Tilemans D, Andries M, Proost P, Devreese B, Van Beeumen J, Denef C
Department of Molecular Cell Biology, University of Leuven School of Medicine, Belgium.
Endocrinology. 1994 Jul;135(1):168-74. doi: 10.1210/endo.135.1.8013350.
We have previously shown that in reaggregate cell cultures of 14-day-old female rat pituitary, LHRH is capable of stimulating lactotrophs to enter the S-phase of the cell cycle, and that this effect is mediated by paracrine growth factors secreted from gonadotrophs. In the present report we describe the isolation, purification, and chemical characterization of one of these growth factors. Gonadotroph-rich aggregates from 14-day-old female rats were cultured for 6-7 weeks in serum-free and serum albumin-free defined medium in the presence of 0.01 nM LHRH. A total volume of 3.2 liters containing material secreted from 2.5 x 10(8) cells was batchwise concentrated on Sep-Pak C18/125 A cartridges (10 g) and retained molecules ultrafiltrated on Centricon 3 membrane filters [mol wt (M(r)) cut-off, 3 kilodaltons (kDa)]. Material capable of increasing the number of [3H]thymidine ([3H]T)-incorporating lactotrophs in pituitary cell aggregates of 2-week-old rats was isolated by chromatography on two reverse phase HPLC columns, one HPLC gel filtration column, and a final reverse phase HPLC column. A substance was obtained which, on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) under reducing conditions, ran as a single band with an apparent M(r) of 16 kDa. On gel filtration, the apparent M(r) was 11 kDa. N-Terminal amino acid sequence analysis revealed that the substance was a peptide; a sequence of 10 residues was obtained, which was identical to that in the N-terminal part of rat POMC. By electrospray ionization mass spectrometry, six different compounds with slightly different M(r), ranging from 10,796-11,108 daltons, were detected. The latter data suggest that the peptide extends C-terminally at least to residue 74, which in the POMC sequence is flanked by an Arg-Arg dibasic residue, a posttranslational cleavage site. The substance increased the number of [3H]T-incorporating lactotrophs in pituitary cell aggregates without affecting [3H]T labeling of other pituitary cell types. Authentic human POMC-(1-76), at a concentration of 10 nM provoked a similar stimulation of the [3H]T-labeled lactotroph number without affecting other cell types. It is concluded that POMC-(1-74) is a growth factor that specifically targets lactotrophs during postnatal development of the rat anterior pituitary.
我们先前已经表明,在14日龄雌性大鼠垂体的再聚集细胞培养物中,促性腺激素释放激素(LHRH)能够刺激催乳细胞进入细胞周期的S期,并且这种作用是由促性腺细胞分泌的旁分泌生长因子介导的。在本报告中,我们描述了其中一种生长因子的分离、纯化和化学特性。将来自14日龄雌性大鼠的富含促性腺细胞的聚集体在无血清和无血清白蛋白的限定培养基中,于0.01 nM LHRH存在下培养6 - 7周。将含有从2.5×10⁸个细胞分泌的物质的总体积为3.2升的溶液分批浓缩在Sep - Pak C18/125 A柱(10 g)上,并将保留的分子在Centricon 3膜过滤器[分子量(M(r))截留值,3千道尔顿(kDa)]上进行超滤。通过在两根反相高效液相色谱(HPLC)柱、一根HPLC凝胶过滤柱和一根最终的反相HPLC柱上进行色谱分离,分离出能够增加2周龄大鼠垂体细胞聚集体中[³H]胸腺嘧啶核苷([³H]T)掺入的催乳细胞数量的物质。得到一种物质,在还原条件下进行十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)时,呈现为一条单一的条带,表观M(r)为16 kDa。在凝胶过滤中,表观M(r)为11 kDa。N端氨基酸序列分析表明该物质是一种肽;获得了一个10个残基的序列,与大鼠阿黑皮素原(POMC)N端部分的序列相同。通过电喷雾电离质谱法,检测到六种不同的化合物,其M(r)略有不同,范围为10,796 - 11,108道尔顿。后一组数据表明该肽的C端至少延伸到第74位残基,在POMC序列中该残基两侧是一个精氨酸 - 精氨酸双碱性残基,这是一个翻译后切割位点。该物质增加了垂体细胞聚集体中[³H]T掺入的催乳细胞数量,而不影响其他垂体细胞类型的[³H]T标记。浓度为10 nM的 authentic human POMC-(1 - 76)对[³H]T标记的催乳细胞数量产生类似的刺激作用,而不影响其他细胞类型。得出的结论是,POMC-(1 - 74)是一种在大鼠垂体前叶产后发育过程中特异性作用于催乳细胞的生长因子。