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The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue

Using the Toponome Imaging System (TIS), a serial immunostainer, we studied the patterns of expression of multiple markers in alveolar macrophages (AM) from female mice lacking surfactant protein A (SP-A knockouts; KO) after “rescue” with exogenous SP-A1. We also used a 7-marker subset to compare wi...

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Autores principales: Phelps, David S., Chinchilli, Vernon M., Yang, Lili, Shearer, Debra, Weisz, Judith, Zhang, Xuesheng, Floros, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943067/
https://www.ncbi.nlm.nih.gov/pubmed/35322074
http://dx.doi.org/10.1038/s41598-022-08114-2
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author Phelps, David S.
Chinchilli, Vernon M.
Yang, Lili
Shearer, Debra
Weisz, Judith
Zhang, Xuesheng
Floros, Joanna
author_facet Phelps, David S.
Chinchilli, Vernon M.
Yang, Lili
Shearer, Debra
Weisz, Judith
Zhang, Xuesheng
Floros, Joanna
author_sort Phelps, David S.
collection PubMed
description Using the Toponome Imaging System (TIS), a serial immunostainer, we studied the patterns of expression of multiple markers in alveolar macrophages (AM) from female mice lacking surfactant protein A (SP-A knockouts; KO) after “rescue” with exogenous SP-A1. We also used a 7-marker subset to compare with AM from males. AM were harvested 18 h after intrapharyngeal SP-A1 or vehicle, attached to slides, and subjected to serial immunostaining for 12 markers. Expression of the markers in each pixel of the image was analyzed both in the whole image and in individual selected cells. The marker combination in each pixel is referred to as a combinatorial molecular phenotype (CMP). A subset of antibodies was used to compare AM from male mice to the females. We found: (a) extensive AM heterogeneity in females by CMP analysis and by clustering analysis of CMPs in single cells; (b) AM from female KO mice respond to exogenous SP-A1 by increasing CMP phenotypic diversity and perhaps enhancing their potential innate immune capabilities; and (c) comparison of male and female AM responses to SP-A1 revealed that males respond more vigorously than females and clustering analysis was more effective in distinguishing males from females rather than treated from control.
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spelling pubmed-89430672022-03-28 The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue Phelps, David S. Chinchilli, Vernon M. Yang, Lili Shearer, Debra Weisz, Judith Zhang, Xuesheng Floros, Joanna Sci Rep Article Using the Toponome Imaging System (TIS), a serial immunostainer, we studied the patterns of expression of multiple markers in alveolar macrophages (AM) from female mice lacking surfactant protein A (SP-A knockouts; KO) after “rescue” with exogenous SP-A1. We also used a 7-marker subset to compare with AM from males. AM were harvested 18 h after intrapharyngeal SP-A1 or vehicle, attached to slides, and subjected to serial immunostaining for 12 markers. Expression of the markers in each pixel of the image was analyzed both in the whole image and in individual selected cells. The marker combination in each pixel is referred to as a combinatorial molecular phenotype (CMP). A subset of antibodies was used to compare AM from male mice to the females. We found: (a) extensive AM heterogeneity in females by CMP analysis and by clustering analysis of CMPs in single cells; (b) AM from female KO mice respond to exogenous SP-A1 by increasing CMP phenotypic diversity and perhaps enhancing their potential innate immune capabilities; and (c) comparison of male and female AM responses to SP-A1 revealed that males respond more vigorously than females and clustering analysis was more effective in distinguishing males from females rather than treated from control. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943067/ /pubmed/35322074 http://dx.doi.org/10.1038/s41598-022-08114-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/) .
spellingShingle Article
Phelps, David S.
Chinchilli, Vernon M.
Yang, Lili
Shearer, Debra
Weisz, Judith
Zhang, Xuesheng
Floros, Joanna
The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title_full The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title_fullStr The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title_full_unstemmed The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title_short The alveolar macrophage toponome of female SP-A knockout mice differs from that of males before and after SP-A1 rescue
title_sort alveolar macrophage toponome of female sp-a knockout mice differs from that of males before and after sp-a1 rescue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943067/
https://www.ncbi.nlm.nih.gov/pubmed/35322074
http://dx.doi.org/10.1038/s41598-022-08114-2
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