Molecular and cell biology of skeletal muscle regeneration.
Molecular and cell biology of skeletal muscle regeneration.
复制标题
DOI:
10.1007/978-94-011-1528-5_9
复制
发表时间:
1993
期刊:
影响因子:
--
通讯作者:
M. Grounds;Z. Yablonka-Reuveni
中科院分区:
文献类型:
--
作者:
M. Grounds;Z. Yablonka-Reuveni
When skeletal muscle is damaged, it is repaired by the proliferation of mononuclear muscle precursor cells (mpc) which fuse either with one another to form young multinucleated muscle cells (myotubes) or with the ends of damaged myofibres (Robertsonet al., 1990). The success of new muscle formation is related to the size of the injury, as after major trauma and extensive disruption of the external lamina of muscle fibres there is often significant replacement by fibrous and cellular connective tissue. Impaired muscle regeneration and progressive replacement by fat and connective tissue is a feature of myopathies such as Duchenne muscular dystrophy (DMD), although this results from many small discrete lesions constantly recurring over a long period of time rather than from a single large injury. Failed regeneration can be seen in simplistic terms as a failure of muscle precursor replication. In this review we shall concentrate on the biology of muscle precursor cells. For coverage of other aspects of regeneration such as resealing of damaged myofibres, revascularization and reinnervation, see Grounds (1991).