Journal of immunology (Baltimore, Md. : 1950) · 2013
Cutting edge: The signals for the generation of T cell memory are qualitatively different depending on TCR ligand strength.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Knudson Karin M, Hamilton Sara E, Daniels Mark A, Jameson Stephen C, Teixeiro Emma
Аннотация
CD8 T cell memory critically contributes to long-term immunity. Both low- and high-affinity TCR signals are able to support the differentiation of memory CD8 T cells. However, it is unclear whether the requirements for memory development change when TCR signal strength is altered. To gain further insight into this question, we used a TCRβ transmembrane domain mutant model that is defective in the generation of memory in response to high-affinity ligands. Surprisingly, lowering TCR signal strength, by stimulation with low-affinity ligands, resulted in normal memory development. Restoration of memory correlated with recovery of TCR-dependent NF-κB signaling. Thus, these data provide novel evidence that the requirements for memory are qualitatively different depending on TCR signal strength.
Предметные рубрики MeSH
Active Transport, Cell NucleusAdoptive TransferAnimalsAntigensCD8-Positive T-LymphocytesGene Expression RegulationImmunologic MemoryImmunomagnetic SeparationLigandsListeria monocytogenesListeriosisLymphocyte CountLymphopeniaLymphopoiesisMiceMice, CongenicMice, Inbred C57BLMice, TransgenicNF-kappa BOvalbuminPeptide FragmentsPoint MutationProtein Structure, TertiaryReceptors, Antigen, T-Cell, alpha-betaT-Lymphocyte Subsets