Noel G, Mains R E
Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
Endocrinology. 1991 Sep;129(3):1317-25. doi: 10.1210/endo-129-3-1317.
Compared to corticotropes in the adult rat anterior pituitary, neonatal corticotropes exhibit a significantly lower extent of conversion of precursor molecules into ACTH and a substantially greater extent of ACTH cleavage into smaller product peptides similar in size to alpha-melanotropin and corticotropin-like intermediate lobe peptide (CLIP). In the present study we examined pro-ACTH/endorphin (PAE; also called POMC) processing in corticotropes at different times during postnatal development to determine when these cells cease cleaving ACTH into smaller peptides and when they cease accumulating large amounts of intact precursor in vivo. The pattern of processing observed in the newborn is maintained through the second week after birth. A dramatic decrease in ACTH cleavage occurs between the second and third postnatal weeks. The extent of precursor cleavage increases toward the adult pattern by the fifth postnatal week. Explants of newborn anterior pituitary were previously shown to exhibit increased cleavage of ACTH into ACTH-(1-13)NH2 and CLIP, a process that was suppressed by glucocorticoids. To determine whether corticotropes from older animals maintained this plasticity and what intercellular interactions might be required, dissociated primary cultures were maintained in complete serum-free medium with or without added glucocorticoids. After 7 days in complete serum-free medium, the cellular content of both intact precursor and peptides the size of CLIP was increased compared to the corresponding in vivo pattern for animals from birth through adulthood. Although corticotropes from younger animals exhibited more pronounced changes when placed in culture, even cultures from adult animals exhibited some ACTH cleavage. For corticotrope cultures prepared from animals up to postnatal day 15, chronic treatment with dexamethasone did not suppress ACTH cleavage activity, although glucocorticoids did suppress ACTH cleavage in cultures from animals older than postnatal day 22. Biosynthetic labeling studies with cultures from 4- to 5-week-old rats demonstrated that the powerful suppressive effect of dexamethasone on the cleavage of newly synthesized ACTH-(1-39) was only evident 24 h after addition of the glucocorticoid to the culture medium. In contrast, removal of dexamethasone allowed cleavage of ACTH to commence within a few hours.
与成年大鼠垂体前叶的促肾上腺皮质激素细胞相比,新生促肾上腺皮质激素细胞将前体分子转化为促肾上腺皮质激素(ACTH)的程度显著较低,而将ACTH裂解为与α-促黑素和促肾上腺皮质激素样中叶肽(CLIP)大小相似的较小产物肽的程度则显著更高。在本研究中,我们检测了出生后不同发育阶段促肾上腺皮质激素细胞中前体ACTH/内啡肽(PAE;也称为阿黑皮素原,POMC)的加工过程,以确定这些细胞何时停止将ACTH裂解为较小的肽,以及何时停止在体内积累大量完整的前体。在新生动物中观察到的加工模式在出生后的第二周内保持不变。出生后第二周和第三周之间,ACTH裂解显著减少。到出生后第五周,前体裂解程度朝着成年模式增加。先前已证明,新生垂体前叶外植体中ACTH裂解为ACTH-(1-13)NH2和CLIP的过程会增加,而该过程会受到糖皮质激素的抑制。为了确定来自年龄较大动物的促肾上腺皮质激素细胞是否保持这种可塑性以及可能需要何种细胞间相互作用,将原代解离培养物置于添加或不添加糖皮质激素的完全无血清培养基中。在完全无血清培养基中培养7天后,与从出生到成年动物的相应体内模式相比,完整前体和CLIP大小的肽的细胞含量均增加。尽管来自较年轻动物的促肾上腺皮质激素细胞在培养时表现出更明显的变化,但即使是来自成年动物的培养物也表现出一些ACTH裂解。对于出生后第15天之前动物制备的促肾上腺皮质激素细胞培养物,地塞米松的长期处理并未抑制ACTH裂解活性,尽管糖皮质激素确实抑制了出生后第22天之后动物培养物中的ACTH裂解。对4至5周龄大鼠培养物进行的生物合成标记研究表明,地塞米松对新合成的ACTH-(1-39)裂解的强大抑制作用仅在向培养基中添加糖皮质激素24小时后才明显。相反,去除地塞米松后,ACTH的裂解在数小时内即可开始。