Lewy body

Photomicrographs of regions of substantia nigra in this Parkinson's patient show Lewy bodies and Lewy neurites in various magnifications. Top panels show a 60× magnification of the alpha-synuclein intraneuronal inclusions aggregated to form Lewy bodies. The bottom panels are 20× magnification images that show strand-like Lewy neurites and rounded Lewy bodies of various sizes. Neuromelanin-laden cells of the substantia nigra are visible in the background. Stains used: mouse monoclonal alpha-synuclein antibody; counterstained with Mayer's haematoxylin
Lewy bodies

Lewy bodies are the inclusion bodies – abnormal aggregations of protein – that develop inside nerve cells affected by Parkinson's disease (PD), the Lewy body dementias (Parkinson's disease dementia and dementia with Lewy bodies), and some other disorders. They are also seen in cases of multiple system atrophy, particularly the parkinsonian variant (MSA-P).[1]

They are identified in tissue examined under the microscope. Infrared microspectroscopy has been used to distinguish dementia with Lewy bodies (DLB) from Alzheimer’s, which are sometimes misdiagnosed as the other.[2] With this method, white blood cells and plasma can be looked at under the microscope, and compared through machine learning, to see whether there is a Lewy body buildup causing DLB.[2] DLB can also be tested for using MRI, PET, CT, and CT scanning.[2]

Lewy bodies appear as spherical masses in the cytoplasm that displace other cell components. For instance, some Lewy bodies tend to displace the nucleus to one side of the cell.[3] There are two main kinds of Lewy bodies: classical and cortical. Lewy bodies may be found in the midbrain (within the substantia nigra) or within the cortex. A classical Lewy body is an eosinophilic cytoplasmic inclusion consisting of a dense core surrounded by a halo of 10-nm-wide radiating fibrils, the primary structural component of which is alpha-synuclein. Cortical Lewy bodies are also composed of alpha-synuclein fibrils, but are less defined and lack halos. This kind of Lewy body is one of those aforementioned that regularly displaces the nucleus.[3] In histopathology, cortical Lewy bodies are a distinguishing feature for dementia with Lewy bodies, but may occasionally be seen in ballooned neurons characteristic of behavioural variant frontotemporal dementia and corticobasal degeneration,[4] as well as in patients with other tauopathies.[5]

History

In 1910, Fritz Heinrich Lewy was studying in Berlin for his doctorate.[6] He was the first doctor to notice some unusual proteins in the brain make some people act and think differently, but as of that time, scientists had not been able to determine the purpose of these proteins. Some common behavioral changes that occur with Lewy body dementia, and can be relatively easy to observe externally, include: forgetfulness, being less able to focus, agitation, aggression, and being extra tired in the daytime.[7] His discovery became known as Lewy bodies, as published in the Handbook of Neurology in 1912 by Max Lewandowsky,[7] comparing them to earlier findings by Gonzalo Rodríguez Lafora.[8] In 1913, Lafora described another case, and acknowledged Lewy as the discoverer, naming them cuerpos intracelulares de Lewy (intracellular Lewy bodies).[8] Konstantin Nikolaevich Trétiakoff found them in 1919 in the substantia nigra of PD brains, called them corps de Lewy and is credited with the eponym.[8] In 1923, Lewy published his findings in a book, The Study on Muscle Tone and Movement. Including Systematic Investigations on the Clinic, Physiology, Pathology, and Pathogenesis of Paralysis agitans.[9] Eliasz Engelhardt, who is in the neurology department at Federal University of Rio de Janeiro, argued in 2017 that Lafora should be credited with the eponym, because he named them six years before Trétiakoff.[8] Nonetheless, Trétiakoff is still the primary figure acknowledged for coining the term, “Lewy bodies.”[8]

According to the Journal of the History of the Neurosciences, Dr. Lewy became interested in studying more about the brain (neurology), because of the discovery that Alois Alzheimer made in 1906. The article mentions that the third reported case of Alzheimer's disease had histological structures that happened to be similar to Lewy body histology slides, but the contribution was not given to Lewy's finding.[10]

Cell biology

Photomicrograph of the dorsal motor nucleus of the vagus nerve (DmX) in a transverse section along the upper medulla shown to be affected by the abnormally deposited alpha synuclein as part of intraneuronal Lewy bodies found (extreme right): DmX is one of the earliest sites affected by synuclein deposition in Parkinson's disease.[11]

