Hatfield J M, Allen R G, Stack J, Ronnekleiv O
Department of Biochemistry, Oregon Health Sciences University, Portland 97201.
Dev Biol. 1988 Mar;126(1):164-72. doi: 10.1016/0012-1606(88)90250-3.
We have studied the post-translational processing of POMC-derived peptides during fetal monkey pituitary development using immunoassay and reverse-phase high-performance liquid chromatography (RP HPLC). Whole pituitary glands obtained from Day 50 and 55 fetal monkeys and separated lobes From Day 65 to 155 were extracted, fractionated, and analyzed for beta-melanotropin (beta-MSH), midportion beta-endorphin (beta-EP), and acetylated beta-EP immunoactivity. Separated adult pituitary lobes were analyzed for comparison. At Day 50, POMC-containing cells were located in both the anterior and intermediate pituitary lobes by immunofluorescence staining, the majority of these cells were localized in the anterior lobe. The Day 50 and 55 whole pituitaries contained predominantly beta-lipotropin (beta-LPH), gamma-lipotropin (gamma-LPH), beta-EP(1-31), and 2.2-kda beta-MSH. No acetylated products were found in Day 50 whole pituitary extracts. By Day 55, carboxy-shortened and acetylated beta-EPs were barely detectable in whole pituitary extracts. These forms were more apparent in the Day 65 separated neurointermediate lobe (NIL) extracts, and were similar to adult proportions by Day 80. The adult anterior lobe contained predominantly beta-LPH, beta-EP, and gamma-LPH. Adult NILs contained almost exclusively 2.2-kda beta-MSH, alpha-N-acetyl beta-EP(1-31) and alpha-N-acetyl beta-EP(1-27). The production of 2.2-kda beta-LPH in the monkey NIL indicates that monkey beta-LPH is different from rat beta-LPH in that it must contain the paired-basic cleavage site required for the formation of 2.2-kda beta-MSH that is known to be lacking in rat beta-LPH. Another finding was that monkey beta-EP contains a Tyr residue at position 27 as found in human beta-EP but appears to have the rat Gln substitution at position 31. The post-translational processing patterns characteristic of each lobe were well established by midterm fetal development (Day 80).
我们使用免疫测定法和反相高效液相色谱法(RP HPLC)研究了胎猴垂体发育过程中源自阿片促黑素皮质素原(POMC)的肽的翻译后加工过程。提取了取自妊娠50天和55天胎猴的整个垂体以及取自妊娠65天至155天的分离叶,进行分级分离,并分析其中β-促黑素(β-MSH)、中段β-内啡肽(β-EP)和乙酰化β-EP的免疫活性。对分离的成年垂体叶进行分析以作比较。在妊娠50天时,通过免疫荧光染色发现含POMC的细胞位于垂体前叶和中间叶,其中大多数细胞位于前叶。妊娠50天和55天的整个垂体主要含有β-促脂素(β-LPH)、γ-促脂素(γ-LPH)、β-EP(1 - 31)和2.2 kDa的β-MSH。在妊娠50天的整个垂体提取物中未发现乙酰化产物。到妊娠55天时,羧基缩短和乙酰化的β-EP在整个垂体提取物中几乎检测不到。这些形式在妊娠65天分离的神经中间叶(NIL)提取物中更明显,到妊娠80天时与成年比例相似。成年前叶主要含有β-LPH、β-EP和γ-LPH。成年NIL几乎只含有2.2 kDa的β-MSH、α-N-乙酰基β-EP(1 - 31)和α-N-乙酰基β-EP(1 - 27)。猴NIL中2.2 kDaβ-LPH的产生表明,猴β-LPH与大鼠β-LPH不同,因为它必须含有形成2.2 kDaβ-MSH所需的双碱性裂解位点,而大鼠β-LPH已知缺乏该位点。另一个发现是,猴β-EP在第27位含有一个酪氨酸残基,如同人β-EP,但在第31位似乎具有大鼠的谷氨酰胺替代。每个叶的翻译后加工模式在胎儿中期发育(妊娠80天)时已充分确立。