Cargando…
Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis
Complex tissues such as the lung are composed of structural hierarchies such as alveoli, alveolar ducts, and lobules. Some structural units, such as the alveolar duct, appear to participate in tissue repair as well as the development of bronchioalveolar carcinoma. Here, we demonstrate an approach to...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173809/ https://www.ncbi.nlm.nih.gov/pubmed/25309876 http://dx.doi.org/10.3389/fonc.2014.00260 |
_version_ | 1782336264799780864 |
---|---|
author | Bennett, Robert D. Ysasi, Alexandra B. Belle, Janeil M. Wagner, Willi L. Konerding, Moritz A. Blainey, Paul C. Pyne, Saumyadipta Mentzer, Steven J. |
author_facet | Bennett, Robert D. Ysasi, Alexandra B. Belle, Janeil M. Wagner, Willi L. Konerding, Moritz A. Blainey, Paul C. Pyne, Saumyadipta Mentzer, Steven J. |
author_sort | Bennett, Robert D. |
collection | PubMed |
description | Complex tissues such as the lung are composed of structural hierarchies such as alveoli, alveolar ducts, and lobules. Some structural units, such as the alveolar duct, appear to participate in tissue repair as well as the development of bronchioalveolar carcinoma. Here, we demonstrate an approach to conduct laser microdissection of the lung alveolar duct for single-cell PCR analysis. Our approach involved three steps. (1) The initial preparation used mechanical sectioning of the lung tissue with sufficient thickness to encompass the structure of interest. In the case of the alveolar duct, the precision-cut lung slices were 200 μm thick; the slices were processed using near-physiologic conditions to preserve the state of viable cells. (2) The lung slices were examined by transmission light microscopy to target the alveolar duct. The air-filled lung was sufficiently accessible by light microscopy that counterstains or fluorescent labels were unnecessary to identify the alveolar duct. (3) The enzymatic and microfluidic isolation of single cells allowed for the harvest of as few as several thousand cells for PCR analysis. Microfluidics based arrays were used to measure the expression of selected marker genes in individual cells to characterize different cell populations. Preliminary work suggests the unique value of this approach to understand the intra- and intercellular interactions within the regenerating alveolar duct. |
format | Online Article Text |
id | pubmed-4173809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41738092014-10-10 Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis Bennett, Robert D. Ysasi, Alexandra B. Belle, Janeil M. Wagner, Willi L. Konerding, Moritz A. Blainey, Paul C. Pyne, Saumyadipta Mentzer, Steven J. Front Oncol Oncology Complex tissues such as the lung are composed of structural hierarchies such as alveoli, alveolar ducts, and lobules. Some structural units, such as the alveolar duct, appear to participate in tissue repair as well as the development of bronchioalveolar carcinoma. Here, we demonstrate an approach to conduct laser microdissection of the lung alveolar duct for single-cell PCR analysis. Our approach involved three steps. (1) The initial preparation used mechanical sectioning of the lung tissue with sufficient thickness to encompass the structure of interest. In the case of the alveolar duct, the precision-cut lung slices were 200 μm thick; the slices were processed using near-physiologic conditions to preserve the state of viable cells. (2) The lung slices were examined by transmission light microscopy to target the alveolar duct. The air-filled lung was sufficiently accessible by light microscopy that counterstains or fluorescent labels were unnecessary to identify the alveolar duct. (3) The enzymatic and microfluidic isolation of single cells allowed for the harvest of as few as several thousand cells for PCR analysis. Microfluidics based arrays were used to measure the expression of selected marker genes in individual cells to characterize different cell populations. Preliminary work suggests the unique value of this approach to understand the intra- and intercellular interactions within the regenerating alveolar duct. Frontiers Media S.A. 2014-09-24 /pmc/articles/PMC4173809/ /pubmed/25309876 http://dx.doi.org/10.3389/fonc.2014.00260 Text en Copyright © 2014 Bennett, Ysasi, Belle, Wagner, Konerding, Blainey, Pyne and Mentzer. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Bennett, Robert D. Ysasi, Alexandra B. Belle, Janeil M. Wagner, Willi L. Konerding, Moritz A. Blainey, Paul C. Pyne, Saumyadipta Mentzer, Steven J. Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title | Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title_full | Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title_fullStr | Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title_full_unstemmed | Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title_short | Laser Microdissection of the Alveolar Duct Enables Single-Cell Genomic Analysis |
title_sort | laser microdissection of the alveolar duct enables single-cell genomic analysis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173809/ https://www.ncbi.nlm.nih.gov/pubmed/25309876 http://dx.doi.org/10.3389/fonc.2014.00260 |
work_keys_str_mv | AT bennettrobertd lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT ysasialexandrab lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT bellejaneilm lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT wagnerwillil lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT konerdingmoritza lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT blaineypaulc lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT pynesaumyadipta lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis AT mentzerstevenj lasermicrodissectionofthealveolarductenablessinglecellgenomicanalysis |