Buszewska Małgorzata Eliza, Strzelecka-Kiliszek Agnieszka, Tylki-Szymańska Anna, Bandorowicz-Pikuła Joanna
Institut Biologii Doświadczalnej PAN im. Marcelego Nenckiego w Warszawie.
Postepy Biochem. 2007;53(2):169-73.
Niemann-Pick disease is a genetic disorder, affecting approximately 1 to 150,000 living births per year; in Poland 1-5 cases. Usually diagnosed in the childhood, Niemann-Pick disease results in death in the teenage years. Niemann-Pick disease is defined as a lysosomal storage disorder and is related to impaired transport and/or accumulation of specific lipids inside the cell. In this report, we provide evidence about potential role of annexins, calcium- and membrane-binding proteins, in the formation and stabilization of cholesterol-rich microdomains and their possible function in organizing the membranes of early and late endosomes, organelles affected in the type C Niemann-Pick disease characterized by abnormal accumulation of cholesterol and glycosphingolipids in lysosomal like organelles.
尼曼-皮克病是一种遗传性疾病,每年每15万例活产中约有1例受影响;在波兰,每年有1至5例。尼曼-皮克病通常在儿童期被诊断出来,患者多在青少年时期死亡。尼曼-皮克病被定义为一种溶酶体贮积症,与细胞内特定脂质的转运受损和/或积累有关。在本报告中,我们提供了关于膜联蛋白(钙和膜结合蛋白)在富含胆固醇的微结构域形成和稳定中的潜在作用的证据,以及它们在组织早期和晚期内体膜方面可能发挥的功能,尼曼-皮克C型疾病中受影响的细胞器,其特征是在溶酶体样细胞器中胆固醇和糖鞘脂异常积累。