Structural and functional alterations of the cell nucleus in skeletal muscle wasting: the evidence in situ
Author(s) -
Manuela Malatesta,
G. Meola
Publication year - 2010
Publication title -
european journal of histochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 42
eISSN - 2038-8306
pISSN - 1121-760X
DOI - 10.4081/ejh.2010.e44
Subject(s) - myotonic dystrophy , wasting , skeletal muscle , sarcopenia , biology , cell nucleus , microbiology and biotechnology , pathogenesis , phenotype , dystrophy , pathological , nucleus , rna splicing , pathology , rna , medicine , endocrinology , genetics , gene
The histochemical and ultrastructural analysis of the nuclear components involved in RNA transcription and splicing can reveal the occurrence of cellular dysfunctions eventually related to the onset of a pathological phenotype. In recent years, nuclear histochemistry at light and electron microscopy has increasingly been used to investigate the basic mechanisms of skeletal muscle diseases; the study in situ of nuclei of myofibres and satellite cells proved to be crucial for understanding the pathogenesis of skeletal muscle wasting in sarcopenia, myotonic dystrophy and laminopathies.
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