Simister N E, Jacobowitz Israel E, Ahouse J C, Story C M
Rosenstiel Center for Basic Biomedical Sciences, W. M. Keck Institute for Cellular Visualization, Waltham, MA, USA.
Biochem Soc Trans. 1997 May;25(2):481-6. doi: 10.1042/bst0250481.
FcRn was originally identified as the receptor responsible for IgG binding to the intestinal epithelium of neonatal rats and mice. FcRn transports IgG from milk across the intestinal epithelial cells of the suckling animal. Subsequently, FcRn was detected in tissues involved in the transmission of IgG from mother to fetus: rat fetal yolk sac, mouse fetal yolk sac and human placental syncytiotrophoblast. In addition, FcRn mRNA has been detected in many tissues of adult rats, mice and humans, and FcRn is present in several adult tissues and in cell lines. The selective protection from catabolism of IgG compared with other immunoglobulins is lost in mice that lack functional FcRn. One function of FcRn in tissues that do not transport IgG, and beyond the perinatal period, is thus to rescue circulating IgG from degradation. These recent observations reveal a more widespread use of FcRn than had been supposed.
FcRn最初被鉴定为负责IgG与新生大鼠和小鼠肠道上皮结合的受体。FcRn将乳汁中的IgG转运过哺乳期动物的肠道上皮细胞。随后,在参与IgG从母体向胎儿传递的组织中检测到了FcRn:大鼠胎儿卵黄囊、小鼠胎儿卵黄囊和人胎盘合体滋养层。此外,在成年大鼠、小鼠和人类的许多组织中都检测到了FcRn mRNA,并且FcRn存在于几种成年组织和细胞系中。与其他免疫球蛋白相比,缺乏功能性FcRn的小鼠丧失了对IgG分解代谢的选择性保护。因此,FcRn在不转运IgG的组织中以及围产期之后的一个功能是挽救循环中的IgG免于降解。这些最新观察结果表明FcRn的用途比之前认为的更为广泛。