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Actin‐containing microprocesses in the fusion of cultured chick myoblasts
Author(s) -
Huang Helena L.,
Singer Robert H.,
Lazarides Elias
Publication year - 1978
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.880010307
Subject(s) - myocyte , actin , egta , biology , calcium , microbiology and biotechnology , biophysics , myogenesis , anatomy , chemistry , organic chemistry
Scanning electron microscopic studies of myoblasts from 11‐to 13‐day‐old chick embryonic breast muscle cultred on collagen‐coated glass coverslips showed six stages of development into multinucleated myotubes: (1) growth of flattened, spread‐out cells for 20–30 hr following initiation of monolayer cultures; (2) extension of microprocesses (1–150 μm) from cells that have become spindle shaped; (3) contact and adherence of microprocesses from adjacent cells; (4) thickening of fused processes; (5) approximation of the cells; and (6) coalescence of the cells to form a spindle‐shaped myotube. When the calcium‐ion concentration in the growth medium was lowered‐either by increasing the concentration of ethylene‐glycol‐bis (aminoethyl ether) N , N' ‐tetraacetate (EGTA) or by decresing the concentration of free calcium ion used‐the number of microprocesses present on the cells was reduced. Presumably, however, these microprocesses could still fuse together, provided that the calciumion concentration was greater than 160 μM. Indirect immunofluorescence assay with actin‐specific antibody indicated that actin is a major component of the myoblasts' microprocesses. Cytochalasin B (5μg/ml) caused the microprocesses to retract within 15 min and the myoblasts to round up and detach from the glass substrate. This was presumably caused by the action of the drug on actin filaments.