Bach M A, Bondy C A
Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Endocrinology. 1992 Dec;131(6):2588-94. doi: 10.1210/endo.131.6.1280202.
In situ hybridization was used to map patterns of gene expression for components of the insulin-like growth factor (IGF) system, including IGF-I and -II, IGF-binding proteins 1-5 (IGFBP1-5), the IGF-I receptor, and GH in the rat pituitary. IGF-I mRNA was concentrated in isolated cells scattered throughout the gland with features typical of nonendocrine folliculo-stellate cells. IGF-II mRNA was abundant in neural (NL) and intermediate lobe (IL) capillaries, and low levels were present in endocrine cells of anterior lobe (AL) and IL. IGFBP1 mRNA was not detected in the pituitary. IGFBP2 mRNA was concentrated in epithelial cells lining AL follicles and in astroglial-like cells (pituicytes) of the NL. IGFBP3 mRNA was localized in isolated cells scattered throughout the AL and NL. IGFBP4 mRNA was relatively abundant in NL pituicytes and was diffusely expressed in the AL. IGFBP5 mRNA was equally abundant in NL and AL, and was localized in folliculo-stellate and epithelial cells of the AL and pituicytes and capillaries of the NL. Neither IGF-I nor IGFBP1-5 were detected in the IL. IGF-I receptor mRNA was abundant and homogeneously distributed throughout the AL and IL, compatible with expression by endocrine cells. There was overlap, but no particular correlation, between IGF system gene expression and GH-producing cells, which were clustered in the dorsal-lateral wings of the AL. In summary, IGF system gene expression is bountiful in the rat pituitary, but does not correlate with sites of GH synthesis. IGF-I receptor mRNA, which might have been expected to localize to somatotrophs, appears to be equally abundant in all of the endocrine cells of both AL and IL; the other constituents of the IGF system are localized in connective tissue and support elements that demonstrate no special anatomical relationship to somatotrophs. Finally, there is remarkably abundant gene expression for IGFBP2, -4, and -5 in the NL.
原位杂交技术被用于绘制大鼠垂体中胰岛素样生长因子(IGF)系统各成分的基因表达模式,这些成分包括IGF-I和-II、IGF结合蛋白1 - 5(IGFBP1 - 5)、IGF-I受体以及生长激素(GH)。IGF-I mRNA集中在散布于整个腺体的孤立细胞中,这些细胞具有非内分泌性滤泡星状细胞的典型特征。IGF-II mRNA在前叶(AL)和中间叶(IL)的神经(NL)毛细血管中丰富,而在前叶和中间叶的内分泌细胞中含量较低。垂体中未检测到IGFBP1 mRNA。IGFBP2 mRNA集中在AL滤泡内衬的上皮细胞以及NL的星形胶质样细胞(垂体细胞)中。IGFBP3 mRNA定位于散布在整个AL和NL的孤立细胞中。IGFBP4 mRNA在NL垂体细胞中相对丰富,并在前叶中呈弥散性表达。IGFBP5 mRNA在NL和AL中同样丰富,定位于AL的滤泡星状细胞和上皮细胞以及NL的垂体细胞和毛细血管中。在IL中未检测到IGF-I和IGFBP1 - 5。IGF-I受体mRNA丰富且均匀地分布于整个AL和IL,这与内分泌细胞的表达情况相符。IGF系统基因表达与产生GH的细胞之间存在重叠,但无特定相关性,产生GH的细胞聚集在AL的背外侧翼。总之,IGF系统基因表达在大鼠垂体中丰富,但与GH合成部位无关。IGF-I受体mRNA本应定位于生长激素细胞,但在AL和IL的所有内分泌细胞中似乎同样丰富;IGF系统的其他成分定位于结缔组织和支持元件中,这些与生长激素细胞没有特殊的解剖学关系。最后,NL中IGFBP2、-4和-5的基因表达非常丰富。