Van Bael A, Seuntjens E, Proesmans M, Denef C
Laboratory of Cell Pharmacology, University of Leuven, School of Medicine, Campus Gasthuisberg, Belgium.
J Neuroendocrinol. 1998 Jun;10(6):437-45. doi: 10.1046/j.1365-2826.1998.00205.x.
Reverse transcription-polymerase chain reaction (RT-PCR) with specific GnRH cDNA primers performed on RNA from Rathke's pouches removed from pregnant rats at day 12 of gestation (e12) generated an amplified DNA fragment of the expected length (357 bp). The fragment hybridized with a labeled GnRH cDNA probe in Southern blotting. DNA sequencing demonstrated identity with the known nucleotide sequence of the corresponding segment of rat GnRH cDNA. To determine whether GnRH mRNA was located in the Rathke's pouch cells or in remnants of surrounding tissue not completely removed during preparation, the pouches were treated with collagenase. Based on light and electron microscopic examination, this treatment disconnected virtually all contaminating tissue, allowing the 'pure' Rathke's pouches to be picked-up separately. Again, RT-PCR generated a DNA fragment of the expected length, the fragment hybridized with the GnRH cDNA probe and showed the nucleotide sequence of the corresponding region of rat GnRH cDNA. In Rathke's pouches established in explant culture on e12, lactotrophs were well developed when examined 9 days later by immunostaining of prolactin in paraffin-embedded sections of the tissue. Computerized image analysis showed prolactin immunoreactivity in 8.0+/-1.1% of the section area. Addition of the potent and long-acting GnRH antagonist ORG 30276 to the crude preparation of Rathke's pouches caused a significant decrease in the relative area staining for prolactin. The latter effect was abolished by concomitant addition of GnRH. In preparations of pure Rathke's pouches (collagenase-treated), ORG 30276 failed to affect the relative area of prolactin immunoreactivity. GnRH mRNA remained expressed in explants of both crude and pure Rathke's pouches until the end of the culture period. It is concluded that the GnRH gene is expressed in Rathke's pouch as early as e12 and that GnRH may be a physiological paracrine/autocrine peptide stimulating the development of lactotrophs. Mesenchymal and/or neural factors may be essential for the latter system to function.
用特异性促性腺激素释放激素(GnRH)互补DNA(cDNA)引物对妊娠第12天(e12)的孕鼠切除的拉特克囊RNA进行逆转录-聚合酶链反应(RT-PCR),产生了预期长度(357碱基对)的扩增DNA片段。该片段在Southern印迹中与标记的GnRH cDNA探针杂交。DNA测序显示与大鼠GnRH cDNA相应片段的已知核苷酸序列相同。为了确定GnRH信使核糖核酸(mRNA)是位于拉特克囊细胞中还是位于制备过程中未完全去除的周围组织残余物中,对这些囊进行了胶原酶处理。基于光镜和电镜检查,这种处理几乎分离了所有污染组织,使得能够分别挑出“纯净”的拉特克囊。同样,RT-PCR产生了预期长度的DNA片段,该片段与GnRH cDNA探针杂交,并显示出大鼠GnRH cDNA相应区域的核苷酸序列。在e12建立的外植体培养的拉特克囊中,9天后通过对组织石蜡包埋切片中的催乳素进行免疫染色检查发现,催乳细胞发育良好。计算机图像分析显示,催乳素免疫反应性占切片面积的8.0±1.1%。向拉特克囊粗制品中添加强效长效GnRH拮抗剂ORG 30276导致催乳素相对染色面积显著减少。同时添加GnRH可消除后一种作用。在纯净的拉特克囊(胶原酶处理)制品中,ORG 30276未能影响催乳素免疫反应性的相对面积。直到培养期结束,GnRH mRNA在粗制和纯净拉特克囊的外植体中均持续表达。得出的结论是,GnRH基因早在e12就在拉特克囊中表达,并且GnRH可能是一种刺激催乳细胞发育的生理性旁分泌/自分泌肽。间充质和/或神经因子对于后一种系统发挥功能可能至关重要。