Webster J, Scanlon M F
Baillieres Clin Endocrinol Metab. 1991 Dec;5(4):699-726. doi: 10.1016/s0950-351x(10)80011-4.
Normal growth and secretion in the pituitary gland are dependent upon the co-ordinated action of a large number of extracellular growth factors, neuropeptides and peripheral hormones acting on their respective cellular receptors and via complex intracellular signalling pathways. The pituitary and hypothalamus are exposed to a large number of growth factors, several of which have well-documented effects on secretory function and may act as physiological modulators of pituitary hormone synthesis and release. IGF-I, for example, almost certainly acts as a feedback regulator of GH secretion. Despite well-documented mitogenic effects in other tissues, little is known about the role of these growth factors in normal pituitary cell turnover, compensatory hyperplasia or adenoma formation. There is now good evidence, however, that at least some of the hypothalamic releasing peptides are mitogenic for their respective pituitary cell subpopulations. The aetiology of pituitary tumours remains poorly understood but some appear to develop as a result of somatic mutation. Such mutations could enhance growth by causing altered expression of growth factors or their receptors, or constitutive activation of proteins involved in the intracellular mitogenic signal. Abnormalities have been documented at each of these levels in human pituitary tumours. The identification of an activating point mutation in the alpha subunit of Gs, the stimulatory regulatory peptide of adenylyl cyclase, in a proportion of somatotroph adenomas represents a major advance in our understanding of pituitary tumour pathogenesis. This and other findings may ultimately lead to new therapeutic approaches to the management of pituitary disease.
垂体的正常生长和分泌依赖于大量细胞外生长因子、神经肽和外周激素的协同作用,这些物质作用于各自的细胞受体,并通过复杂的细胞内信号通路发挥作用。垂体和下丘脑会接触到大量生长因子,其中一些对分泌功能具有已充分证明的作用,可能作为垂体激素合成和释放的生理调节剂。例如,胰岛素样生长因子 -I几乎可以肯定地作为生长激素分泌的反馈调节因子。尽管在其他组织中有充分记录的促有丝分裂作用,但对于这些生长因子在正常垂体细胞更新、代偿性增生或腺瘤形成中的作用知之甚少。然而,现在有充分的证据表明,至少一些下丘脑释放肽对其各自的垂体细胞亚群具有促有丝分裂作用。垂体肿瘤的病因仍知之甚少,但有些似乎是由于体细胞突变而发生的。此类突变可能通过导致生长因子或其受体的表达改变,或参与细胞内促有丝分裂信号的蛋白质的组成性激活来促进生长。在人类垂体肿瘤的每个这些层面都有异常记录。在一部分生长激素腺瘤中,腺苷酸环化酶的刺激性调节肽Gs的α亚基中发现激活点突变,这代表了我们对垂体肿瘤发病机制理解的重大进展。这一发现和其他发现最终可能会带来垂体疾病治疗的新方法。