12 research outputs found
An ultrastructural approach to the study of apoptotic double strand DNA cleavage
Apoptotic DNA cleavage initially produces large fragments (50 kbp), followed by the formation of nucleosomic/ oligonucleosomic ones. On the other hand, apoptosis without DNA fragmentation, at least the nucleosomic one, has
been described. To study the correlation between the DNA
cleavage and the well known chromatin behavior, we
applied TUNEL to electron microscopy, by using a gold-conjugated antidigoxigenin antibody, on U937 and Molt-4 cells, both exposed to UVB or staurosporine. Gold particle density in the different domains of apoptotic nuclei was statistically evaluated. Gold labelling was more intense in dense apoptotic chromatin than in the diffuse one. U937 cells, which evidenced in vitro oligonucleosomic fragmentation after
both treatments, revealed a signiïŹcantly higher gold particle
density, when compared with Molt-4, which did not, even if
showing larger DNA fragments in vitro. DNA fragment sizes,
characterized by gel electrophoresis and by FIGE, appeared
closely correlated to gold particle density on apoptotic chromatin domains. TUNEL applied to electron microscopy is an
useful tool to highlight mechanisms underlying apoptotic
chromatin condensation and DNA cleavage pattern
Subcellular localization of Myogenic Regulatory Factors along skeletal muscle development.
Myogenesis is a multistep process controlled by a transcriptional cascade in which myogenesis regulatory factors (MRFs) have a crucial role [1]. MRFs are a family of basic helix-loop-helix proteins, composed by Myo-D, Myf-5, Myogenin and MRF-4 [2]. They are not activated at the same time: in fact, Myo-D and Myf-5 induce differentiation at earlier step, while Myogenin and MRF-4 are important for myotube formation and for myogenic lineage maintenance [2,3]. C2C12 are murine myoblasts derived from satellite cells and their behaviour corresponds to that of progenitor lineage. They are a subclone of C2 myoblast which spontaneously differentiates in culture after serum removal [5]