Redei E, Hilderbrand H, Aird F
Department of Pharmacology, University of Pennsylvania, Philadelphia 19104, USA.
Endocrinology. 1995 Aug;136(8):3557-63. doi: 10.1210/endo.136.8.7628393.
ACTH is the major regulator of the body's adaptive response to stress and the physiological stimulus for glucocorticoid secretion. In addition to the known negative feedback regulation of ACTH by glucocorticoids, a hypothalamic corticotropin release-inhibiting factor (CRIF) that inhibits ACTH synthesis and secretion has been postulated, but not identified. We previously reported that transfection of prepro-TRH complementary DNA into the mouse anterior pituitary tumor cell line AtT-20 results in inhibition of basal and corticotropin-releasing hormone (CRH)-stimulated ACTH synthesis and secretion, suggesting that one or more of the cryptic peptides encoded within the prepro-TRH precursor has CRIF activity. To narrow the choice of peptides responsible for CRIF activity, we first deleted specific sequences within the prepro-TRH complementary DNA and transfected these constructs into AtT-20 cells. Deletion of sequences encoding amino acids 119-229 resulted in the loss of CRIF activity. Of the peptides encoded within this region, prepro-TRH-(178-199), a 22-amino acid peptide, inhibited basal and CRH-stimulated ACTH synthesis and secretion in cultured primary anterior pituitary cells. As this peptide is processed from prepro-TRH in vivo, is found in the external zone of the median eminence, and is secreted from hypothalamic slices in vitro, prepro-TRH-(178-199) fulfills the criteria for a physiological CRIF. The significance of TRH and CRIF sharing a common precursor opens new areas of research in the integrated regulation of pituitary-adrenal and pituitary-thyroid functions.
促肾上腺皮质激素(ACTH)是机体对应激产生适应性反应的主要调节因子,也是糖皮质激素分泌的生理刺激物。除了已知的糖皮质激素对ACTH的负反馈调节外,人们推测存在一种抑制ACTH合成和分泌的下丘脑促肾上腺皮质激素释放抑制因子(CRIF),但尚未确定。我们之前报道,将前促甲状腺激素释放激素(prepro-TRH)互补DNA转染到小鼠垂体前叶肿瘤细胞系AtT-20中,会抑制基础状态下以及促肾上腺皮质激素释放激素(CRH)刺激下的ACTH合成和分泌,这表明前促甲状腺激素释放激素前体中编码的一种或多种潜在肽段具有CRIF活性。为了缩小负责CRIF活性的肽段范围,我们首先删除了前促甲状腺激素释放激素互补DNA中的特定序列,并将这些构建体转染到AtT-20细胞中。删除编码氨基酸119 - 229的序列会导致CRIF活性丧失。在该区域编码的肽段中,一种22个氨基酸的肽段前促甲状腺激素释放激素-(178 - 199),可抑制原代培养垂体前叶细胞基础状态下以及CRH刺激下的ACTH合成和分泌。由于这种肽段在体内是从前促甲状腺激素释放激素加工而来,存在于正中隆起的外侧区,并且在体外可从下丘脑切片中分泌,所以前促甲状腺激素释放激素-(178 - 199)符合生理性CRIF的标准。促甲状腺激素释放激素(TRH)和CRIF共享一个共同前体的意义,为垂体-肾上腺和垂体-甲状腺功能的整合调节开辟了新的研究领域。