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The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER

New histological techniques are needed to examine protein distribution in human tissues, which can reveal cell shape and disease pathology connections. Spatial proteomics has changed the study of tumor microenvironments by identifying spatial relationships of immunomodulatory cells and proteins and...

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Autores principales: Shahidehpour, Ryan K., Nelson, Abraham S., Sanders, Lydia G., Embry, Chloe R., Nelson, Peter T., Bachstetter, Adam D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024857/
https://www.ncbi.nlm.nih.gov/pubmed/36934255
http://dx.doi.org/10.1186/s40478-023-01541-w
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author Shahidehpour, Ryan K.
Nelson, Abraham S.
Sanders, Lydia G.
Embry, Chloe R.
Nelson, Peter T.
Bachstetter, Adam D.
author_facet Shahidehpour, Ryan K.
Nelson, Abraham S.
Sanders, Lydia G.
Embry, Chloe R.
Nelson, Peter T.
Bachstetter, Adam D.
author_sort Shahidehpour, Ryan K.
collection PubMed
description New histological techniques are needed to examine protein distribution in human tissues, which can reveal cell shape and disease pathology connections. Spatial proteomics has changed the study of tumor microenvironments by identifying spatial relationships of immunomodulatory cells and proteins and contributing to the discovery of new cancer immunotherapy biomarkers. However, the fast-expanding toolkit of spatial proteomic approaches has yet to be systematically applied to investigate pathological alterations in the aging human brain in health and disease states. Moreover, post-mortem human brain tissue presents distinct technical problems due to fixation procedures and autofluorescence, which limit fluorescence methodologies. This study sought to develop a multiplex immunohistochemistry approach (visualizing the immunostain with brightfield microscopy). Quantitative multiplex Immunohistochemistry with Visual colorimetric staining to Enhance Regional protein localization (QUIVER) was developed to address these technical challenges. Using QUIVER, a ten-channel pseudo-fluorescent image was generated using chromogen removal and digital microscopy to identify unique molecular microglia phenotypes. Next, the study asked if the tissue environment, specifically the amyloid plaques and neurofibrillary tangles characteristic of Alzheimer's disease, has any bearing on microglia's cellular and molecular phenotypes. QUIVER allowed the visualization of five molecular microglia/macrophage phenotypes using digital pathology tools. The recognizable reactive and homeostatic microglia/macrophage phenotypes demonstrated spatial polarization towards and away from amyloid plaques, respectively. Yet, microglia morphology appearance did not always correspond to molecular phenotype. This research not only sheds light on the biology of microglia but also offers QUIVER, a new tool for examining pathological alterations in the brains of the elderly.
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spelling pubmed-100248572023-03-20 The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER Shahidehpour, Ryan K. Nelson, Abraham S. Sanders, Lydia G. Embry, Chloe R. Nelson, Peter T. Bachstetter, Adam D. Acta Neuropathol Commun Methodology Article New histological techniques are needed to examine protein distribution in human tissues, which can reveal cell shape and disease pathology connections. Spatial proteomics has changed the study of tumor microenvironments by identifying spatial relationships of immunomodulatory cells and proteins and contributing to the discovery of new cancer immunotherapy biomarkers. However, the fast-expanding toolkit of spatial proteomic approaches has yet to be systematically applied to investigate pathological alterations in the aging human brain in health and disease states. Moreover, post-mortem human brain tissue presents distinct technical problems due to fixation procedures and autofluorescence, which limit fluorescence methodologies. This study sought to develop a multiplex immunohistochemistry approach (visualizing the immunostain with brightfield microscopy). Quantitative multiplex Immunohistochemistry with Visual colorimetric staining to Enhance Regional protein localization (QUIVER) was developed to address these technical challenges. Using QUIVER, a ten-channel pseudo-fluorescent image was generated using chromogen removal and digital microscopy to identify unique molecular microglia phenotypes. Next, the study asked if the tissue environment, specifically the amyloid plaques and neurofibrillary tangles characteristic of Alzheimer's disease, has any bearing on microglia's cellular and molecular phenotypes. QUIVER allowed the visualization of five molecular microglia/macrophage phenotypes using digital pathology tools. The recognizable reactive and homeostatic microglia/macrophage phenotypes demonstrated spatial polarization towards and away from amyloid plaques, respectively. Yet, microglia morphology appearance did not always correspond to molecular phenotype. This research not only sheds light on the biology of microglia but also offers QUIVER, a new tool for examining pathological alterations in the brains of the elderly. BioMed Central 2023-03-18 /pmc/articles/PMC10024857/ /pubmed/36934255 http://dx.doi.org/10.1186/s40478-023-01541-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Shahidehpour, Ryan K.
Nelson, Abraham S.
Sanders, Lydia G.
Embry, Chloe R.
Nelson, Peter T.
Bachstetter, Adam D.
The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title_full The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title_fullStr The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title_full_unstemmed The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title_short The localization of molecularly distinct microglia populations to Alzheimer's disease pathologies using QUIVER
title_sort localization of molecularly distinct microglia populations to alzheimer's disease pathologies using quiver
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10024857/
https://www.ncbi.nlm.nih.gov/pubmed/36934255
http://dx.doi.org/10.1186/s40478-023-01541-w
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