T Cells in G sub(1) Provide a Memory-Like Response to Secondary Stimulation
The commitment of naive T cells to proliferate is a function of the strength and duration of stimuli mediated by the TCR and coreceptors. Ranges of 2-20 h of stimulation have been reported as necessary in vitro. Whether T cells actually experience uninterrupted stimulation for such long periods unde...
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Published in | The Journal of immunology (1950) Vol. 174; no. 7; pp. 4010 - 4018 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
01.04.2005
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Online Access | Get full text |
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Summary: | The commitment of naive T cells to proliferate is a function of the strength and duration of stimuli mediated by the TCR and coreceptors. Ranges of 2-20 h of stimulation have been reported as necessary in vitro. Whether T cells actually experience uninterrupted stimulation for such long periods under physiological conditions is controversial. Here we ask whether commitment to proliferate requires continuous stimulation, or can T cells integrate intermittent periods of stimulation. T cells were stimulated for two short-term (subthreshold) periods (5-7 h) either sequentially or separated by an interval of rest. Naive lymph node T cells were able to integrate interrupted stimulation, even when the duration of rest was as long as 2 days. Furthermore, when short-term-stimulated T cells were separated by density, three populations were observed: low density blasts, intermediate density G sub(1) cells, and high density G sub(0) cells. Low density cells progressed to division without further stimulation, whereas G sub(0) and G sub(1) cells remained undivided. However, after a period of rest, a second subthreshold stimulation caused the G sub(1) but not the G sub(0) fraction to quickly proceed through the cell cycle. We conclude that noncycling T cells in the G sub(1) phase of the cell cycle remain in a state of readiness for prolonged periods of time, and may represent a population of memory-like effectors capable of responding rapidly to antigenic challenge. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 0022-1767 |