Cargando…

Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells

[Image: see text] Messenger RNA plays a pivotal role in regulating cellular activities. The expression dynamics of specific mRNA contains substantial information on the intracellular milieu. Unlike the imaging of stationary mRNAs, real-time intracellular imaging of the dynamics of mRNA expression is...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Zhe, Zhang, Ruili, Wang, Zhongliang, Wang, He-Fang, Wang, Yu, Zhao, Jun, Wang, Fu, Li, Weitao, Niu, Gang, Kiesewetter, Dale O., Chen, Xiaoyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278684/
https://www.ncbi.nlm.nih.gov/pubmed/25494492
http://dx.doi.org/10.1021/nn505047n
_version_ 1782350551682383872
author Wang, Zhe
Zhang, Ruili
Wang, Zhongliang
Wang, He-Fang
Wang, Yu
Zhao, Jun
Wang, Fu
Li, Weitao
Niu, Gang
Kiesewetter, Dale O.
Chen, Xiaoyuan
author_facet Wang, Zhe
Zhang, Ruili
Wang, Zhongliang
Wang, He-Fang
Wang, Yu
Zhao, Jun
Wang, Fu
Li, Weitao
Niu, Gang
Kiesewetter, Dale O.
Chen, Xiaoyuan
author_sort Wang, Zhe
collection PubMed
description [Image: see text] Messenger RNA plays a pivotal role in regulating cellular activities. The expression dynamics of specific mRNA contains substantial information on the intracellular milieu. Unlike the imaging of stationary mRNAs, real-time intracellular imaging of the dynamics of mRNA expression is of great value for investigating mRNA biology and exploring specific cellular cascades. In addition to advanced imaging methods, timely extracellular stimulation is another key factor in regulating the mRNA expression repertoire. The integration of effective stimulation and imaging into a single robust system would significantly improve stimulation efficiency and imaging accuracy, producing fewer unwanted artifacts. In this study, we developed a multifunctional nanocomplex to enable self-activating and spatiotemporal imaging of the dynamics of mRNA sequential expression during the neural stem cell differentiation process. This nanocomplex showed improved enzymatic stability, fast recognition kinetics, and high specificity. With a mechanism regulated by endogenous cell machinery, this nanocomplex realized the successive stimulating motif release and the dynamic imaging of chronological mRNA expression during neural stem cell differentiation without the use of transgenetic manipulation. The dynamic imaging montage of mRNA expression ultimately facilitated genetic heterogeneity analysis. In vivo lateral ventricle injection of this nanocomplex enabled endogenous neural stem cell activation and labeling at their specific differentiation stages. This nanocomplex is highly amenable as an alternative tool to explore the dynamics of intricate mRNA activities in various physiological and pathological conditions.
format Online
Article
Text
id pubmed-4278684
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-42786842015-12-10 Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells Wang, Zhe Zhang, Ruili Wang, Zhongliang Wang, He-Fang Wang, Yu Zhao, Jun Wang, Fu Li, Weitao Niu, Gang Kiesewetter, Dale O. Chen, Xiaoyuan ACS Nano [Image: see text] Messenger RNA plays a pivotal role in regulating cellular activities. The expression dynamics of specific mRNA contains substantial information on the intracellular milieu. Unlike the imaging of stationary mRNAs, real-time intracellular imaging of the dynamics of mRNA expression is of great value for investigating mRNA biology and exploring specific cellular cascades. In addition to advanced imaging methods, timely extracellular stimulation is another key factor in regulating the mRNA expression repertoire. The integration of effective stimulation and imaging into a single robust system would significantly improve stimulation efficiency and imaging accuracy, producing fewer unwanted artifacts. In this study, we developed a multifunctional nanocomplex to enable self-activating and spatiotemporal imaging of the dynamics of mRNA sequential expression during the neural stem cell differentiation process. This nanocomplex showed improved enzymatic stability, fast recognition kinetics, and high specificity. With a mechanism regulated by endogenous cell machinery, this nanocomplex realized the successive stimulating motif release and the dynamic imaging of chronological mRNA expression during neural stem cell differentiation without the use of transgenetic manipulation. The dynamic imaging montage of mRNA expression ultimately facilitated genetic heterogeneity analysis. In vivo lateral ventricle injection of this nanocomplex enabled endogenous neural stem cell activation and labeling at their specific differentiation stages. This nanocomplex is highly amenable as an alternative tool to explore the dynamics of intricate mRNA activities in various physiological and pathological conditions. American Chemical Society 2014-12-10 2014-12-23 /pmc/articles/PMC4278684/ /pubmed/25494492 http://dx.doi.org/10.1021/nn505047n Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Wang, Zhe
Zhang, Ruili
Wang, Zhongliang
Wang, He-Fang
Wang, Yu
Zhao, Jun
Wang, Fu
Li, Weitao
Niu, Gang
Kiesewetter, Dale O.
Chen, Xiaoyuan
Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title_full Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title_fullStr Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title_full_unstemmed Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title_short Bioinspired Nanocomplex for Spatiotemporal Imaging of Sequential mRNA Expression in Differentiating Neural Stem Cells
title_sort bioinspired nanocomplex for spatiotemporal imaging of sequential mrna expression in differentiating neural stem cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4278684/
https://www.ncbi.nlm.nih.gov/pubmed/25494492
http://dx.doi.org/10.1021/nn505047n
work_keys_str_mv AT wangzhe bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT zhangruili bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT wangzhongliang bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT wanghefang bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT wangyu bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT zhaojun bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT wangfu bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT liweitao bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT niugang bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT kiesewetterdaleo bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells
AT chenxiaoyuan bioinspirednanocomplexforspatiotemporalimagingofsequentialmrnaexpressionindifferentiatingneuralstemcells