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Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells

Noninvasive prenatal diagnosis (NIPD) aims to detect fetal-related genetic disorders before birth by detecting markers in the peripheral blood of pregnant women, holding the potential in reducing the risk of fetal birth defects. Fetal-nucleated red blood cells (fNRBCs) can be used as biomarkers for...

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Autores principales: Chen, Yanyu, Wu, Zhuhao, Sutlive, Joseph, Wu, Ke, Mao, Lu, Nie, Jiabao, Zhao, Xing-Zhong, Guo, Feng, Chen, Zi, Huang, Qinqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805221/
https://www.ncbi.nlm.nih.gov/pubmed/36585678
http://dx.doi.org/10.1186/s12951-022-01749-3
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author Chen, Yanyu
Wu, Zhuhao
Sutlive, Joseph
Wu, Ke
Mao, Lu
Nie, Jiabao
Zhao, Xing-Zhong
Guo, Feng
Chen, Zi
Huang, Qinqin
author_facet Chen, Yanyu
Wu, Zhuhao
Sutlive, Joseph
Wu, Ke
Mao, Lu
Nie, Jiabao
Zhao, Xing-Zhong
Guo, Feng
Chen, Zi
Huang, Qinqin
author_sort Chen, Yanyu
collection PubMed
description Noninvasive prenatal diagnosis (NIPD) aims to detect fetal-related genetic disorders before birth by detecting markers in the peripheral blood of pregnant women, holding the potential in reducing the risk of fetal birth defects. Fetal-nucleated red blood cells (fNRBCs) can be used as biomarkers for NIPD, given their remarkable nature of carrying the entire genetic information of the fetus. Here, we review recent advances in NIPD technologies based on the isolation and analysis of fNRBCs. Conventional cell separation methods rely primarily on physical properties and surface antigens of fNRBCs, such as density gradient centrifugation, fluorescence-activated cell sorting, and magnetic-activated cell sorting. Due to the limitations of sensitivity and purity in Conventional methods, separation techniques based on micro-/nanomaterials have been developed as novel methods for isolating and enriching fNRBCs. We also discuss emerging methods based on microfluidic chips and nanostructured substrates for static and dynamic isolation of fNRBCs. Additionally, we introduce the identification techniques of fNRBCs and address the potential clinical diagnostic values of fNRBCs. Finally, we highlight the challenges and the future directions of fNRBCs as treatment guidelines in NIPD. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-98052212023-01-01 Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells Chen, Yanyu Wu, Zhuhao Sutlive, Joseph Wu, Ke Mao, Lu Nie, Jiabao Zhao, Xing-Zhong Guo, Feng Chen, Zi Huang, Qinqin J Nanobiotechnology Review Noninvasive prenatal diagnosis (NIPD) aims to detect fetal-related genetic disorders before birth by detecting markers in the peripheral blood of pregnant women, holding the potential in reducing the risk of fetal birth defects. Fetal-nucleated red blood cells (fNRBCs) can be used as biomarkers for NIPD, given their remarkable nature of carrying the entire genetic information of the fetus. Here, we review recent advances in NIPD technologies based on the isolation and analysis of fNRBCs. Conventional cell separation methods rely primarily on physical properties and surface antigens of fNRBCs, such as density gradient centrifugation, fluorescence-activated cell sorting, and magnetic-activated cell sorting. Due to the limitations of sensitivity and purity in Conventional methods, separation techniques based on micro-/nanomaterials have been developed as novel methods for isolating and enriching fNRBCs. We also discuss emerging methods based on microfluidic chips and nanostructured substrates for static and dynamic isolation of fNRBCs. Additionally, we introduce the identification techniques of fNRBCs and address the potential clinical diagnostic values of fNRBCs. Finally, we highlight the challenges and the future directions of fNRBCs as treatment guidelines in NIPD. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-12-30 /pmc/articles/PMC9805221/ /pubmed/36585678 http://dx.doi.org/10.1186/s12951-022-01749-3 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/) . 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 Review
Chen, Yanyu
Wu, Zhuhao
Sutlive, Joseph
Wu, Ke
Mao, Lu
Nie, Jiabao
Zhao, Xing-Zhong
Guo, Feng
Chen, Zi
Huang, Qinqin
Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title_full Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title_fullStr Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title_full_unstemmed Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title_short Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
title_sort noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805221/
https://www.ncbi.nlm.nih.gov/pubmed/36585678
http://dx.doi.org/10.1186/s12951-022-01749-3
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