Liscum Laura, Sturley Stephen L
Department of Physiology, Tufts University School of Medicine, 136 Harrison Avenue, Boston, MA 02111, USA.
Biochim Biophys Acta. 2004 Oct 11;1685(1-3):22-7. doi: 10.1016/j.bbalip.2004.08.008.
Niemann-Pick C 1 (NPC1) is a large integral membrane glycoprotein that resides in late endosomes, whereas NPC2 is a small soluble protein found in the lumen of lysosomes. Mutations in either NPC1 or NPC2 result in aberrant lipid transport from endocytic compartments, which results in lysosomal storage of a complex mixture of lipids, primarily cholesterol and glycosphingolipids. What are the biological functions of the NPC1 and NPC2 proteins? Here we review what is known about the intracellular itinerary of these two proteins as they facilitate lipid transport. We propose that the intracellular trafficking patterns of these proteins will provide clues about their function.
尼曼-皮克C1(NPC1)是一种驻留在晚期内体中的大型整合膜糖蛋白,而NPC2是一种存在于溶酶体腔内的小的可溶性蛋白。NPC1或NPC2中的突变会导致从内吞区室的异常脂质转运,这会导致脂质(主要是胆固醇和糖鞘脂)的复杂混合物在溶酶体中储存。NPC1和NPC2蛋白的生物学功能是什么?在这里,我们综述了关于这两种蛋白在促进脂质转运时的细胞内行程的已知信息。我们提出,这些蛋白的细胞内运输模式将为它们的功能提供线索。