Journal article icon

Journal article

Tubular aggregates and cylindrical spirals have distinct immunohistochemical signatures

Abstract:
Tubular aggregates and cylindrical spirals are 2 distinct ultrastructural abnormalities observed in muscle biopsies that have similar histochemical staining characteristics on light microscopy. Both are found in a wide range of disorders. Recently, a number of genetic mutations have been reported in conditions with tubular aggregates in skeletal muscle. It is widely accepted that tubular aggregates arise from the sarcoplasmic reticulum, but the origin of cylindrical spirals has been less clearly defined. We describe the histopathological features of myopathies with tubular aggregates, including a detailed immunohistochemical analysis of congenital myasthenic syndromes with tubular aggregates due to mutations in GFPT1 and DPAGT1, and myopathies with cylindrical spirals. Our findings support the notion that cylindrical spirals, like tubular aggregates, derive primarily from the sarcoplasmic reticulum; however, immunohistochemistry indicates that different molecular components of the sarcoplasmic reticulum may be involved and can be used to distinguish between these different inclusions. The immunohistochemical differences may also help to guide genetic testing.
Publication status:
Published
Peer review status:
Peer reviewed

Actions


Access Document


Publisher copy:
10.1093/jnen/nlw096

Authors



More from this funder
Funding agency for:
Healy, E
Grant:
BRC128/NS/MH5992
More from this funder
Funding agency for:
Brady, S
Holton, J


Publisher:
Oxford University Press
Journal:
Journal of Neuropathology Experimental Neurology More from this journal
Volume:
75
Issue:
12
Pages:
1171-1178
Publication date:
2016-12-07
DOI:
EISSN:
1554-6578
ISSN:
0022-3069


Language:
English
Keywords:
Pubs id:
pubs:666556
UUID:
uuid:f6fba2c8-6255-4532-8e7a-e07c2a1386e1
Local pid:
pubs:666556
Source identifiers:
666556
Deposit date:
2017-06-14

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP