it was found that AGMA1 surface-adsorbed on cell culturing coverslips exhibits excellent properties as adhesion and proliferation promoter of primary brain cells such as microglia, as well as of hippocampal neurons and astrocytes. Microglia cells cultured on AGMA1-coated coverslips substrate displayed the typical resting, ramified morphology of those cultured on poly-L-lysine and poly-L-ornithine, employed as reference substrates. Mixed cultures of primary astrocytes and neuronal cells grown on AGMA1- and poly-L-lysine coated coverslips were morphologically undistinguishable. On both substrates, neurons differentiated axon and dendrites and eventually established perfectly functional synaptic contacts. Quantitative immunocytochemical staining revealed no difference between AGMA1 and poly-L-lysine. Electrophysiological experiments allowed recording neuron spontaneous activity on AGMA1. In addition, cell cultures on both AGMA1 and PLL displayed comparable excitatory and inhibitory neurotransmission, demonstrating that the synaptic contacts formed were fully functional.
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spelling pubmed-50906962016-11-22 A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing Tonna, Noemi Bianco, Fabio Matteoli, Michela Cagnoli, Cinzia Antonucci, Flavia Manfredi, Amedea Mauro, Nicolò Ranucci, Elisabetta Ferruti, Paolo Sci Technol Adv Mater Papers This paper reports on a novel application of an amphoteric water-soluble polyamidoamine named AGMA1 bearing 4-butylguanidine pendants. AGMA1 is an amphoteric, prevailingly cationic polyelectrolyte with isoelectric point of about 10. At pH 7.4 it is zwitterionic with an average of 0.55 excess positive charges per unit, notwithstanding it is highly biocompatible. In this work, it was found that AGMA1 surface-adsorbed on cell culturing coverslips exhibits excellent properties as adhesion and proliferation promoter of primary brain cells such as microglia, as well as of hippocampal neurons and astrocytes. Microglia cells cultured on AGMA1-coated coverslips substrate displayed the typical resting, ramified morphology of those cultured on poly-L-lysine and poly-L-ornithine, employed as reference substrates. Mixed cultures of primary astrocytes and neuronal cells grown on AGMA1- and poly-L-lysine coated coverslips were morphologically undistinguishable. On both substrates, neurons differentiated axon and dendrites and eventually established perfectly functional synaptic contacts. Quantitative immunocytochemical staining revealed no difference between AGMA1 and poly-L-lysine. Electrophysiological experiments allowed recording neuron spontaneous activity on AGMA1. In addition, cell cultures on both AGMA1 and PLL displayed comparable excitatory and inhibitory neurotransmission, demonstrating that the synaptic contacts formed were fully functional. Taylor & Francis 2014-08-20 /pmc/articles/PMC5090696/ /pubmed/27877708 http://dx.doi.org/10.1088/1468-6996/15/4/045007 Text en © 2014 National Institute for Materials Science http://creativecommons.org/licenses/by/3.0/ Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence (http://creativecommons.org/licenses/by/3.0) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.
spellingShingle Papers
Tonna, Noemi
Bianco, Fabio
Matteoli, Michela
Cagnoli, Cinzia
Antonucci, Flavia
Manfredi, Amedea
Mauro, Nicolò
Ranucci, Elisabetta
Ferruti, Paolo
A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title_full A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title_fullStr A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title_full_unstemmed A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title_short A soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
title_sort soluble biocompatible guanidine-containing polyamidoamine as promoter of primary brain cell adhesion and in vitro cell culturing
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5090696/
https://www.ncbi.nlm.nih.gov/pubmed/27877708
http://dx.doi.org/10.1088/1468-6996/15/4/045007
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