Mitochondrial respiratory capacity is a critical regulator of CD8+ T cell memory development.

Mitochondrial respiratory capacity is a critical regulator of CD8+ T cell memory development.
复制标题

DOI:
10.1016/j.immuni.2011.12.007
复制
发表时间:
2012-01-27
期刊:
影响因子:
32.4
通讯作者:
Pearce EL
Pearce EL
中科院分区:
医学1区
文献类型:
--
作者:
van der Windt GJ;Everts B;Chang CH;Curtis JD;Freitas TC;Amiel E;Pearce EJ;Pearce EL

文献摘要

参考文献

被引文献

相似文献

CD8+ T细胞在激活后发生了重大的代谢变化,但代谢如何影响感染后长寿命记忆T (TM)细胞的建立仍然是一个关键问题。我们在这里表明,CD8+ TM细胞,而不是效应CD8+ (TE)细胞,具有大量的线粒体备用呼吸能力(SRC)。SRC是细胞在应对压力或工作增加时产生能量的额外能力,因此与细胞存活有关。我们发现白细胞介素-15 (IL-15)是一种对CD8+ TM细胞至关重要的细胞因子,通过促进线粒体生物发生和肉碱棕榈酰转移酶(CPT1a)的表达来调节SRC和氧化代谢,CPT1a是一种控制线粒体脂肪酸氧化(FAO)限速步骤的代谢酶。这些结果表明细胞因子如何通过调节线粒体代谢来控制感染后TM细胞的生物能量稳定性。
CD8+ T cells undergo major metabolic changes upon activation, but how metabolism influences the establishment of long-lived memory T (TM) cells after infection remains a key question. We have shown here that CD8+ TM cells, but not effector CD8+ (TE) cells, possessed substantial mitochondrial spare respiratory capacity (SRC). SRC is the extra capacity available in cells to produce energy in response to increased stress or work and as such is associated with cellular survival. We found that interleukin-15 (IL-15), a cytokine critical for CD8+ TM cells, regulated SRC and oxidative metabolism by promoting mitochondrial biogenesis and expression of carnitine palmitoyl transferase (CPT1a), a metabolic enzyme that controls the rate-limiting step to mitochondrial fatty acid oxidation (FAO). These results show how cytokines control the bioenergetic stability of TM cells after infection by regulating mitochondrial metabolism.
DOI: 10.1021/ac900881z
发表时间: 2009-08-15
影响因子: 7.4
作者:
Gerencser, Akos A.;Neilson, Andy;Choi, Sung W.;Edman, Ursula;Yadava, Nagendra;Oh, Richard J.;Ferrick, David A.;Nicholls, David G.;Brand, Martin D.
通讯作者: Brand, Martin D.
DOI: 10.1038/ni1009
发表时间: 2003-12-01
期刊: NATURE IMMUNOLOGY
影响因子: 30.5
作者:
Kaech, SM;Tan, JT;Ahmed, R
通讯作者: Ahmed, R
DOI: 10.3791/2511
发表时间: 2010-12-06
期刊: Journal of visualized experiments : JoVE
影响因子: --
作者:
Nicholls, David G;Darley-Usmar, Victor M;Ferrick, David A
通讯作者: Ferrick, David A
DOI: 10.1084/jem.191.5.771
发表时间: 2000-03-06
期刊: The Journal of experimental medicine
影响因子: --
作者:
Kennedy MK;Glaccum M;Brown SN;Butz EA;Viney JL;Embers M;Matsuki N;Charrier K;Sedger L;Willis CR;Brasel K;Morrissey PJ;Stocking K;Schuh JC;Joyce S;Peschon JJ
通讯作者: Peschon JJ
DOI: 10.1111/j.1471-4159.2009.06055.x
发表时间: 2009-05
影响因子: 4.7
作者:
Choi SW;Gerencser AA;Nicholls DG
通讯作者: Nicholls DG