Goldfine Ira D, Maddux Betty A, Youngren Jack F, Reaven Gerald, Accili Domenico, Trischitta Vincenzo, Vigneri Riccardo, Frittitta Lucia
Department of Medicine and Diabetes Center, University of California San Francisco, San Francisco, California 94143, USA.
Endocr Rev. 2008 Feb;29(1):62-75. doi: 10.1210/er.2007-0004. Epub 2008 Jan 16.
Insulin resistance is a major feature of most patients with type 2 diabetes mellitus (T2D). A number of laboratories have observed that PC-1 (membrane [corrected] glycoprotein plasma cell antigen 1; also termed [corrected] ectonucleotide pyrophosphatase phosphodiesterase 1 or ENPP1) [corrected] is either overexpressed or overactive in muscle, adipose tissue, fibroblasts, and other tissues of insulin-resistant individuals, both nondiabetic and diabetic. Moreover, PC-1 (ENPP1) overexpression [corrected] in cultured cells in vitro and in transgenic mice in vivo, [corrected] impairs insulin stimulation of insulin receptor (IR) activation and downstream signaling. PC-1 binds to the connecting domain of the IR alpha-subunit that is located in residues 485-599. The connecting domain transmits insulin binding in the alpha-subunit to activation of tyrosine kinase activation in the beta-subunit. When PC-1 is overexpressed, it inhibits insulin [corrected]induced IR beta-subunit tyrosine kinase activity. In addition, a polymorphism of PC-1 (K121Q) in various ethnic populations is closely associated with insulin resistance, T2D, and cardio [corrected] and nephrovascular diseases. The product of this polymorphism has a 2- to 3-fold increased binding affinity for the IR and is more potent than the wild-type PC-1 protein (K121K) in inhibiting the IR. These data suggest therefore that PC-1 is a candidate protein that may play a role in human insulin resistance and T2D by its overexpression, its overactivity, or both.
胰岛素抵抗是大多数2型糖尿病(T2D)患者的主要特征。许多实验室观察到,PC-1(膜糖蛋白浆细胞抗原1;也称为外核苷酸焦磷酸酶磷酸二酯酶1或ENPP1)在胰岛素抵抗个体(包括非糖尿病和糖尿病个体)的肌肉、脂肪组织、成纤维细胞和其他组织中要么过度表达,要么活性过高。此外,PC-1(ENPP1)在体外培养细胞和体内转基因小鼠中的过度表达会损害胰岛素对胰岛素受体(IR)激活和下游信号传导的刺激。PC-1与位于485-599位残基的IRα亚基的连接结构域结合。连接结构域将α亚基中的胰岛素结合传递至β亚基中酪氨酸激酶激活的激活。当PC-1过度表达时,它会抑制胰岛素诱导的IRβ亚基酪氨酸激酶活性。此外,PC-1(K121Q)在不同种族人群中的多态性与胰岛素抵抗、T2D以及心血管和肾血管疾病密切相关。这种多态性的产物对IR的结合亲和力增加了2至3倍,并且在抑制IR方面比野生型PC-1蛋白(K121K)更有效。因此,这些数据表明PC-1是一种候选蛋白,可能通过其过度表达、过度活性或两者在人类胰岛素抵抗和T2D中发挥作用。