A Lewy body is composed of the protein alpha-synuclein associated with other proteins, such as ubiquitin,[12] neurofilament protein, and alpha B crystallin. Tau proteins may also be present, and Lewy bodies may occasionally be surrounded by neurofibrillary tangles.[13][14] Lewy bodies and neurofibrillary tangles can occasionally exist in the same neuron, particularly in the amygdala.[15]

Alpha-synuclein modulates DNA repair processes, including repair of DNA double-strand breaks (DSBs) by the process of non-homologous end joining[16] The repair function of alpha-synuclein appears to be greatly reduced in Lewy body bearing neurons, and this reduction may trigger cell death. Mutations are the reason behind their damaged repair function.[17] One mutation in particular, in the gene encoding for presynaptic alpha-synuclein, was found to have been passed down from family members with PD.[17] Similarly in regards to DLB, Lewy bodies retrieved from DLB brains were found to contain alpha-synuclein proteins that were shortened by mutations.[17] This shows how mutated alpha-synuclein was found in Lewy body-associated diseases, both when looking at family pedigrees and directly at individual brainstems.

Lewy bodies are believed to represent an aggresome response in the cell.[18] When misfolded proteins aggregate, or clump together, many diseases are more likely to develop, including those that are associated with Lewy bodies.[19] Aggregation is believed to occur when there is a high amount of misfolded proteins in the ubiquitin-proteasome pathway, which are then brought to a resulting aggresome so they can be organized into one place.[19] Since Lewy bodies are made of ubiquitinated proteins that would be handled in the ubiquitin-proteasome pathway, they may be made from this or a similar process if the pathway capacity is indeed exceeded by misfolded proteins that aggregate together.[19] Accordingly, the aggresome, where the damaged proteins fully aggregate, is akin to the Lewy body.

Despite their differences, there is evidence that a particular protein family, called 14-3-3, plays a role in the formation of both cortical and classical Lewy bodies.[20] This makes it an important protein family in regards to Lewy body-associated diseases, and there are at least 7 forms of it that have been clearly identified in mammals.[20]

Lewy neurites

Lewy neurites in a DLB case. Stain application: immunohistochemical

Lewy neurites are abnormal neurites in diseased neurons, containing granular material and abnormal α-synuclein filaments similar to those found in Lewy bodies.[21] Like Lewy bodies, Lewy neurites are a feature of α-synucleinopathies such as dementia with Lewy bodies, Parkinson's disease, and multiple system atrophy.[22] They are also found in the CA2-3 region of the hippocampus in Alzheimer's disease.[22] Although they have similar functions and effects to Lewy bodies, they have some clear differences in their appearances. [23] Both have a three-layered internal structure, but of different sizes.[23] The visible differences between them suggest that Lewy neurites structurally evolve into Lewy bodies, potentially when the neurites extend into the cell soma.[23] There is still not enough research to confirm this, but if confirmed, it would mean that Lewy neurites and Lewy bodies are made from the same mechanism.[23] This makes Lewy neurites important to research when considering Lewy body-associated diseases, considering that if they do evolve into Lewy bodies, then they would therefore also be associated with the same diseases.

See also

References

  1. Jellinger KA (September 2007). "More frequent Lewy bodies but less frequent Alzheimer-type lesions in multiple system atrophy as compared to age-matched control brains". Acta Neuropathologica. 114 (3): 299–303. doi:10.1007/s00401-007-0227-4. PMID 17476513. S2CID 32406286.
  2. 1 2 3 Salman A, Lapidot I, Shufan E, Agbaria AH, Porat Katz BS, Mordechai S (April 2020). "Potential of infrared microscopy to differentiate between dementia with Lewy bodies and Alzheimer's diseases using peripheral blood samples and machine learning algorithms". Journal of Biomedical Optics. 25 (4): 1–15. doi:10.1117/1.JBO.25.4.046501. PMC 7177186. PMID 32329265.
  3. 1 2 Spillantini MG, Schmidt ML, Lee VM, Trojanowski JQ, Jakes R, Goedert M (August 1997). "Alpha-synuclein in Lewy bodies". Nature. 388 (6645): 839–840. doi:10.1038/42166. PMID 9278044.
  4. Dickson DW, Feany MB, Yen SH, Mattiace LA, Davies P (1996). "Cytoskeletal pathology in non-Alzheimer degenerative dementia: new lesions in diffuse Lewy body disease, Pick's disease, and corticobasal degeneration". Journal of Neural Transmission. Supplementum. Journal of Neural Transmission Supplement. 47: 31–46. doi:10.1007/978-3-7091-6892-9_2. ISBN 978-3211828236. PMID 8841955.
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