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Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy

There is a growing body of evidence that innate immunity also plays an important role in the progression of hepatitis B virus (HBV) infection. However, there is less study on systematically elucidating the characteristics of innate immunity in HBV‐infected pregnant women. We compared the features of...

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Autores principales: Wang, Hongyan, Li, Xia, Yang, Kaiyue, Guo, Fanfan, Wang, Xiaona, Zhao, Ziyan, Jia, Yanju, Gao, Fan, Bai, Guiqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243157/
https://www.ncbi.nlm.nih.gov/pubmed/37078407
http://dx.doi.org/10.1111/jcmm.17746
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author Wang, Hongyan
Li, Xia
Yang, Kaiyue
Guo, Fanfan
Wang, Xiaona
Zhao, Ziyan
Jia, Yanju
Gao, Fan
Bai, Guiqin
author_facet Wang, Hongyan
Li, Xia
Yang, Kaiyue
Guo, Fanfan
Wang, Xiaona
Zhao, Ziyan
Jia, Yanju
Gao, Fan
Bai, Guiqin
author_sort Wang, Hongyan
collection PubMed
description There is a growing body of evidence that innate immunity also plays an important role in the progression of hepatitis B virus (HBV) infection. However, there is less study on systematically elucidating the characteristics of innate immunity in HBV‐infected pregnant women. We compared the features of peripheral blood mononuclear cells in three healthy pregnant women and three HBV‐infected pregnant women by single‐cell RNA sequencing. 10 DEGs were detected between groups and monocytes were the main expression source of most of the DEGs, which involved in the inflammatory response, apoptosis and immune regulation. Meanwhile, qPCR and ELISA were performed to verify above genes. Monocytes displayed immune response defect, reflecting poor ability of response to IFN. In addition, eight clusters were identified in monocytes. We identified molecular drivers in monocytes subpopulations.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes were featured with different gene expression pattern and biological function.TNFSF10+ monocytes and MT1G+ monocytes were characterized by high levels of inflammation response.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes showed decreased response to IFN. Our results dissects alterations in monocytes related to the immune response of HBV‐infected pregnant women and provides a rich resource for fully understanding immunopathogenesis and developing effective preventing HBV intrauterine infection strategies.
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spelling pubmed-102431572023-06-07 Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy Wang, Hongyan Li, Xia Yang, Kaiyue Guo, Fanfan Wang, Xiaona Zhao, Ziyan Jia, Yanju Gao, Fan Bai, Guiqin J Cell Mol Med Original Articles There is a growing body of evidence that innate immunity also plays an important role in the progression of hepatitis B virus (HBV) infection. However, there is less study on systematically elucidating the characteristics of innate immunity in HBV‐infected pregnant women. We compared the features of peripheral blood mononuclear cells in three healthy pregnant women and three HBV‐infected pregnant women by single‐cell RNA sequencing. 10 DEGs were detected between groups and monocytes were the main expression source of most of the DEGs, which involved in the inflammatory response, apoptosis and immune regulation. Meanwhile, qPCR and ELISA were performed to verify above genes. Monocytes displayed immune response defect, reflecting poor ability of response to IFN. In addition, eight clusters were identified in monocytes. We identified molecular drivers in monocytes subpopulations.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes were featured with different gene expression pattern and biological function.TNFSF10+ monocytes and MT1G+ monocytes were characterized by high levels of inflammation response.TNFSF10+ monocytes, MT1G+ monocytes and TUBB1+ monocytes showed decreased response to IFN. Our results dissects alterations in monocytes related to the immune response of HBV‐infected pregnant women and provides a rich resource for fully understanding immunopathogenesis and developing effective preventing HBV intrauterine infection strategies. John Wiley and Sons Inc. 2023-04-20 /pmc/articles/PMC10243157/ /pubmed/37078407 http://dx.doi.org/10.1111/jcmm.17746 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Hongyan
Li, Xia
Yang, Kaiyue
Guo, Fanfan
Wang, Xiaona
Zhao, Ziyan
Jia, Yanju
Gao, Fan
Bai, Guiqin
Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title_full Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title_fullStr Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title_full_unstemmed Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title_short Single‐cell RNA sequencing reveals transcriptional profiles of monocytes in HBV‐infected pregnant women during mid‐pregnancy
title_sort single‐cell rna sequencing reveals transcriptional profiles of monocytes in hbv‐infected pregnant women during mid‐pregnancy
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10243157/
https://www.ncbi.nlm.nih.gov/pubmed/37078407
http://dx.doi.org/10.1111/jcmm.17746
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