An age-wise comparison of human airway smooth muscle proliferative capacity.

We compared the proliferation of neonatal and adult airway smooth muscle cells (ASMC) with no/moderate lung disease, in glucose- (energy production by glycolysis) or glucose-free medium (ATP production from mitochondrial oxidative phosphorylations only), in response to 10% fetal calf serum (FCS) and...

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Main Authors: Michael Fayon, Annick Andrieux, Imane Bara, Muriel Rebola, André Labbé, Roger Marthan, Patrick Berger
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4370680?pdf=render
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author Michael Fayon
Annick Andrieux
Imane Bara
Muriel Rebola
André Labbé
Roger Marthan
Patrick Berger
author_facet Michael Fayon
Annick Andrieux
Imane Bara
Muriel Rebola
André Labbé
Roger Marthan
Patrick Berger
author_sort Michael Fayon
collection DOAJ
description We compared the proliferation of neonatal and adult airway smooth muscle cells (ASMC) with no/moderate lung disease, in glucose- (energy production by glycolysis) or glucose-free medium (ATP production from mitochondrial oxidative phosphorylations only), in response to 10% fetal calf serum (FCS) and PDGF-AA. In the presence of glucose, cell counts were significantly greater in neonatal vs. adult ASMC. Similarly, neonatal ASMC DNA synthesis in 10% FCS and PDGF-AA, and [Ca2+]i responses in the presence of histamine were significantly enhanced vs. adults. In glucose-free medium, cell proliferation was preserved in neonatal cells, unlike in adult cells, with concomitant increased porin (an indicator of mitochondrial activity) protein expression. Compared to adults, stimulated neonatal human ASMC are in a rapid and robust proliferative phase and have the capacity to respond disproportionately under abnormal environmental conditions, through increased mitochondrial biogenesis and altered calcium homeostasis.
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spelling doaj.art-f1b7e2d4b8a4407aa5ee6b8afc5c50412022-12-22T01:03:05ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01103e012244610.1371/journal.pone.0122446An age-wise comparison of human airway smooth muscle proliferative capacity.Michael FayonAnnick AndrieuxImane BaraMuriel RebolaAndré LabbéRoger MarthanPatrick BergerWe compared the proliferation of neonatal and adult airway smooth muscle cells (ASMC) with no/moderate lung disease, in glucose- (energy production by glycolysis) or glucose-free medium (ATP production from mitochondrial oxidative phosphorylations only), in response to 10% fetal calf serum (FCS) and PDGF-AA. In the presence of glucose, cell counts were significantly greater in neonatal vs. adult ASMC. Similarly, neonatal ASMC DNA synthesis in 10% FCS and PDGF-AA, and [Ca2+]i responses in the presence of histamine were significantly enhanced vs. adults. In glucose-free medium, cell proliferation was preserved in neonatal cells, unlike in adult cells, with concomitant increased porin (an indicator of mitochondrial activity) protein expression. Compared to adults, stimulated neonatal human ASMC are in a rapid and robust proliferative phase and have the capacity to respond disproportionately under abnormal environmental conditions, through increased mitochondrial biogenesis and altered calcium homeostasis.http://europepmc.org/articles/PMC4370680?pdf=render
spellingShingle Michael Fayon
Annick Andrieux
Imane Bara
Muriel Rebola
André Labbé
Roger Marthan
Patrick Berger
An age-wise comparison of human airway smooth muscle proliferative capacity.
PLoS ONE
title An age-wise comparison of human airway smooth muscle proliferative capacity.
title_full An age-wise comparison of human airway smooth muscle proliferative capacity.
title_fullStr An age-wise comparison of human airway smooth muscle proliferative capacity.
title_full_unstemmed An age-wise comparison of human airway smooth muscle proliferative capacity.
title_short An age-wise comparison of human airway smooth muscle proliferative capacity.
title_sort age wise comparison of human airway smooth muscle proliferative capacity
url http://europepmc.org/articles/PMC4370680?pdf=render
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