Selective developmental regulation of gene expression for insulin-like growth factor-binding proteins in mouse spinal cord

被引:10
作者
Arnold, PM
Ma, JXY
Citron, BA
Zoubine, MN
Festoff, BW
机构
[1] Univ Kansas, Med Ctr, Dept Neurol, Kansas City, KS 66103 USA
[2] Dept Vet Affairs Med Ctr, Neurobiol Res Lab, Kansas City, MO USA
[3] Dept Vet Affairs Med Ctr, Spinal Cord Res Lab, Kansas City, MO USA
[4] Univ Kansas, Med Ctr, Dept Surg Neurosurg, Kansas City, KS 66160 USA
关键词
binding proteins; embryogenesis; insulin-like growth factor; neurotrophic; paracrine; regeneration; spinal cord;
D O I
10.1097/00007632-200007150-00005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Design. Prospective, randomized experimental study in mice. Study Objective. To determine whether insulin-like growth factor binding proteins (IGFBPs) are present in mouse spinal cord and, if so, what role they play in its :development. Summary of Background Data. Insulin-like growth factors are well recognized hormonal effecters of growth hormone and are expressed in the mammalian spinal cord. The IGFBPs are a group of six genetically distinct proteins that bind IGFs and modulate their bioactivity. They appear in the brain during development, localize to the neuromuscular junction, and promote motor neuron survival. The benefit of IGF-I in amyotrophic lateral sclerosis ALS and its potential use in preventing motor neuron apoptosis in spinal cord injury dictates that studies of the presence and response of IGFBPs in that tissue be performed. Methods. The IGFBPs in mouse spinal cord were analyzed by Western ligand blot, Western immunoblot, and reverse transcription-polymerase chain reaction at various time points from embryonic day 14 to postnatal day 30. Results. Three IGFBPs with molecular masses of 24, 28, and 32 kDa were found, the latter two being the most prominent. The data indicate that these are IGFBP-4, -5, and -2. Conclusion. Both IGFBP-2 and BP-5 are development tally regulated in mouse spinal cord, with higher levels of those at early embryonic stages indicating their potential role In development of the mouse spinal cord.
引用
收藏
页码:1765 / 1770
页数:6
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