Evidence map›Paper›PMID 37126506›Full record

ArticlePloS one2023

A comparison of machine learning approaches for the quantification of microglial cells in the brain of mice, rats and non-human primates.

Danish M Anwer, Francesco Gubinelli, Yunus A Kurt, Livija Sarauskyte, Febe Jacobs, Chiara Venuti, Ivette M Sandoval, Yiyi Yang, Jennifer Stancati, Martina Mazzocchi and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 3 countries.

Danish M AnwerBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Francesco GubinelliBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Yunus A KurtBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Livija SarauskyteBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Febe JacobsBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Chiara VenutiBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Ivette M SandovalBarrow Neurological Institute, Parkinson's Disease Research Unit, Department of Translational Neuroscience, Phoenix, Arizona, United States of America.
Yiyi YangExperimental Neuroinflammation Laboratory, Department of Experimental Medical Sciences, Lund University, Lund, Sweden.
Jennifer StancatiTranslational Neuroscience, College of Human Medicine, Michigan State University, Grand Rapids, MI, United States of America.
Martina MazzocchiBrain Development and Repair Group, Department of Anatomy and Neuroscience University College Cork, Cork, Ireland.
Edoardo BrandiNeural Plasticity and Repair, Department of Experimental Medical Sciences, Lund University, Lund, Sweden.
Gerard O'KeeffeBrain Development and Repair Group, Department of Anatomy and Neuroscience University College Cork, Cork, Ireland.
Kathy Steece-CollierTranslational Neuroscience, College of Human Medicine, Michigan State University, Grand Rapids, MI, United States of America.
Jia-Yi LiNeural Plasticity and Repair, Department of Experimental Medical Sciences, Lund University, Lund, Sweden.
Tomas DeierborgExperimental Neuroinflammation Laboratory, Department of Experimental Medical Sciences, Lund University, Lund, Sweden.
Fredric P ManfredssonBarrow Neurological Institute, Parkinson's Disease Research Unit, Department of Translational Neuroscience, Phoenix, Arizona, United States of America.ORCID 0000-0001-5802-5487
Marcus DavidssonBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.
Andreas HeuerBehavioural Neuroscience Laboratory, Department of Experimental Medical Sciences, Lund University Lund, Sweden.ORCID 0000-0003-0300-7606
Lund University · SEBarrow Neurological Institute · USMichigan State University · USUniversity College Cork · IE

Funding

Genetic Silencing of Striatal CaV1.3 Calcium Channels as a Potent Antidyskinetic Therapy for PDR01NS110398 · NINDS · MICHIGAN STATE UNIVERSITY · PI Jeffrey H Kordower, Fredric Manfredsson · 2018 to 2026
$5.3M
Gut-Brain Axis in Alzheimer's DiseaseR01DK108798 · NIDDK · ST. JOSEPH'S HOSPITAL AND MEDICAL CENTER · PI MANFREDSSON, FREDRIC · 2017 to 2021
$2.1M
Impact of Dysfunctional BDNF on Dopamine Terminal Remodeling in the Parkinsonian StriatumR01NS105826 · NINDS · MICHIGAN STATE UNIVERSITY · PI STEECE-COLLIER, KATHY · 2019 to 2023
$1.8M
The Rat Pre-Formed Alpha-Synuclein Fibril Model of Parkinson's DiseaseR33NS099416 · NINDS · MICHIGAN STATE UNIVERSITY · PI SORTWELL, CARYL E · 2018 to 2019
$899k
The Rat Pre-Formed Alpha-Synuclein Fibril Model of Parkinson's DiseaseR21NS099416 · NINDS · MICHIGAN STATE UNIVERSITY · PI SORTWELL, CARYL E · 2017 to 2017
$398k
NIDDK NIH HHS R01 DK108798NINDS NIH HHS R01 NS105826NINDS NIH HHS R01 NS110398NINDS NIH HHS R21 NS099416NINDS NIH HHS R33 NS099416
6 · The paper itself

Abstract

Microglial cells are brain-specific macrophages that swiftly react to disruptive events in the brain. Microglial activation leads to specific modifications, including proliferation, morphological changes, migration to the site of insult, and changes in gene expression profiles. A change in inflammatory status has been linked to many neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease. For this reason, the investigation and quantification of microglial cells is essential for better understanding their role in disease progression as well as for evaluating the cytocompatibility of novel therapeutic approaches for such conditions. In the following study we implemented a machine learning-based approach for the fast and automatized quantification of microglial cells; this tool was compared with manual quantification (ground truth), and with alternative free-ware such as the threshold-based ImageJ and the machine learning-based Ilastik. We first trained the algorithms on brain tissue obtained from rats and non-human primate immunohistochemically labelled for microglia. Subsequently we validated the accuracy of the trained algorithms in a preclinical rodent model of Parkinson's disease and demonstrated the robustness of the algorithms on tissue obtained from mice, as well as from images provided by three collaborating laboratories. Our results indicate that machine learning algorithms can detect and quantify microglial cells in all the three mammalian species in a precise manner, equipotent to the one observed following manual counting. Using this tool, we were able to detect and quantify small changes between the hemispheres, suggesting the power and reliability of the algorithm. Such a tool will be very useful for investigation of microglial response in disease development, as well as in the investigation of compatible novel therapeutics targeting the brain. As all network weights and labelled training data are made available, together with our step-by-step user guide, we anticipate that many laboratories will implement machine learning-based quantification of microglial cells in their research.

Indexed as

MicrogliaParkinson DiseaseAnimalsBrainMachine LearningMammalsMicePrimatesRatsReproducibility of Results

Identifiers

PMID37126506
PMCPMC10150977
OpenAlexW4367597984

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.