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Getting the measure of apoptosis.

机译:获得细胞凋亡的量度。

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摘要

Programmed cell death (PCD), or more particularly the mode of PCD termed apoptosis, entered the research mainstream in the early 1990s when immunologists began to realize the enormous impact that this mode of cell death had on all aspects of immunity, from selection of T- and B-lymphocytes during development, homeostatic control of mature lymphocyte populations, to the elimination of infected cells by cytotoxic lymphocytes, as well as in other settings. What followed from the mid-to-late 1990s was akin to a Klondike goldrush of new discoveries in the field, with significant advances in our understanding of the molecular control of apoptosis being made on an almost monthly basis. The pace of truly major advances in the cell-death field has inevitably slowed in recent years but these new advances are just as exciting as their predecessors, especially as new ground becomes increasingly harder to find. The consequences of all of this effort has been the discovery of many of the major molecular participantsin the cell-death machinery, from simple metazoans to mammals, and a fairly good understanding of how these molecules collaborate to eliminate cells in a diversity of settings [1-3].
机译:程序性细胞死亡(PCD),或更具体地说是称为凋亡的PCD模式,在1990年代初进入了研究主流,当时免疫学家开始从选择T到变体,意识到这种细胞死亡模式对免疫所有方面的巨大影响。 -和B淋巴细胞在发育过程中,对成熟淋巴细胞群体进行体内平衡控制,以消除细胞毒性淋巴细胞以及在其他环境中感染的细胞。从1990年代中后期开始,类似于该领域新发现的克朗代克(Klondike)淘金热,我们对细胞凋亡的分子控制的了解几乎每月都在取得重大进展。近年来,细胞死亡领域真正重大进展的步伐不可避免地放慢了脚步,但是这些新进展与其前辈一样令人兴奋,尤其是在新的领域越来越难找到的时候。所有这些努力的结果是发现了细胞死亡机制中的许多主要分子参与者,从简单的后生动物到哺乳动物,并且对这些分子如何协同作用以消除各种环境中的细胞有相当好的理解[1]。 -3]。

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