Форма представления | Статьи в зарубежных журналах и сборниках |
Год публикации | 2017 |
Язык | английский |
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Котов Николай Викторович, автор
Салахиева Диана Витальевна, автор
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I. I Sadreev , Michael Z, Q Chen , Yoshinori Umezawa , Claudia Kemper, Gavin I Welsh Ildar I, автор
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Библиографическое описание на языке оригинала |
Ildar I Sadreev, The competitive nature of STAT complex formation drives phenotype switching of T cells /Ildar I Sadreev, Michael Z Q Chen, Yoshinori Umezawa, Vadim N Biktashev, Claudia Kemper, Diana V Salakhieva, Gavin I Welsh, Nikolay V Kotov.-2017.-Cite as: arXiv:1701.05503 [q-bio.MN] |
Аннотация |
Signal transducers and activators of transcription (STATs) are key molecular determinants of T cell fate and effector function. A number of inflammatory diseases are characterized by an altered balance of T cell phenotypes and cytokine secretion. STATs, therefore, represent viable therapeutic targets in numerous pathologies. However, the underlying mechanisms of how the same STAT proteins regulate both the development of different T cell phenotypes and their plasticity during changes in extracellular conditions remain unclear. In this study, we investigated the STAT mediated regulation of T cell phenotype formation and plasticity using mathematical modeling and experimental data for intracellular STAT signaling proteins. The close fit of our model predictions to the experimental data for IFN-{\gamma} to IL-10 switching allows us to propose a potential mechanism for T cell switching that regulates human Th1/Tr1 responses. According to this mechanism, T cell phenotype switching is due to |
Ключевые слова |
Quantitative Biology, Molecular Networks |
Название журнала |
IMMUNOLOGY
|
URL |
https://arxiv.org/abs/1701.05503 |
Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на эту карточку |
https://repository.kpfu.ru/?p_id=170473 |
Полная запись метаданных |
Поле DC |
Значение |
Язык |
dc.contributor.author |
Котов Николай Викторович |
ru_RU |
dc.contributor.author |
Салахиева Диана Витальевна |
ru_RU |
dc.contributor.author |
I. I Sadreev , Michael Z, Q Chen , Yoshinori Umezawa , Claudia Kemper, Gavin I Welsh Ildar I |
ru_RU |
dc.date.accessioned |
2017-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2017-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2017 |
ru_RU |
dc.identifier.citation |
Ildar I Sadreev, The competitive nature of STAT complex formation drives phenotype switching of T cells /Ildar I Sadreev, Michael Z Q Chen, Yoshinori Umezawa, Vadim N Biktashev, Claudia Kemper, Diana V Salakhieva, Gavin I Welsh, Nikolay V Kotov.-2017.-Cite as: arXiv:1701.05503 [q-bio.MN] |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/?p_id=170473 |
ru_RU |
dc.description.abstract |
IMMUNOLOGY |
ru_RU |
dc.description.abstract |
Signal transducers and activators of transcription (STATs) are key molecular determinants of T cell fate and effector function. A number of inflammatory diseases are characterized by an altered balance of T cell phenotypes and cytokine secretion. STATs, therefore, represent viable therapeutic targets in numerous pathologies. However, the underlying mechanisms of how the same STAT proteins regulate both the development of different T cell phenotypes and their plasticity during changes in extracellular conditions remain unclear. In this study, we investigated the STAT mediated regulation of T cell phenotype formation and plasticity using mathematical modeling and experimental data for intracellular STAT signaling proteins. The close fit of our model predictions to the experimental data for IFN-{\gamma} to IL-10 switching allows us to propose a potential mechanism for T cell switching that regulates human Th1/Tr1 responses. According to this mechanism, T cell phenotype switching is due to |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
Quantitative Biology |
ru_RU |
dc.subject |
Molecular Networks |
ru_RU |
dc.title |
The competitive nature of STAT complex formation drives phenotype switching of T cells |
ru_RU |
dc.type |
Статьи в зарубежных журналах и сборниках |
ru_RU |
|