The Role of Liver-Derived Insulin-Like Growth Factor-I

• Published in: Endocrine reviews 2009-08, Vol.30 (5), p.494-535
• Main Authors: Ohlsson, Claes, Mohan, Subburaman, Sjögren, Klara, Tivesten, Åsa, Isgaard, Jörgen, Isaksson, Olle, Jansson, John-Olov, Svensson, Johan
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Body Composition; Bone and Bones; Bone and Bones - chemistry; Bone and Bones - metabolism; Bone Development; Bone growth; Bone mass; Bone tumors; chemistry; Cortical bone; Endocrinology and Diabetes; Endokrinologi och diabetes; Fundamental and applied biological sciences. Psychology; Fysiologi; Growth factors; Growth Hormone; Growth Hormone - secretion; Growth hormones; Humans; Insulin; Insulin-Like Growth Factor I; Insulin-Like Growth Factor I - physiology; Insulin-Like Growth Factor I - therapeutic use; Insulin-like growth factors; Liver; Liver - metabolism; Memory tasks; metabolism; Parameter sensitivity; Phenotypes; Physiological effects; Physiology; Redundancy; Secretion; Sexual dimorphism; Spatial analysis; Spatial memory; therapeutic use; Vertebrates: endocrinology
• ISSN: 0163-769X; 1945-7189; 1945-7189
• DOI: 10.1210/er.2009-0010

IGF-I is expressed in virtually every tissue of the body, but with much higher expression in the liver than in any other tissue. Studies using mice with liver-specific IGF-I knockout have demonstrated that liver-derived IGF-I, constituting a major part of circulating IGF-I, is an important endocrine factor involved in a variety of physiological and pathological processes. Detailed studies comparing the impact of liver-derived IGF-I and local bone-derived IGF-I demonstrate that both sources of IGF-I can stimulate longitudinal bone growth. We propose here that liver-derived circulating IGF-I and local bone-derived IGF-I to some extent have overlapping growth-promoting effects and might have the capacity to replace each other (= redundancy) in the maintenance of normal longitudinal bone growth. Importantly, and in contrast to the regulation of longitudinal bone growth, locally derived IGF-I cannot replace (= lack of redundancy) liver-derived IGF-I for the regulation of a large number of other parameters including GH secretion, cortical bone mass, kidney size, prostate size, peripheral vascular resistance, spatial memory, sodium retention, insulin sensitivity, liver size, sexually dimorphic liver functions, and progression of some tumors. It is clear that a major role of liver-derived IGF-I is to regulate GH secretion and that some, but not all, of the phenotypes in the liver-specific IGF-I knockout mice are indirect, mediated via the elevated GH levels. All of the described multiple endocrine effects of liver-derived IGF-I should be considered in the development of possible novel treatment strategies aimed at increasing or reducing endocrine IGF-I activity.