Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P62988 (
Ubiquitin
)
4,326
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Serial sections of formalin-fixed, paraffin-embedded muscle biopsy specimens from 28 Quarter Horse, Paint, and draft-related breeds, aged 0.5-23 years, were treated with periodic acid-Schiff (PAS) stain for glycogen and were immunostained to detect ubiquitin expression. On the basis of findings in PAS-stained sections, a diagnosis of equine polysaccharide storage myopathy (EPSSM) was made in 22 horses aged 2-23 years (mean, 9.4 years); samples from 6 horses aged 0.5-15 years (mean, 7.3 years) had a normal PAS staining pattern, with no relevant lesions.
Ubiquitin
expression was detected in all but a 2-year-old EPSSM-affected horse and was not detected in the non-EPSSM-affected horses.
Ubiquitin
expression was greater than the degree of PAS-positive,
amylase
-resistant material, and ubiquitin was detected in aggregates of
amylase
-sensitive glycogen as well as in aggregates of
amylase
-resistant material. Results suggest that glycogen aggregates develop and are ubiquitinated prior to development of
amylase
-resistant inclusions.
Ubiquitin
immunostaining may be most useful for confirming the diagnosis of EPSSM in horses with only
amylase
-sensitive glycogen aggregates and in horses with early
amylase
-resistant inclusions. However, ubiquitin immunostaining is no more sensitive than is PAS staining for diagnosis of EPSSM.
...
PMID:Ubiquitin expression in muscle from horses with polysaccharide storage myopathy. 1667 73
Muscle samples from 24 horses with polysaccharide storage myopathy were stained with periodic acid-Schiff (PAS) stain and were immunostained for ubiquitin. Abnormalities detected with PAS stain were coarse granular cytoplasmic aggregates of
amylase
sensitive glycogen, subsarcolemmal aggregates of glycogen, central
amylase
sensitive bodies, and a variety of subsarcolemmal to intracytoplasmic
amylase
resistant polyglucosan inclusions. All
amylase
resistant inclusions were positive for ubiquitin.
Ubiquitin
was also detected in many
amylase
sensitive inclusions. Based on morphologic findings and pattern of ubiquitin staining, a sequence of events, beginning with abnormal glycogen storage followed by ubiquitination and eventual development of
amylase
resistance, is proposed.
...
PMID:Development of polyglucosan inclusions in skeletal muscle. 1691 52