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HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages

Macrophages are key elements of the innate immune system. Their HIV-1 infection is a complex process that involves multiple interacting factors and various steps and is further altered by exposure of infected cells to methamphetamine (Meth), a common drug of abuse in people living with HIV. This is...

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Autores principales: Grabowska, Kinga, Macur, Katarzyna, Zieschang, Sarah, Zaman, Lubaba, Haverland, Nicole, Schissel, Andrew, Morsey, Brenda, Fox, Howard S., Ciborowski, Pawel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076712/
https://www.ncbi.nlm.nih.gov/pubmed/35175539
http://dx.doi.org/10.1007/s13365-021-01025-4
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author Grabowska, Kinga
Macur, Katarzyna
Zieschang, Sarah
Zaman, Lubaba
Haverland, Nicole
Schissel, Andrew
Morsey, Brenda
Fox, Howard S.
Ciborowski, Pawel
author_facet Grabowska, Kinga
Macur, Katarzyna
Zieschang, Sarah
Zaman, Lubaba
Haverland, Nicole
Schissel, Andrew
Morsey, Brenda
Fox, Howard S.
Ciborowski, Pawel
author_sort Grabowska, Kinga
collection PubMed
description Macrophages are key elements of the innate immune system. Their HIV-1 infection is a complex process that involves multiple interacting factors and various steps and is further altered by exposure of infected cells to methamphetamine (Meth), a common drug of abuse in people living with HIV. This is reflected by dynamic changes in the intracellular and secreted proteomes of these cells. Quantification of these changes poses a challenge for experimental design and associated analytics. In this study, we measured the effect of Meth on expression of intracellular and secreted galectins-1, -3, and -9 in HIV-1 infected human monocyte-derived macrophages (hMDM) using SWATH-MS, which was further followed by MRM targeted mass spectrometry validation. Cells were exposed to Meth either prior to or after infection. Our results are the first to perform comprehensive quantifications of galectins in primary hMDM cells during HIV-1 infection and Meth exposure a building foundation for future studies on the molecular mechanisms underlying cellular pathology of hMDM resulting from viral infection and a drug of abuse—Meth. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13365-021-01025-4.
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spelling pubmed-90767122022-05-08 HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages Grabowska, Kinga Macur, Katarzyna Zieschang, Sarah Zaman, Lubaba Haverland, Nicole Schissel, Andrew Morsey, Brenda Fox, Howard S. Ciborowski, Pawel J Neurovirol Article Macrophages are key elements of the innate immune system. Their HIV-1 infection is a complex process that involves multiple interacting factors and various steps and is further altered by exposure of infected cells to methamphetamine (Meth), a common drug of abuse in people living with HIV. This is reflected by dynamic changes in the intracellular and secreted proteomes of these cells. Quantification of these changes poses a challenge for experimental design and associated analytics. In this study, we measured the effect of Meth on expression of intracellular and secreted galectins-1, -3, and -9 in HIV-1 infected human monocyte-derived macrophages (hMDM) using SWATH-MS, which was further followed by MRM targeted mass spectrometry validation. Cells were exposed to Meth either prior to or after infection. Our results are the first to perform comprehensive quantifications of galectins in primary hMDM cells during HIV-1 infection and Meth exposure a building foundation for future studies on the molecular mechanisms underlying cellular pathology of hMDM resulting from viral infection and a drug of abuse—Meth. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13365-021-01025-4. Springer International Publishing 2022-02-17 2022 /pmc/articles/PMC9076712/ /pubmed/35175539 http://dx.doi.org/10.1007/s13365-021-01025-4 Text en © The Author(s) 2022 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/) .
spellingShingle Article
Grabowska, Kinga
Macur, Katarzyna
Zieschang, Sarah
Zaman, Lubaba
Haverland, Nicole
Schissel, Andrew
Morsey, Brenda
Fox, Howard S.
Ciborowski, Pawel
HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title_full HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title_fullStr HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title_full_unstemmed HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title_short HIV-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
title_sort hiv-1 and methamphetamine alter galectins -1, -3, and -9 in human monocyte-derived macrophages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9076712/
https://www.ncbi.nlm.nih.gov/pubmed/35175539
http://dx.doi.org/10.1007/s13365-021-01025-4
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