Kelberman Daniel, Dattani Mehul T
Biochemistry, Endocrinology and Metabolism Unit, Institute for Child Health, London, UK.
Ann Med. 2006;38(8):560-77. doi: 10.1080/07853890600994963.
The anterior pituitary gland is a central regulator of growth, reproduction and homeostasis, and is the end-product of a carefully orchestrated pattern of expression of signalling molecules and transcription factors leading to the development of this complex organ secreting six hormones from five different cell types. Naturally occurring and transgenic murine models have demonstrated a role for many of these molecules in the aetiology of combined pituitary hormone deficiency (CPHD). These include the transcription factors HESX1, PROP1, POU1FI, LHX3, LHX4, TBX19 (TPIT), SOX3 and SOX2. The expression pattern of these transcription factors, their interaction with co-factors and their impact on target genes dictate the phenotype that results when the gene encoding the relevant transcription factor is mutated. The highly variable phenotype may consist of isolated hypopituitarism, or more complex disorders such as septo-optic dysplasia (SOD) and holoprosencephaly. Since mutations in any one transcription factor are uncommon, and since the overall incidence of mutations in known transcription factors is low in patients with CPHD, it is clear that many genes remain to be identified, and characterization of these will further elucidate the pathogenesis of these complex conditions, and also shed light on normal pituitary development.
腺垂体是生长、生殖和体内稳态的中枢调节者,是信号分子和转录因子精心编排的表达模式的最终产物,这种表达模式导致了这个复杂器官的发育,该器官从五种不同细胞类型分泌六种激素。自然发生的和转基因小鼠模型已经证明了其中许多分子在联合垂体激素缺乏症(CPHD)病因学中的作用。这些分子包括转录因子HESX1、PROP1、POU1F1、LHX3、LHX4、TBX19(TPIT)、SOX3和SOX2。这些转录因子的表达模式、它们与辅助因子的相互作用以及它们对靶基因的影响决定了编码相关转录因子的基因发生突变时所产生的表型。高度可变的表型可能包括孤立性垂体功能减退,或更复杂的疾病,如视隔发育不良(SOD)和前脑无裂畸形。由于任何一种转录因子的突变都不常见,而且在CPHD患者中已知转录因子的总体突变发生率较低,显然还有许多基因有待鉴定,对这些基因的表征将进一步阐明这些复杂病症的发病机制,也有助于了解垂体的正常发育。