Not just amyloid: physiological functions of the amyloid precursor protein family

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作者
Ulrike C. Müller
Thomas Deller
Martin Korte
机构
[1] Ruprecht-Karls University Heidelberg,
[2] Institute of Pharmacy and Molecular Biotechnology,undefined
[3] Bioinformatics and Functional Genomics,undefined
[4] Goethe University Frankfurt,undefined
[5] Institute of Clinical Neuroanatomy,undefined
[6] Neuroscience Center,undefined
[7] TU Braunschweig,undefined
[8] Zoological Institute,undefined
[9] Cellular Neurobiology,undefined
[10] Helmholtz Centre for Infection Research,undefined
[11] Neuroinflammation and Neurodegeneration Group,undefined
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摘要
Amyloid precursor protein (APP) and the APP-like proteins APLP1 and APLP2 form the mammalian APP gene family. They have important physiological functions in the peripheral and central nervous systems, some of which are still emerging.APP family members share a similar structure and have partially overlapping functions. Their processing by canonical and non-canonical secretases results in numerous biologically active fragments, which mediate distinct and even opposing functions.Membrane-bound APP family members interact in cis or in trans, which enables them to function as cell-adhesion molecules. Large numbers of extracellular and intracellular binding partners have been identified, and this Review summarizes those that are involved in physiological pathways in vivo.Biological functions in which APP family members are involved include nervous system development, the formation and function of the neuromuscular junction, synaptogenesis, dendritic complexity and spine density, axonal growth and guidance, and synaptic functions, including synaptic plasticity, learning and memory.α-Secretase cleavage of APP releases the neuroprotective and neurotrophic fragment APPsα. It upregulates protective pathways, inhibits neuronal apoptosis, increases neuronal resistance to brain injuries and has a crucial role in synaptic plasticity, learning and memory.Increasing APPsα levels may be of therapeutic value. Pharmacotherapeutic and gene-therapeutic approaches could complement amyloid-targeting strategies.
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页码:281 / 298
页数:17
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