We investigated the potential of cultured myoblasts to generate skeletal mu
scle in an ectopic site. Myoblasts from a clonal cell line or from expanded
primary cultures were injected under the skin of the lumbar region of adul
t syngenic Balb/c mice. One to 7 weeks after injection, distinct muscles, o
f greater mass in mice injected with clonal myoblasts (6-78 mg, n = 37) tha
n in mice injected with primary myoblasts (1-7 mg, n = 26), had formed betw
een the subcutaneous panniculus carnosus muscle and the trunk muscles of ho
st animals, These ectopic muscles exhibited spontaneous and/or electrically
-evoked contractions after the second week and, when stimulated directly in
vitro, isometric contractile properties similar to those of normal muscles
. Histological, electron microscopical and tissue culture examination of th
ese muscles revealed their largely mature morphology and phenotype. The fib
res, most of which were branched, were contiguous, aligned and capillarised
, exhibited normal sarcormeric protein banding patterns, and expressed musc
le-specific proteins, including desmin, dystrophin, and isoforms of develop
mental and adult myosin heavy chain, Enveloping each fibre was a basal lami
na, beneath which lay quiescent satellite cells, which could be stimulated
to produce new muscle in culture. Presence of endplates (revealed by cc-bun
garotoxin and neurofilament staining), and the eventual loss of expression
of neural cell adhesion molecule and extrasynaptic acetylcholine receptors,
indicated that some fibres were innervated, That these muscle fibres were
of implanted-cell origin was supported by the finding of Y-chromosome and a
lack of dystrophin in ectopic muscles formed after subcutaneous injection
of, respectively, male myoblasts into female mice and dystrophin-deficient
(mdx) myoblasts into normal C57B1/10 muscle, Our results demonstrate that a
n organised, functional muscle can be generated de novo from a disorganised
mass of myoblasts implanted in an extramuscular subcutaneous site, whereby
the host contributes significantly in providing support tissues and innerv
ation, Our observations are also consistent with the idea that myogenic cel
ls behave like tissue-specific stem cells, generating new muscle precursor
(satellite) cells as well as mature muscle. Subcutaneous implantation of my
oblasts may have a range of useful applications, from the study of myogenes
is to the delivery of gene products.