Kaplan S A
J Pediatr. 1984 Mar;104(3):327-36. doi: 10.1016/s0022-3476(84)81090-2.
Cells are endowed with specific cognitive molecules that function as receptors for hormones, neurotransmitters, and other intercellular messengers. The receptor molecules may be present in the plasma membrane, cytoplasm, or nucleus. When occupied by the messenger, the receptor is coupled to the cellular machinery that responds to the message-bearing molecules. For some hormones the events following attachment of the messenger to the receptor are well known. An example is the generation of cAMP after combination of glucagon with its receptor and the series of steps culminating in activation of phosphorylase. In the case of many other messengers, including insulin, the nature of these coupling steps is not known. Receptors are subject to the regulatory processes of synthesis, degradation, and conformational change; alterations in receptor properties may have significant effects on the qualitative and quantitative responses of the cell to the extracellular messenger. The insulin receptor is located in the plasma membrane, is composed of two pairs of subunits, and has a molecular weight of about 350,000. It is located in cells such as adipocytes, hepatocytes, and skeletal muscle cells as well as in cells not considered to be typical target organ cells. Insulin receptors in nonfetal cells are downregulated by exposure of the cells to high concentrations of insulin. Other factors that regulate insulin binding include muscular exercise, diet, thyroid hormones, glucocorticoids, androgens, estrogens, and cyclic nucleotides. The fetus has high concentrations of insulin receptors in several tissues. These begin to appear early in fetal life and may outnumber those found in adult tissues. Fetal insulin receptors are unusual in that they may not undergo downregulation but may experience the opposite when exposed to insulin in high concentrations. Thus the offspring of a mother with poorly controlled diabetes may be placed in double jeopardy by fetal hyperinsulinemia and augmented insulin binding by the receptors. Many disorders in children and adults are associated with changes in the properties of the insulin receptor. In general, the alterations have been measured in receptor-bearing cells that are readily accessible, such as circulating monocytes and erythrocytes. The receptors on these cells generally reflect the status of receptors on the major target organs of insulin, although exceptions are known, and conclusions drawn from studies of receptors on circulating cells must be made with caution.(ABSTRACT TRUNCATED AT 400 WORDS)
细胞具有特定的认知分子,这些分子作为激素、神经递质和其他细胞间信使的受体发挥作用。受体分子可能存在于质膜、细胞质或细胞核中。当被信使占据时,受体与响应携带信息分子的细胞机制相偶联。对于某些激素,信使与受体结合后的事件是众所周知的。一个例子是胰高血糖素与其受体结合后生成环磷酸腺苷(cAMP),以及最终导致磷酸化酶激活的一系列步骤。对于包括胰岛素在内的许多其他信使而言,这些偶联步骤的性质尚不清楚。受体受到合成、降解和构象变化等调节过程的影响;受体特性的改变可能对细胞对细胞外信使的定性和定量反应产生重大影响。胰岛素受体位于质膜中,由两对亚基组成,分子量约为350,000。它存在于脂肪细胞、肝细胞和骨骼肌细胞等细胞中,也存在于不被视为典型靶器官细胞的细胞中。非胎儿细胞中的胰岛素受体通过将细胞暴露于高浓度胰岛素而下调。调节胰岛素结合的其他因素包括体育锻炼、饮食、甲状腺激素、糖皮质激素、雄激素、雌激素和环核苷酸。胎儿在几个组织中具有高浓度的胰岛素受体。这些受体在胎儿生命早期就开始出现,数量可能超过成年组织中的受体。胎儿胰岛素受体的不同寻常之处在于它们可能不会下调,反而在暴露于高浓度胰岛素时可能会出现相反的情况。因此,患有糖尿病且控制不佳的母亲的后代可能会因胎儿高胰岛素血症和受体增强的胰岛素结合而处于双重危险之中。儿童和成人的许多疾病都与胰岛素受体特性的变化有关。一般来说,这些改变是在易于获取的含受体细胞中测量的,例如循环单核细胞和红细胞。这些细胞上的受体通常反映胰岛素主要靶器官上受体的状态,尽管也有例外情况,并且从循环细胞上受体的研究得出的结论必须谨慎得出。(摘要截短至400字)