Publication: Morphological and biochemical patterns in skeletal muscle apoptosis
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Date
2010
Authors
D’Emilio, A. ; Biagiotti, L. ; Burattini, S. ; Battistelli, M. ; Canonico, B. ; Evangelisti, C. ; Ferri, P. ; Papa, S. ; Martelli, A.M. ; Falcieri, E.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
Some neuromuscular disorders, such as
Duchenne muscular dystrophy, hereditary inclusion body
myopathy, malignant hyperthermia, alcoholic myopathy
and mitochondrial myopathies are characterized by
oxidative stress and loss of muscle fibres due to
apoptosis. In this study we have analyzed muscle cell
death in vitro utilizing C2C12 myoblasts and myotubes,
inducing apoptosis by means of UVB irradiation. C2C12
cells were analysed by scanning and transmission
electron microscopy (SEM, TEM) as well as by TUNEL
reaction. DNA analysis was performed by gel
electrophoresis and flow cytometry. MitoTracker red
CMXRos and JC-1 fluorescent probes were also used to
study mitochondrial behavior. Finally, caspase activity
was investigated by means of Western blot, while
caspase-9 and -3 inhibitor effects by means of SEM.
SEM showed the typical membrane blebbing while
TEM revealed the characteristic chromatin condensation.
The TUNEL reaction presented a certain positivity too.
Apoptotic and non-apoptotic nuclei in the same myotube
were identified both by TUNEL and TEM.
Gel electrophoresis never showed oligonucleosomal
DNA fragmentation, in agreement with the cell cycle
analysis performed by flow cytometry which did not
reveal a sharp subdiploid peak. Mitochondrial response
to UVB was later investigated and a decrease in
mitochondrial functionality appeared. Caspase-9 and -3
cleavage, and, consequently, the activation of the
caspase cascade, was also demonstrated by Western blot.
Moreover a decrease in apoptotic cell number was noted
after caspase-9 and-3 inhibitor treatment.
All these results indicated that UVB irradiation
induces apoptosis, both in myoblasts and in myotubes,
the second being more resistant. DNA fragmentation, at
least the nucleosomic type, does not occur. A certain
double-strand cleavage appears in TUNEL analysis, as
well as characteristic ultrastructural changes in
chromatin.
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