» Articles » PMID: 36873154

Novel Image Analysis Tool for Rapid Screening of Cell Morphology in Preclinical Animal Models of Disease

Overview
Journal Heliyon
Specialty Social Sciences
Date 2023 Mar 6
PMID 36873154
Authors
Affiliations
Soon will be listed here.
Abstract

The field of cell biology has seen major advances in both cellular imaging modalities and the development of automated image analysis platforms that increase rigor, reproducibility, and throughput for large imaging data sets. However, there remains a need for tools that provide accurate morphometric analysis of single cells with complex, dynamic cytoarchitecture in a high-throughput and unbiased manner. We developed a fully automated image-analysis algorithm to rapidly detect and quantify changes in cellular morphology using microglia cells, an innate immune cell within the central nervous system, as representative of cells that exhibit dynamic and complex cytoarchitectural changes. We used two preclinical animal models that exhibit robust changes in microglia morphology: (1) a rat model of acute organophosphate intoxication, which was used to generate fluorescently labeled images for algorithm development; and (2) a rat model of traumatic brain injury, which was used to validate the algorithm using cells labeled using chromogenic detection methods. All brain sections were immunolabeled for IBA-1 using fluorescence or diaminobenzidine (DAB) labeling, images were acquired using a high content imaging system and analyzed using a custom-built algorithm. The exploratory data set revealed eight statistically significant and quantitative morphometric parameters that distinguished between phenotypically distinct groups of microglia. Manual validation of single-cell morphology was strongly correlated with the automated analysis and was further supported by a comparison with traditional stereology methods. Existing image analysis pipelines rely on high-resolution images of individual cells, which limits sample size and is subject to selection bias. However, our fully automated method integrates quantification of morphology and fluorescent/chromogenic signals in images from multiple brain regions acquired using high-content imaging. In summary, our free, customizable image analysis tool provides a high-throughput, unbiased method for accurately detecting and quantifying morphological changes in cells with complex morphologies.

Citing Articles

Glial reactivity and T cell infiltration in frontotemporal lobar degeneration with tau pathology.

Hartnell I, Woodhouse D, Jasper W, Mason L, Marwaha P, Graffeuil M Brain. 2023; 147(2):590-606.

PMID: 37703311 PMC: 10834257. DOI: 10.1093/brain/awad309.

References
1.
Basilico B, Cortese B, Ratano P, Di Angelantonio S, Ragozzino D . Time-lapse Whole-field Fluorescence Imaging of Microglia ProcessesMotility in Acute Mouse Hippocampal Slices and Analysis. Bio Protoc. 2021; 9(8):e3220. PMC: 7854105. DOI: 10.21769/BioProtoc.3220. View

2.
Kreutzberg G . Microglia: a sensor for pathological events in the CNS. Trends Neurosci. 1996; 19(8):312-8. DOI: 10.1016/0166-2236(96)10049-7. View

3.
Saraiva B, Krippahl L, Filipe S, Henriques R, Pinho M . eHooke: A tool for automated image analysis of spherical bacteria based on cell cycle progression. Biol Imaging. 2022; 1:e3. PMC: 8724265. DOI: 10.1017/S2633903X21000027. View

4.
Chiocchetti A, Tolosano E, Hirsch E, Silengo L, Altruda F . Green fluorescent protein as a reporter of gene expression in transgenic mice. Biochim Biophys Acta. 1997; 1352(2):193-202. DOI: 10.1016/s0167-4781(97)00010-9. View

5.
Guignet M, Dhakal K, Flannery B, Hobson B, Zolkowska D, Dhir A . Persistent behavior deficits, neuroinflammation, and oxidative stress in a rat model of acute organophosphate intoxication. Neurobiol Dis. 2019; 133:104431. PMC: 6754818. DOI: 10.1016/j.nbd.2019.03.019. View