Cargando…
Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction
Multiparameter tissue imaging enables analysis of cell‐cell interactions in situ, the cellular basis for tissue structure, and novel cell types that are spatially restricted, giving clues to biological mechanisms behind tissue homeostasis and disease. Here, we streamlined and simplified the multiple...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251877/ https://www.ncbi.nlm.nih.gov/pubmed/33548142 http://dx.doi.org/10.1002/eji.202048891 |
_version_ | 1783717181991682048 |
---|---|
author | Kennedy‐Darling, Julia Bhate, Salil S. Hickey, John W. Black, Sarah Barlow, Graham L. Vazquez, Gustavo Venkataraaman, Vishal G. Samusik, Nikolay Goltsev, Yury Schürch, Christian M. Nolan, Garry P. |
author_facet | Kennedy‐Darling, Julia Bhate, Salil S. Hickey, John W. Black, Sarah Barlow, Graham L. Vazquez, Gustavo Venkataraaman, Vishal G. Samusik, Nikolay Goltsev, Yury Schürch, Christian M. Nolan, Garry P. |
author_sort | Kennedy‐Darling, Julia |
collection | PubMed |
description | Multiparameter tissue imaging enables analysis of cell‐cell interactions in situ, the cellular basis for tissue structure, and novel cell types that are spatially restricted, giving clues to biological mechanisms behind tissue homeostasis and disease. Here, we streamlined and simplified the multiplexed imaging method CO‐Detection by indEXing (CODEX) by validating 58 unique oligonucleotide barcodes that can be conjugated to antibodies. We showed that barcoded antibodies retained their specificity for staining cognate targets in human tissue. Antibodies were visualized one at a time by adding a fluorescently labeled oligonucleotide complementary to oligonucleotide barcode, imaging, stripping, and repeating this cycle. With this we developed a panel of 46 antibodies that was used to stain five human lymphoid tissues: three tonsils, a spleen, and a LN. To analyze the data produced, an image processing and analysis pipeline was developed that enabled single‐cell analysis on the data, including unsupervised clustering, that revealed 31 cell types across all tissues. We compared cell‐type compositions within and directly surrounding follicles from the different lymphoid organs and evaluated cell‐cell density correlations. This sequential oligonucleotide exchange technique enables a facile imaging of tissues that leverages pre‐existing imaging infrastructure to decrease the barriers to broad use of multiplexed imaging. |
format | Online Article Text |
id | pubmed-8251877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82518772021-07-07 Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction Kennedy‐Darling, Julia Bhate, Salil S. Hickey, John W. Black, Sarah Barlow, Graham L. Vazquez, Gustavo Venkataraaman, Vishal G. Samusik, Nikolay Goltsev, Yury Schürch, Christian M. Nolan, Garry P. Eur J Immunol New technology Multiparameter tissue imaging enables analysis of cell‐cell interactions in situ, the cellular basis for tissue structure, and novel cell types that are spatially restricted, giving clues to biological mechanisms behind tissue homeostasis and disease. Here, we streamlined and simplified the multiplexed imaging method CO‐Detection by indEXing (CODEX) by validating 58 unique oligonucleotide barcodes that can be conjugated to antibodies. We showed that barcoded antibodies retained their specificity for staining cognate targets in human tissue. Antibodies were visualized one at a time by adding a fluorescently labeled oligonucleotide complementary to oligonucleotide barcode, imaging, stripping, and repeating this cycle. With this we developed a panel of 46 antibodies that was used to stain five human lymphoid tissues: three tonsils, a spleen, and a LN. To analyze the data produced, an image processing and analysis pipeline was developed that enabled single‐cell analysis on the data, including unsupervised clustering, that revealed 31 cell types across all tissues. We compared cell‐type compositions within and directly surrounding follicles from the different lymphoid organs and evaluated cell‐cell density correlations. This sequential oligonucleotide exchange technique enables a facile imaging of tissues that leverages pre‐existing imaging infrastructure to decrease the barriers to broad use of multiplexed imaging. John Wiley and Sons Inc. 2021-03-10 2021-05 /pmc/articles/PMC8251877/ /pubmed/33548142 http://dx.doi.org/10.1002/eji.202048891 Text en © 2021 The Authors. European Journal of Immunology published by Wiley‐VCH GmbH 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 | New technology Kennedy‐Darling, Julia Bhate, Salil S. Hickey, John W. Black, Sarah Barlow, Graham L. Vazquez, Gustavo Venkataraaman, Vishal G. Samusik, Nikolay Goltsev, Yury Schürch, Christian M. Nolan, Garry P. Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title | Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title_full | Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title_fullStr | Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title_full_unstemmed | Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title_short | Highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
title_sort | highly multiplexed tissue imaging using repeated oligonucleotide exchange reaction |
topic | New technology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8251877/ https://www.ncbi.nlm.nih.gov/pubmed/33548142 http://dx.doi.org/10.1002/eji.202048891 |
work_keys_str_mv | AT kennedydarlingjulia highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT bhatesalils highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT hickeyjohnw highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT blacksarah highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT barlowgrahaml highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT vazquezgustavo highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT venkataraamanvishalg highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT samusiknikolay highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT goltsevyury highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT schurchchristianm highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction AT nolangarryp highlymultiplexedtissueimagingusingrepeatedoligonucleotideexchangereaction |