We have studied the fusion process of myoblasts in the mytome correspo
nding to H.H. stages 22, 23 and 24 from calcitonin-treated chick embry
os and their untreated controls. The micrograph images of this process
were studied to detect the ultrastructural changes in myoblast morpho
logy that could be associated with the known hormonal and biochemical
changes that take place in preparation of fusion. Once actin and myosi
n myofilament differentiation and sarcomerogenesis had begun, the myot
ome myoblasts fused in bundles of 10-14 myoblasts, and the following w
as observed during this process: plasmatic membrane interdigitation an
d invagination; the appearance of cytoplasmic flaps covering other myo
blasts and fading at the point of contact; plasmatic membranes that fa
de and disintegrate; membrane rupturing; double closed lamina; small r
inged lamina; large disperse vesicles; small vesicles (liposomes), and
semi-dense amorphous material. Seven stages were established: 1.- Mem
brane rupture; 2.- Double closed and elongated lamina; 3.- Small ringe
d lamina aligned lengthwise; 4.- Large dispersed vesicles; 5.- Impreci
se boundaries with amorphous material in diffuse areas; 6.- Cytoplasm
fusion; and 7.- Prefunctional syncitium. Answers to the questions: <<h
ow>>, <<when>>, <<where>>, <<why>> and <<for what purpose>> the fusion
of myoblasts takes place are suggested.