Cargando…

Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis

It is known that microglia morphology and function are closely related, but only few studies have objectively described different morphological subtypes. To address this issue, morphological parameters of microglial cells were analyzed in a rat model of aseptic neuroinflammation. After the injection...

Descripción completa

Detalles Bibliográficos
Autores principales: Fernández-Arjona, María del Mar, Grondona, Jesús M., Granados-Durán, Pablo, Fernández-Llebrez, Pedro, López-Ávalos, María D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550745/
https://www.ncbi.nlm.nih.gov/pubmed/28848398
http://dx.doi.org/10.3389/fncel.2017.00235
_version_ 1783256176435134464
author Fernández-Arjona, María del Mar
Grondona, Jesús M.
Granados-Durán, Pablo
Fernández-Llebrez, Pedro
López-Ávalos, María D.
author_facet Fernández-Arjona, María del Mar
Grondona, Jesús M.
Granados-Durán, Pablo
Fernández-Llebrez, Pedro
López-Ávalos, María D.
author_sort Fernández-Arjona, María del Mar
collection PubMed
description It is known that microglia morphology and function are closely related, but only few studies have objectively described different morphological subtypes. To address this issue, morphological parameters of microglial cells were analyzed in a rat model of aseptic neuroinflammation. After the injection of a single dose of the enzyme neuraminidase (NA) within the lateral ventricle (LV) an acute inflammatory process occurs. Sections from NA-injected animals and sham controls were immunolabeled with the microglial marker IBA1, which highlights ramifications and features of the cell shape. Using images obtained by section scanning, individual microglial cells were sampled from various regions (septofimbrial nucleus, hippocampus and hypothalamus) at different times post-injection (2, 4 and 12 h). Each cell yielded a set of 15 morphological parameters by means of image analysis software. Five initial parameters (including fractal measures) were statistically different in cells from NA-injected rats (most of them IL-1β positive, i.e., M1-state) compared to those from control animals (none of them IL-1β positive, i.e., surveillant state). However, additional multimodal parameters were revealed more suitable for hierarchical cluster analysis (HCA). This method pointed out the classification of microglia population in four clusters. Furthermore, a linear discriminant analysis (LDA) suggested three specific parameters to objectively classify any microglia by a decision tree. In addition, a principal components analysis (PCA) revealed two extra valuable variables that allowed to further classifying microglia in a total of eight sub-clusters or types. The spatio-temporal distribution of these different morphotypes in our rat inflammation model allowed to relate specific morphotypes with microglial activation status and brain location. An objective method for microglia classification based on morphological parameters is proposed. Main points: Microglia undergo a quantifiable morphological change upon neuraminidase induced inflammation. Hierarchical cluster and principal components analysis allow morphological classification of microglia. Brain location of microglia is a relevant factor.
format Online
Article
Text
id pubmed-5550745
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-55507452017-08-28 Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis Fernández-Arjona, María del Mar Grondona, Jesús M. Granados-Durán, Pablo Fernández-Llebrez, Pedro López-Ávalos, María D. Front Cell Neurosci Neuroscience It is known that microglia morphology and function are closely related, but only few studies have objectively described different morphological subtypes. To address this issue, morphological parameters of microglial cells were analyzed in a rat model of aseptic neuroinflammation. After the injection of a single dose of the enzyme neuraminidase (NA) within the lateral ventricle (LV) an acute inflammatory process occurs. Sections from NA-injected animals and sham controls were immunolabeled with the microglial marker IBA1, which highlights ramifications and features of the cell shape. Using images obtained by section scanning, individual microglial cells were sampled from various regions (septofimbrial nucleus, hippocampus and hypothalamus) at different times post-injection (2, 4 and 12 h). Each cell yielded a set of 15 morphological parameters by means of image analysis software. Five initial parameters (including fractal measures) were statistically different in cells from NA-injected rats (most of them IL-1β positive, i.e., M1-state) compared to those from control animals (none of them IL-1β positive, i.e., surveillant state). However, additional multimodal parameters were revealed more suitable for hierarchical cluster analysis (HCA). This method pointed out the classification of microglia population in four clusters. Furthermore, a linear discriminant analysis (LDA) suggested three specific parameters to objectively classify any microglia by a decision tree. In addition, a principal components analysis (PCA) revealed two extra valuable variables that allowed to further classifying microglia in a total of eight sub-clusters or types. The spatio-temporal distribution of these different morphotypes in our rat inflammation model allowed to relate specific morphotypes with microglial activation status and brain location. An objective method for microglia classification based on morphological parameters is proposed. Main points: Microglia undergo a quantifiable morphological change upon neuraminidase induced inflammation. Hierarchical cluster and principal components analysis allow morphological classification of microglia. Brain location of microglia is a relevant factor. Frontiers Media S.A. 2017-08-08 /pmc/articles/PMC5550745/ /pubmed/28848398 http://dx.doi.org/10.3389/fncel.2017.00235 Text en Copyright © 2017 Fernández-Arjona, Grondona, Granados-Durán, Fernández-Llebrez and López-Ávalos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Fernández-Arjona, María del Mar
Grondona, Jesús M.
Granados-Durán, Pablo
Fernández-Llebrez, Pedro
López-Ávalos, María D.
Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title_full Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title_fullStr Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title_full_unstemmed Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title_short Microglia Morphological Categorization in a Rat Model of Neuroinflammation by Hierarchical Cluster and Principal Components Analysis
title_sort microglia morphological categorization in a rat model of neuroinflammation by hierarchical cluster and principal components analysis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550745/
https://www.ncbi.nlm.nih.gov/pubmed/28848398
http://dx.doi.org/10.3389/fncel.2017.00235
work_keys_str_mv AT fernandezarjonamariadelmar microgliamorphologicalcategorizationinaratmodelofneuroinflammationbyhierarchicalclusterandprincipalcomponentsanalysis
AT grondonajesusm microgliamorphologicalcategorizationinaratmodelofneuroinflammationbyhierarchicalclusterandprincipalcomponentsanalysis
AT granadosduranpablo microgliamorphologicalcategorizationinaratmodelofneuroinflammationbyhierarchicalclusterandprincipalcomponentsanalysis
AT fernandezllebrezpedro microgliamorphologicalcategorizationinaratmodelofneuroinflammationbyhierarchicalclusterandprincipalcomponentsanalysis
AT lopezavalosmariad microgliamorphologicalcategorizationinaratmodelofneuroinflammationbyhierarchicalclusterandprincipalcomponentsanalysis