Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.

The therapeutic potential of stem cells is limited by the non-uniformity of their phenotypic state. Thus it would be advantageous to noninvasively monitor stem cell status. Driven by this challenge, we employed multidimensional multiphoton microscopy to quantify changes in endogenous fluorescence oc...

Full description

Bibliographic Details
Main Authors: Jayne M Squirrell, Jimmy J Fong, Carlos A Ariza, Amber Mael, Kassondra Meyer, Nirupama K Shevde, Avtar Roopra, Gary E Lyons, Timothy J Kamp, Kevin W Eliceiri, Brenda M Ogle
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3430704?pdf=render
id doaj-36ef4ca9d3c44326a4d66fe5b8c8a324
record_format Article
spelling doaj-36ef4ca9d3c44326a4d66fe5b8c8a3242020-11-25T00:23:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4370810.1371/journal.pone.0043708Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.Jayne M SquirrellJimmy J FongCarlos A ArizaAmber MaelKassondra MeyerNirupama K ShevdeAvtar RoopraGary E LyonsTimothy J KampKevin W EliceiriBrenda M OgleThe therapeutic potential of stem cells is limited by the non-uniformity of their phenotypic state. Thus it would be advantageous to noninvasively monitor stem cell status. Driven by this challenge, we employed multidimensional multiphoton microscopy to quantify changes in endogenous fluorescence occurring with pluripotent stem cell differentiation. We found that global and cellular-scale fluorescence lifetime of human embryonic stem cells (hESC) and murine embryonic stem cells (mESC) consistently decreased with differentiation. Less consistent were trends in endogenous fluorescence intensity with differentiation, suggesting intensity is more readily impacted by nuances of species and scale of analysis. What emerges is a practical and accessible approach to evaluate, and ultimately enrich, living stem cell populations based on changes in metabolism that could be exploited for both research and clinical applications.http://europepmc.org/articles/PMC3430704?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jayne M Squirrell
Jimmy J Fong
Carlos A Ariza
Amber Mael
Kassondra Meyer
Nirupama K Shevde
Avtar Roopra
Gary E Lyons
Timothy J Kamp
Kevin W Eliceiri
Brenda M Ogle
spellingShingle Jayne M Squirrell
Jimmy J Fong
Carlos A Ariza
Amber Mael
Kassondra Meyer
Nirupama K Shevde
Avtar Roopra
Gary E Lyons
Timothy J Kamp
Kevin W Eliceiri
Brenda M Ogle
Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
PLoS ONE
author_facet Jayne M Squirrell
Jimmy J Fong
Carlos A Ariza
Amber Mael
Kassondra Meyer
Nirupama K Shevde
Avtar Roopra
Gary E Lyons
Timothy J Kamp
Kevin W Eliceiri
Brenda M Ogle
author_sort Jayne M Squirrell
title Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
title_short Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
title_full Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
title_fullStr Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
title_full_unstemmed Endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
title_sort endogenous fluorescence signatures in living pluripotent stem cells change with loss of potency.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The therapeutic potential of stem cells is limited by the non-uniformity of their phenotypic state. Thus it would be advantageous to noninvasively monitor stem cell status. Driven by this challenge, we employed multidimensional multiphoton microscopy to quantify changes in endogenous fluorescence occurring with pluripotent stem cell differentiation. We found that global and cellular-scale fluorescence lifetime of human embryonic stem cells (hESC) and murine embryonic stem cells (mESC) consistently decreased with differentiation. Less consistent were trends in endogenous fluorescence intensity with differentiation, suggesting intensity is more readily impacted by nuances of species and scale of analysis. What emerges is a practical and accessible approach to evaluate, and ultimately enrich, living stem cell populations based on changes in metabolism that could be exploited for both research and clinical applications.
url http://europepmc.org/articles/PMC3430704?pdf=render
work_keys_str_mv AT jaynemsquirrell endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT jimmyjfong endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT carlosaariza endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT ambermael endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT kassondrameyer endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT nirupamakshevde endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT avtarroopra endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT garyelyons endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT timothyjkamp endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT kevinweliceiri endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
AT brendamogle endogenousfluorescencesignaturesinlivingpluripotentstemcellschangewithlossofpotency
_version_ 1725357248482377728