Cargando…

Melanoma Cells Homing to the Brain: An In Vitro Model

We developed an in vitro contact through-feet blood brain barrier (BBB) model built using type IV collagen, rat astrocytes, and human umbilical vein endothelial cells (HUVECs) cocultured through Transwell porous polycarbonate membrane. The contact between astrocytes and HUVECs was demonstrated by el...

Descripción completa

Detalles Bibliográficos
Autores principales: Rizzo, A., Vasco, C., Girgenti, V., Fugnanesi, V., Calatozzolo, C., Canazza, A., Salmaggi, A., Rivoltini, L., Morbin, M., Ciusani, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321090/
https://www.ncbi.nlm.nih.gov/pubmed/25692137
http://dx.doi.org/10.1155/2015/476069
_version_ 1782356232438284288
author Rizzo, A.
Vasco, C.
Girgenti, V.
Fugnanesi, V.
Calatozzolo, C.
Canazza, A.
Salmaggi, A.
Rivoltini, L.
Morbin, M.
Ciusani, E.
author_facet Rizzo, A.
Vasco, C.
Girgenti, V.
Fugnanesi, V.
Calatozzolo, C.
Canazza, A.
Salmaggi, A.
Rivoltini, L.
Morbin, M.
Ciusani, E.
author_sort Rizzo, A.
collection PubMed
description We developed an in vitro contact through-feet blood brain barrier (BBB) model built using type IV collagen, rat astrocytes, and human umbilical vein endothelial cells (HUVECs) cocultured through Transwell porous polycarbonate membrane. The contact between astrocytes and HUVECs was demonstrated by electron microscopy: astrocytes endfeet pass through the 8.0 μm pores inducing HUVECs to assume a cerebral phenotype. Using this model we evaluated transmigration of melanoma cells from two different patients (M1 and M2) selected among seven melanoma primary cultures. M2 cells showed a statistically significant higher capability to pass across the in vitro BBB model, compared to M1. Expression of adhesion molecules was evaluated by flow cytometry: a statistically significant increased expression of MCAM, αvβ3, and CD49b was detected in M1. PCR array data showed that M2 had a higher expression of several matrix metalloproteinase proteins (MMPs) compared to M1. Specifically, data suggest that MMP2 and MMP9 could be directly involved in BBB permeability and that brain invasion by melanoma cells could be related to the overexpression of many MMPs. Future studies will be necessary to deepen the mechanisms of central nervous system invasion.
format Online
Article
Text
id pubmed-4321090
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-43210902015-02-17 Melanoma Cells Homing to the Brain: An In Vitro Model Rizzo, A. Vasco, C. Girgenti, V. Fugnanesi, V. Calatozzolo, C. Canazza, A. Salmaggi, A. Rivoltini, L. Morbin, M. Ciusani, E. Biomed Res Int Research Article We developed an in vitro contact through-feet blood brain barrier (BBB) model built using type IV collagen, rat astrocytes, and human umbilical vein endothelial cells (HUVECs) cocultured through Transwell porous polycarbonate membrane. The contact between astrocytes and HUVECs was demonstrated by electron microscopy: astrocytes endfeet pass through the 8.0 μm pores inducing HUVECs to assume a cerebral phenotype. Using this model we evaluated transmigration of melanoma cells from two different patients (M1 and M2) selected among seven melanoma primary cultures. M2 cells showed a statistically significant higher capability to pass across the in vitro BBB model, compared to M1. Expression of adhesion molecules was evaluated by flow cytometry: a statistically significant increased expression of MCAM, αvβ3, and CD49b was detected in M1. PCR array data showed that M2 had a higher expression of several matrix metalloproteinase proteins (MMPs) compared to M1. Specifically, data suggest that MMP2 and MMP9 could be directly involved in BBB permeability and that brain invasion by melanoma cells could be related to the overexpression of many MMPs. Future studies will be necessary to deepen the mechanisms of central nervous system invasion. Hindawi Publishing Corporation 2015 2015-01-26 /pmc/articles/PMC4321090/ /pubmed/25692137 http://dx.doi.org/10.1155/2015/476069 Text en Copyright © 2015 A. Rizzo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rizzo, A.
Vasco, C.
Girgenti, V.
Fugnanesi, V.
Calatozzolo, C.
Canazza, A.
Salmaggi, A.
Rivoltini, L.
Morbin, M.
Ciusani, E.
Melanoma Cells Homing to the Brain: An In Vitro Model
title Melanoma Cells Homing to the Brain: An In Vitro Model
title_full Melanoma Cells Homing to the Brain: An In Vitro Model
title_fullStr Melanoma Cells Homing to the Brain: An In Vitro Model
title_full_unstemmed Melanoma Cells Homing to the Brain: An In Vitro Model
title_short Melanoma Cells Homing to the Brain: An In Vitro Model
title_sort melanoma cells homing to the brain: an in vitro model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321090/
https://www.ncbi.nlm.nih.gov/pubmed/25692137
http://dx.doi.org/10.1155/2015/476069
work_keys_str_mv AT rizzoa melanomacellshomingtothebrainaninvitromodel
AT vascoc melanomacellshomingtothebrainaninvitromodel
AT girgentiv melanomacellshomingtothebrainaninvitromodel
AT fugnanesiv melanomacellshomingtothebrainaninvitromodel
AT calatozzoloc melanomacellshomingtothebrainaninvitromodel
AT canazzaa melanomacellshomingtothebrainaninvitromodel
AT salmaggia melanomacellshomingtothebrainaninvitromodel
AT rivoltinil melanomacellshomingtothebrainaninvitromodel
AT morbinm melanomacellshomingtothebrainaninvitromodel
AT ciusanie melanomacellshomingtothebrainaninvitromodel