Ultrastructural alterations in the optic nerve in transmissible spongiform encephalopathies or prion diseases--a review.
نویسندگان
چکیده
The involvement of the visual system is well recognised in TSEs. The present review summarises the ultrastructural changes in the optic nerves in experimental infections of laboratory rodents with the agents of two human TSEs (CJD and GSS) and with two isolates of the scrapie agent. Vacuoles of myelinated fibres were found within myelin sheaths and themselves contained secondary vacuoles (vacuoles within other vacuoles) and curled membrane fragments not unlike the vacuoles in cerebral grey matter (see also: Spongiform change--an electron microscopic view; this issue). The myelin sheath had split either at the major dense line or at the intraperiod line. In addition, axons contained vacuoles within the axoplasm, corresponding to the typical spongiform vacuoles of grey matter. Vacuolation of myelinated fibres was accompanied by an exuberant cellular reaction consisting of macrophages containing numerous mitochondria, abundant rough endoplasmic reticulum and secondary lysosomes filled with digested myelin debris, electron-dense material and sometimes entire myelin-bounded vacuoles. Within macrophages myelin fragments undergoing active digestion were often seen, together with lyre-like bodies and paracrystalline inclusions. Astrocytes and their processes were prominent and glial filaments and many mitochondria were readily detected. Proliferation of the inner mesaxons was also seen. Cross-sectional profiles of many myelinated fibres contained membranous organelles continuous with the inner lamellae of the oligodendroglial cells. The inner mesaxon proliferations formed whorls and loops. In some axons proliferation was so severe that the mesaxonal loops filled the whole cross-section of the axon. Occasionally there was intrusion of the membranous tongue of the inner mesaxon into the axoplasm. Dystrophic neurites were relatively numerous. In GSS-infected animals some axons underwent demyelination with stripping of the myelin lamellae, while still others underwent vesicular myelin degeneration. It is of special note that in the cytoplasm of several cells as well as the axoplasm numerous autophagic vacuoles were seen.
منابع مشابه
An outline of the neuropathology of transmissible spongiform encephalopathies (prion diseases).
We review here the basic neuropathology of transmissible spongiform encephalopathies (TSE) or prion diseases. The classic hallmark of TSE neuropathology is a combination (in different proportions in different diseases) of spongiform change, astrocytosis, neuronal loss and amyloid plaques. Immunohistochemically, accumulation of the abnormal isoform of prion protein (PrP(sc) or PrP(d)) is regarde...
متن کاملMolecular mechanisms of neurodegeneration mediated by dysfunctional subcellular organelles in transmissible spongiform encephalopathies.
Transmissible spongiform encephalopathies refer to a group of infectious neurodegenerative diseases with an entirely novel mechanism of transmission and pathophysiology including synaptic damage, dendritic atrophy, vacuolization, and microglial activation. Extensive neuronal loss is the main cause of chronic brain deterioration and fatal outcome of prion diseases. As the final outcome of pathol...
متن کاملVisual pathology in animal prion diseases.
Prion diseases, also known as the transmissible spongiform encephalopathies (TSEs), are a group of slowly developing neurodegenerations occurring in human and animals. Prion diseases can be transferred between animals, humans, from humans to animals, and from animals to humans. As a result, the central nervous system is attacked, resulting in microglia activation, astrocytosis, prion plaque dep...
متن کاملCell death and autophagy in prion diseases (transmissible spongiform encephalopathies).
Neuronal autophagy, like apoptosis, is one of the mechanisms of programmed cell death. In this review, we summarize current information about autophagy in naturally occurring and experimentally induced scrapie, Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker syndrome against the broad background of neural degenerations in transmissible spongiform encephalopathies (TSEs). Typically ...
متن کاملPrP genetics in ruminant transmissible spongiform encephalopathies.
Scrapie, bovine spongiform encephalopathy (BSE), and chronic wasting disease (CWD) are prion diseases in ruminants with considerable impact on animal health and welfare. They can also pose a risk to human health and control is therefore an important issue. Prion protein (PrP) genetics may be used to control and eventually eradicate animal prion diseases. The PrP gene in sheep and other represen...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Folia neuropathologica
دوره 42 Suppl B شماره
صفحات -
تاریخ انتشار 2004