Prions Some Physiological and Pathophysiological Aspects
The cellular prion protein (PrPC) is expressed as a cell surface protein mainly in the central and peripheral nervous system. The discovery that prions are infectious agents changed the concept of protein synthesis in modern biology and built a bridge between the genesis of infectious and genetic di...
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Format: | Electronic Book Chapter |
Language: | English |
Published: |
IntechOpen
2019
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Subjects: | |
Online Access: | DOAB: download the publication DOAB: description of the publication |
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Summary: | The cellular prion protein (PrPC) is expressed as a cell surface protein mainly in the central and peripheral nervous system. The discovery that prions are infectious agents changed the concept of protein synthesis in modern biology and built a bridge between the genesis of infectious and genetic diseases. This book discusses the normal function of the PrPC and its modulatory role in synaptic mechanisms. It describes the pathophysiological processes that accompany TSE - neurotoxicity, loss of anti-inflammatory protective function, neuronal death including prion-induced autophagy and apoptosis, and accumulation of PrPSc in the cytoplasm of neurons. Another aspect outlined here is that some prion diseases show strain variations that determine their development, demonstrating their key role in the development and progression of TSE. |
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Physical Description: | 1 electronic resource (82 p.) |
ISBN: | intechopen.74080 9781789850185 9781789850178 9781838817688 |
Access: | Open Access |