[Annexins in Niemann-Pick type C disease].
Małgorzata Eliza Buszewska, Agnieszka Strzelecka‐Kiliszek, Anna Tylki‐Szymańska, Joanna Bandorowicz‐Pikuła
Abstract
Małgorzata Eliza Buszewska, Agnieszka Strzelecka‐Kiliszek, Anna Tylki‐Szymańska, Joanna Bandorowicz‐Pikuła
Abstract
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.
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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.
Key concepts: Niemann–Pick disease, Niemann–Pick disease, type C, Endosome, NPC1, Organelle, Lysosome, Disease, Cholesterol