Yakar S, Liu J L, Stannard B, Butler A, Accili D, Sauer B, LeRoith D
Section on Cellular and Molecular Physiology, Molecular and Cellular Endocrinology Branch, National Institutes of Health, Bethesda, MD 20892-1770, USA.
Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7324-9. doi: 10.1073/pnas.96.13.7324.
The somatomedin hypothesis proposed that insulin-like growth factor I (IGF-I) was a hepatically derived circulating mediator of growth hormone and is a crucial factor for postnatal growth and development. To reassess this hypothesis, we have used the Cre/loxP recombination system to delete the igf1 gene exclusively in the liver. igf1 gene deletion in the liver abrogated expression of igf1 mRNA and caused a dramatic reduction in circulating IGF-I levels. However, growth as determined by body weight, body length, and femoral length did not differ from wild-type littermates. Although our model proves that hepatic IGF-I is indeed the major contributor to circulating IGF-I levels in mice it challenges the concept that circulating IGF-I is crucial for normal postnatal growth. Rather, our model provides direct evidence for the importance of the autocrine/paracrine role of IGF-I.
生长调节素假说提出,胰岛素样生长因子I(IGF-I)是一种由肝脏产生的生长激素循环介质,是出生后生长发育的关键因素。为了重新评估这一假说,我们使用Cre/loxP重组系统专门在肝脏中删除了igf1基因。肝脏中igf1基因的缺失消除了igf1 mRNA的表达,并导致循环IGF-I水平显著降低。然而,通过体重、体长和股骨长度确定的生长情况与野生型同窝小鼠并无差异。虽然我们的模型证明肝脏IGF-I确实是小鼠循环IGF-I水平的主要贡献者,但它对循环IGF-I对正常出生后生长至关重要这一概念提出了挑战。相反,我们的模型为IGF-I自分泌/旁分泌作用的重要性提供了直接证据。