JN-NPC1²¡µÄµÚÒ»¸öKnock-inСÊóÄ£×Ó
ÔÚ×îеÄÒ»ÆÚJNÉÏ£¬Ò»ÏîÑо¿¹¹½¨ÁËNPC²¡µÄСÊóKnock-inÄ£×Ó£¬¸ÃÄ£×Ó¾ßÓÐÀàËÆÈËÀàNPC1²¡µÄ±íÐÍ£¬¿ÉÒÔÓÃÓÚ¾ÙÐÐÁÙ´²Ç°µÄÒ©ÎïÊÔÑé¡£

ƾ֤WikiÉϵÄÚ¹ÊÍ£ºNiemann¨CPick type C is a lysosomal storage disease associated with mutations in NPC1 and NPC2 genes. Niemann¨CPick type C strikes an estimated 1:150,000 people.Approximately 50% of cases present before 10 years of age, but manifestations may first be recognized as late as the sixth decade.
ÏêϸµÄ»úÖÆÊÇ£ºThe NPC1 gene encodes a protein that is located in membranes inside the cell and is involved in the movement of cholesterol and lipids within cells.A deficiency of this protein leads to the abnormal build up of lipids and cholesterol within cell membranes.
ÏêϸÄÚÈÝÔڴ˲»×öÏêÊö¡£

С±àÆÀÓÕâ¸ö²¡µÄÑо¿ÊÇÈ«ÇòÈÈÃÅ£¬ÏÖÔÚÈ«ÌìÏ»¹Ã»ÓкõÄÖÎÁÆÒªÁì¡£Õâ¸ö¼²²¡ÊÇÈÜøÌåÖü»ýÖ¢ÖеÄÒ»ÖÖ£¬ÓÉÓÚNPC1»ùÒòµÄÍ»±äµ¼ÖµĴó×ڵĵ¨¹Ì´¼ºÍÇÊÁ×Ö¬ÔÚÈÜøÌåÖÐȺ¼¯¡£¼ÈÍùµÄNPC1СÊóÄ£×ÓÖ÷ÒªÊǽ«NPC1»ùÒòÇóý£¬¿ÉÊÇûÓÐÁËNPC1ÂѰ׵ıí´ï£¬ÕâÑùµÄ»°£¬Ñо¿Ö°Ô±¾ÍÎÞ·¨Æ¾Ö¤ÂѰ×ÎÈ̬µÄ»úÖÆ¶ÔÕâ¸ö¼²²¡¾ÙÐиÉÔ¤Ñо¿¡£ÎªÁ˱í´ïÕâ¸öÂѰף¬¿ÉÊÇÓÖҪģÄâ³ö¼²²¡µÄ±íÐÍ£¬Ö±½ÓµÄÒ»ÖÖ·½·¨£¬¾ÍÊǽ«ÈËÀàÖеÄÍ»±ä»ùÒòÖ±½ÓÔØÈëСÊóµÄ»ùÒò×éÖУ¬¹¹½¨Knock-inÄ£×Ó¡£ËûÃÇ·¢Ã÷£¬Õâ¸öKIСÊó¼òÖ±ÌåÏÖ³öÁËÀàËÆÓÚÈËÀàNPC1µÄ¼²²¡±íÐÍ£¬²¢ÇÒʹÓÃ×éÂѰ×È¥ÒÒõ£»¯Ã¸µÄÒÖÖÆ¼Á¼òÖ±¿ÉÒÔÎȹ̸ÃÂѰ׵Ľṹ¡£ÕâÌáÐÑproteostaticµÄÒªÁì¿ÉÒÔÓÃÓÚÔöÌíÍ»±äNPC1µÄ½á¹¹£¬ÔöÌíËûµÄ°ëË¥ÆÚ£¬Î¬³ÖÆäÉúÎïѧ¹¦Ð§£¬»òÔÊÐíÒÔÓÃÓڸò¡µÄÖÎÁÆ¡£

·ÖÏíµ½£º