Katayama T, Furuya M, Yamaichi K, Konishi K, Sugiura N, Murafuji H, Magota K, Saito M, Tanaka S, Oikawa S
Suntory Biomedical Research Limited, 1-1-1 Wakayamadai, Shimamoto-cho, Mishima-gun, 618-8503, Osaka, Japan.
Biochim Biophys Acta. 2001 May 3;1526(2):183-90. doi: 10.1016/s0304-4165(01)00125-8.
Calcitonin (CT), a 32-amino acid peptide hormone secreted mainly from the thyroid gland, plays an important role in maintaining bone homeostasis. To discover non-peptide small molecules with biological actions similar to those of CT, a cell-based screening of an in-house chemical library was performed and a pyridone derivative (SUN B8155) was identified. Like CT, it elevated cyclic AMP (cAMP) levels in T47D and UMR106-06 cells which endogenously express human and rat CT receptor, respectively. SUN B8155 also stimulated cAMP formation in cells expressing recombinant human CT receptor, but not in those expressing human parathyroid hormone/parathyroid hormone-related peptide receptor. Accumulation of cAMP in T47D cells was blocked by a selective antagonist of CT receptor, salmon CT(8-32), whereas SUN B8155 did not displace the specific binding of [(125)I]CT to the receptor. Our results suggested that the compound selectively interacts with the CT receptor by a mechanism similar to but probably different from that of CT itself. In rats, intraperitoneal administration of SUN B8155 significantly lowered serum calcium levels, like CT. Our results demonstrate, for the first time, that the biological activities of the newly identified small molecule can mimic that of CT, acting via the CT receptor.
降钙素(CT)是一种主要由甲状腺分泌的含32个氨基酸的肽类激素,在维持骨骼稳态中发挥重要作用。为了发现具有与CT相似生物学作用的非肽小分子,我们对内部化学文库进行了基于细胞的筛选,并鉴定出一种吡啶酮衍生物(SUN B8155)。与CT一样,它分别在内源性表达人和大鼠CT受体的T47D和UMR106 - 06细胞中提高了环磷酸腺苷(cAMP)水平。SUN B8155还能刺激表达重组人CT受体的细胞中cAMP的形成,但对表达人甲状旁腺激素/甲状旁腺激素相关肽受体的细胞无此作用。CT受体的选择性拮抗剂鲑鱼降钙素(8 - 32)可阻断T47D细胞中cAMP的积累,而SUN B8155不会取代[(125)I]CT与受体的特异性结合。我们的结果表明,该化合物通过一种与CT本身相似但可能不同的机制与CT受体选择性相互作用。在大鼠中,腹腔注射SUN B8155与CT一样能显著降低血清钙水平。我们的结果首次证明,新鉴定的小分子的生物学活性可以模拟CT,通过CT受体发挥作用。