“High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”

Abstract The tissue-specific etiology of aging and stress has been elusive due to limitations in data processing of current techniques. Despite that many techniques are high-throughput, they usually use singular features of the data (e.g. whole fluorescence). One technology at the nexus of fluoresce...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Joseph R. Daniele, Daniel J. Esping, Gilbert Garcia, Lee S. Parsons, Edgar A. Arriaga, Andrew Dillin
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/161665a6154340f8869de5212ae2387f
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:161665a6154340f8869de5212ae2387f
record_format dspace
spelling oai:doaj.org-article:161665a6154340f8869de5212ae2387f2021-12-02T11:52:15Z“High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”10.1038/s41598-017-05152-z2045-2322https://doaj.org/article/161665a6154340f8869de5212ae2387f2017-07-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-05152-zhttps://doaj.org/toc/2045-2322Abstract The tissue-specific etiology of aging and stress has been elusive due to limitations in data processing of current techniques. Despite that many techniques are high-throughput, they usually use singular features of the data (e.g. whole fluorescence). One technology at the nexus of fluorescence-based screens is large particle flow cytometry (“biosorter”), capable of recording positional fluorescence and object granularity information from many individual live animals. Current processing of biosorter data, however, do not integrate positional information into their analysis and data visualization. Here, we present a bioanalytical platform for the quantification of positional information (“longitudinal profiling”) of C. elegans, which we posit embodies the benefits of both high-throughput screening and high-resolution microscopy. We show the use of these techniques in (1) characterizing distinct responses of a transcriptional reporter to various stresses in defined anatomical regions, (2) identifying regions of high mitochondrial membrane potential in live animals, (3) monitoring regional mitochondrial activity in aging models and during development, and (4) screening for regulators of muscle mitochondrial dynamics in a high-throughput format. This platform offers a significant improvement in the quality of high-throughput biosorter data analysis and visualization, opening new options for region-specific phenotypic screening of complex physiological phenomena and mitochondrial biology.Joseph R. DanieleDaniel J. EspingGilbert GarciaLee S. ParsonsEdgar A. ArriagaAndrew DillinNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Joseph R. Daniele
Daniel J. Esping
Gilbert Garcia
Lee S. Parsons
Edgar A. Arriaga
Andrew Dillin
“High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
description Abstract The tissue-specific etiology of aging and stress has been elusive due to limitations in data processing of current techniques. Despite that many techniques are high-throughput, they usually use singular features of the data (e.g. whole fluorescence). One technology at the nexus of fluorescence-based screens is large particle flow cytometry (“biosorter”), capable of recording positional fluorescence and object granularity information from many individual live animals. Current processing of biosorter data, however, do not integrate positional information into their analysis and data visualization. Here, we present a bioanalytical platform for the quantification of positional information (“longitudinal profiling”) of C. elegans, which we posit embodies the benefits of both high-throughput screening and high-resolution microscopy. We show the use of these techniques in (1) characterizing distinct responses of a transcriptional reporter to various stresses in defined anatomical regions, (2) identifying regions of high mitochondrial membrane potential in live animals, (3) monitoring regional mitochondrial activity in aging models and during development, and (4) screening for regulators of muscle mitochondrial dynamics in a high-throughput format. This platform offers a significant improvement in the quality of high-throughput biosorter data analysis and visualization, opening new options for region-specific phenotypic screening of complex physiological phenomena and mitochondrial biology.
format article
author Joseph R. Daniele
Daniel J. Esping
Gilbert Garcia
Lee S. Parsons
Edgar A. Arriaga
Andrew Dillin
author_facet Joseph R. Daniele
Daniel J. Esping
Gilbert Garcia
Lee S. Parsons
Edgar A. Arriaga
Andrew Dillin
author_sort Joseph R. Daniele
title “High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
title_short “High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
title_full “High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
title_fullStr “High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
title_full_unstemmed “High-Throughput Characterization of Region-Specific Mitochondrial Function and Morphology”
title_sort “high-throughput characterization of region-specific mitochondrial function and morphology”
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/161665a6154340f8869de5212ae2387f
work_keys_str_mv AT josephrdaniele highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
AT danieljesping highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
AT gilbertgarcia highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
AT leesparsons highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
AT edgaraarriaga highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
AT andrewdillin highthroughputcharacterizationofregionspecificmitochondrialfunctionandmorphology
_version_ 1718395089510727680