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Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression

Peripheral T cells are in G0 phase and do not proliferate. When they encounter an antigen, they enter the cell cycle and proliferate in order to initiate an active immune response. Here, we have determined the first two cell cycle times of a leading population of CD4(+) T cells stimulated by PMA plu...

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Autores principales: Mishima, Takuya, Toda, Shoko, Ando, Yoshiaki, Matsunaga, Tsukasa, Inobe, Manabu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Versita 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275717/
https://www.ncbi.nlm.nih.gov/pubmed/25424911
http://dx.doi.org/10.2478/s11658-014-0219-z
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author Mishima, Takuya
Toda, Shoko
Ando, Yoshiaki
Matsunaga, Tsukasa
Inobe, Manabu
author_facet Mishima, Takuya
Toda, Shoko
Ando, Yoshiaki
Matsunaga, Tsukasa
Inobe, Manabu
author_sort Mishima, Takuya
collection PubMed
description Peripheral T cells are in G0 phase and do not proliferate. When they encounter an antigen, they enter the cell cycle and proliferate in order to initiate an active immune response. Here, we have determined the first two cell cycle times of a leading population of CD4(+) T cells stimulated by PMA plus ionomycin in vitro. The first cell cycle began around 10 h after stimulation and took approximately 16 h. Surprisingly, the second cell cycle was extremely rapid and required only 6 h. T cells might have a unique regulatory mechanism to compensate for the shortage of the gap phases in cell cycle progression. This unique feature might be a basis for a quick immune response against pathogens, as it maximizes the rate of proliferation.
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spelling pubmed-62757172018-12-10 Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression Mishima, Takuya Toda, Shoko Ando, Yoshiaki Matsunaga, Tsukasa Inobe, Manabu Cell Mol Biol Lett Research Article Peripheral T cells are in G0 phase and do not proliferate. When they encounter an antigen, they enter the cell cycle and proliferate in order to initiate an active immune response. Here, we have determined the first two cell cycle times of a leading population of CD4(+) T cells stimulated by PMA plus ionomycin in vitro. The first cell cycle began around 10 h after stimulation and took approximately 16 h. Surprisingly, the second cell cycle was extremely rapid and required only 6 h. T cells might have a unique regulatory mechanism to compensate for the shortage of the gap phases in cell cycle progression. This unique feature might be a basis for a quick immune response against pathogens, as it maximizes the rate of proliferation. Versita 2014-11-25 /pmc/articles/PMC6275717/ /pubmed/25424911 http://dx.doi.org/10.2478/s11658-014-0219-z Text en © Versita Warsaw and Springer-Verlag Wien 2014
spellingShingle Research Article
Mishima, Takuya
Toda, Shoko
Ando, Yoshiaki
Matsunaga, Tsukasa
Inobe, Manabu
Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title_full Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title_fullStr Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title_full_unstemmed Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title_short Rapid proliferation of activated lymph node CD4(+) T cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
title_sort rapid proliferation of activated lymph node cd4(+) t cells is achieved by greatly curtailing the duration of gap phases in cell cycle progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275717/
https://www.ncbi.nlm.nih.gov/pubmed/25424911
http://dx.doi.org/10.2478/s11658-014-0219-z
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