Patel Vimal A, Longacre-Antoni Angelika, Cvetanovic Marija, Lee Daniel J, Feng Lanfei, Fan Hanli, Rauch Joyce, Ucker David S, Levine Jerrold S
Division of Nephrology, Department of Medicine, University of Illinois at Chicago, IL 60612, USA.
Autoimmunity. 2007 Jun;40(4):274-80. doi: 10.1080/08916930701357463.
Growing evidence exists for a new role for apoptotic cell recognition and clearance in immune homeostasis. Apoptotic cells at all stages, irrespective of membrane integrity, elicit a signature set of signaling events in responding phagocytes, both professional and non-professional. These signaling events are initiated by receptor-mediated recognition of apoptotic determinants, independently of species, cell type, or apoptotic stimulus. We propose that the ability of phagocytes to respond to apoptotic targets with a characteristic set of signaling events comprises a second distinct dimension of innate immunity, as opposed to the traditional innate discrimination of self vs. non-self. We further propose that a loss or abnormality of the signaling events elicited by apoptotic cells, as distinct from the actual clearance of those cells, may predispose to autoimmunity.
越来越多的证据表明,凋亡细胞的识别和清除在免疫稳态中具有新的作用。各个阶段的凋亡细胞,无论膜完整性如何,都会在专业和非专业的吞噬细胞中引发一组标志性的信号事件。这些信号事件由受体介导的凋亡决定簇识别引发,与物种、细胞类型或凋亡刺激无关。我们提出,吞噬细胞以一组特征性信号事件对凋亡靶标作出反应的能力构成了固有免疫的第二个不同维度,这与传统的自身与非自身的固有区分不同。我们进一步提出,凋亡细胞引发的信号事件的丧失或异常,与这些细胞的实际清除不同,可能易患自身免疫性疾病。