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Targeted Expression of IGF‐1 Transgene to Skeletal Muscle Accelerates Muscle and Motor Neuron Regeneration
Author(s) -
Rabinovsky Eric D.,
Gelir Ethem,
Gelir Seda,
Lui Hui,
Kattash Maan,
DeMayo Francesco J.,
Shenaq Saleh M.,
Schwartz Robert J.
Publication year - 2003
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.02-0183fje
Subject(s) - myogenin , myod , skeletal muscle , transgene , regeneration (biology) , biology , genetically modified mouse , microbiology and biotechnology , myocyte , neuromuscular junction , medicine , endocrinology , myogenesis , neuroscience , gene , genetics
ABSTRACT Currently, there is no known medical treatment that hastens the repair of damaged nerve and muscle. Using IGF‐1 transgenic mice that specifically express human recombinant IGF‐1 in skeletal muscle, we test the hypotheses that targeted gene expression of IGF‐1 in skeletal muscle enhances motor nerve regeneration after a nerve crush injury. The IGF‐1 transgene affects the initiation of the muscle repair process after nerve injury as shown by increased activation of SCA‐1positive myogenic stem cells. Increased satellite cell differentiation and proliferation are observed in IGF‐1 transgenic mice, shown by increased expression of Cyclin D1, MyoD, and myogenin. Expression of myogenin and nicotinic acetylcholine receptor subunits, initially increased in both wild‐type and IGF‐1 transgenic mice, are restored to normal levels at a faster rate in IGF‐1 transgenic mice, which indicates a rescue of nerve‐evoked muscle activity. Expression of the IGF‐1 transgene in skeletal muscle results in accelerated recovery of saltatory nerve conduction, increased innervation as detected by neurofilament expression, and faster recovery of muscle mass. These studies demonstrate that local expression of IGF‐1 augments the repair of injured nerve and muscle.