Insulin-like Growth Factor 1 Signaling in Mammalian Hearing

被引:16
|
作者
Garcia-Mato, Angela [1 ,2 ]
Cervantes, Blanca [1 ,2 ]
Murillo-Cuesta, Silvia [1 ,2 ,3 ]
de la Rosa, Lourdes [2 ,3 ]
Varela-Nieto, Isabel [1 ,2 ,3 ]
机构
[1] Univ Madrid CSIC UAM, Inst Biomed Res Alberto Sols IIBm, Spanish Natl Res Council, Madrid 28029, Spain
[2] CIBER, Rare Dis Networking Biomed Res Ctr CIBERER, Carlos Inst Hlth 3, Madrid 28029, Spain
[3] Paz Hosp Inst Hlth Res IdiPAZ, Madrid 28046, Spain
基金
欧盟地平线“2020”;
关键词
Ageing; AKT; GH; IGF1; mutations; IGF system; inner ear; hearing loss; neurodegeneration; RAF; rare diseases; PROTEIN-KINASE; SHORT STATURE; HORMONE TREATMENT; BINDING-PROTEINS; MOUSE MUTANTS; IGF2; MUTATION; INNER-EAR; GENE; EXPRESSION; ACTIVATION;
D O I
10.3390/genes12101553
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Insulin-like growth factor 1 (IGF-1) is a peptide hormone belonging to the insulin family of proteins. Almost all of the biological effects of IGF-1 are mediated through binding to its high-affinity tyrosine kinase receptor (IGF1R), a transmembrane receptor belonging to the insulin receptor family. Factors, receptors and IGF-binding proteins form the IGF system, which has multiple roles in mammalian development, adult tissue homeostasis, and aging. Consequently, mutations in genes of the IGF system, including downstream intracellular targets, underlie multiple common pathologies and are associated with multiple rare human diseases. Here we review the contribution of the IGF system to our understanding of the molecular and genetic basis of human hearing loss by describing, (i) the expression patterns of the IGF system in the mammalian inner ear; (ii) downstream signaling of IGF-1 in the hearing organ; (iii) mouse mutations in the IGF system, including upstream regulators and downstream targets of IGF-1 that inform cochlear pathophysiology; and (iv) human mutations in these genes causing hearing loss.</p>
引用
收藏
页数:22
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